- Research article
- Open Access
Integration of tomato reproductive developmental landmarks and expression profiles, and the effect of SUN on fruit shape
BMC Plant Biology volume 9, Article number: 49 (2009)
Universally accepted landmark stages are necessary to highlight key events in plant reproductive development and to facilitate comparisons among species. Domestication and selection of tomato resulted in many varieties that differ in fruit shape and size. This diversity is useful to unravel underlying molecular and developmental mechanisms that control organ morphology and patterning. The tomato fruit shape gene SUN controls fruit elongation. The most dramatic effect of SUN on fruit shape occurs after pollination and fertilization although a detailed investigation into the timing of the fruit shape change as well as gene expression profiles during critical developmental stages has not been conducted.
We provide a description of floral and fruit development in a red-fruited closely related wild relative of tomato, Solanum pimpinellifolium accession LA1589. We use established and propose new floral and fruit landmarks to present a framework for tomato developmental studies. In addition, gene expression profiles of three key stages in floral and fruit development are presented, namely floral buds 10 days before anthesis (floral landmark 7), anthesis-stage flowers (floral landmark 10 and fruit landmark 1), and 5 days post anthesis fruit (fruit landmark 3). To demonstrate the utility of the landmarks, we characterize the tomato shape gene SUN in fruit development. SUN controls fruit shape predominantly after fertilization and its effect reaches a maximum at 8 days post-anthesis coinciding with fruit landmark 4 representing the globular embryo stage of seed development. The expression profiles of the NILs that differ at sun show that only 34 genes were differentially expressed and most of them at a less than 2-fold difference.
The landmarks for flower and fruit development in tomato were outlined and integrated with the effect of SUN on fruit shape. Although we did not identify many genes differentially expressed in the NILs that differ at the sun locus, higher or lower transcript levels for many genes involved in phytohormone biosynthesis or signaling as well as organ identity and patterning of tomato fruit were found between developmental time points.
Plants display a diverse array of shapes, sizes and categories of fruit. Within the Solanaceae family fruit categories range from capsules, drupes, pyrenes, berries, to several other types of non-capsular dehiscent fruits . Within one species such as tomato (Solanum lycopersicum L.), fruit morphology varies dramatically among cultivated accessions. The dramatic diversity in tomato fruit shape and size is due to domestication and continued selection for its fruit characters [2, 3]. Fruit formation starts with the development of the floral meristem. Within the floral meristem, the expression of organ identity genes gives rise to the four whorls namely the sepals, petals, stamen and gynoecium. The coordinate spatial and temporal expression of several classes of homeotic genes specifies the identity of floral organs [4–7]. A class genes control sepal identity, A and B class genes specify the identity of petals, B and C genes define stamen identity, and C genes control carpel identity. The E class genes act redundantly in specifying the identity of floral whorls in combinations with the A, B and C genes [5–7].
After organ specification within the floral meristem, a complex growth patterning is observed in the fourth floral whorl comprising the gynoecium, which will become the fruit after fertilization of the ovules. Along the apical-basal axis, the developing tissue types of the gynoecium are the stigma, style, ovary and gynophore, whereas along the mediolateral axis of the ovary the valves or pericarp, septum or columella, placenta and ovules are formed. In fruit such as that of Arabidopsis, the gynoecium also includes two dehiscence-related tissues, replum and valve margin [8, 9]. Combined with the organ and tissue identity genes, patterning is controlled by the expression of genes determining organ polarity . A critical stage of fruit patterning occurs at fertilization which, when successful, results in seed formation. Fruit of most species will abort if there is none or limited fertilization and seed set. Phytohormones, particularly auxin and gibberellins (GA), play critical roles in fruit set and early growth triggered by pollination and fertilization. Auxin and GA can also induce parthenocarpic fruits by triggering pollination-independent fruit growth in several species including tomato [11–15].
Descriptions of flower and fruit developmental stages have been established for several species. The stages have been used to interpret gene function, and to determine the spatial and temporal expression of genes involved in organ identity and patterning. In addition, detailed descriptions of developmental stages are needed for comparative analyses to unravel genetic and molecular mechanisms that give rise to floral and fruit diversity. Ideally, these stages should describe key developmental events that are shared among flowering plant species, so that the landmarks could be compared and queried across databases using key morphological developmental features. Buzgo et al (2004) compared three distant angiosperm species and proposed ten floral landmark stages. These landmarks comprise "inflorescence formation and flower initiation", "sepal initiation", "petal initiation", "stamen initiation", "carpel initiation", "microsporangia formation", "ovule initiation", "male meiosis", "female meiosis", and "anthesis" , which have been adopted in studies of several other species [17, 18]. However, key fruit landmark stages that are applicable across species have not been described to date. For example, whereas Arabidopsis fruit development is described in eight stages, tomato fruit development is described in four [19, 20]. Phase I of tomato fruit development comprises ovary development ending with fertilization. Phase II describes early fruit growth following fertilization and spans cell division and early embryo development. Phase III spans cell expansion and embryo maturation. The final phase IV is the ripening phase . Both cell division and elongation occur concomitantly in the different parts of the tomato fruit, thus these two phases are not well separated during growth of the organ [21, 22]. More importantly, the stages described for Arabidopsis and tomato detail species-specific events that are not applicable across species. Therefore, the establishment of universally applied fruit developmental landmarks would allow comparative analysis of data obtained from different species.
Tomato, classified as a berry fruit, represents an excellent model for floral and fruit development and is used extensively in comparative studies within the Solanaceae family [2, 3, 19, 23]. Whereas some information is known about the regulation of organ identity and specification [24–29], information about fruit patterning in Solanaceous species is rather limited. Varieties that differ in fruit morphology offer an important resource to further our understanding on its patterning. Fruit size and shape of tomato are controlled by major and minor QTL loci [2, 3, 30]. For some of these major QTL, the underlying genes are known. SUN and OVATE control fruit elongation and therefore affect patterning along the apical-basal axis [31, 32]. FW2.2 and FAS control fruit mass via increases of the placenta area and locule number, respectively, and thus affect patterning along the medio-lateral axis [33, 34]. SUN encodes a member of the IQD protein family . The founding member of the IQD protein family AtIQD1 is localized in the nucleus and its overexpression leads to increases in glucosinolate production in Arabidopsis . The high expression of SUN in tomato leads to elongated fruit, whichis hypothesized to control increases in secondary metabolites and/or hormone levels. In the near-isogenic lines (NILs) that differ at SUN, the most significant fruit shape changes occur after anthesis during fruit set . However a detailed developmental time-course describing fruit shape changes that would aid in understanding the mechanism by which SUN acts has not been described. Moreover, an evaluation of flower and fruit expression profiles in the S. pimpinellifolium LA1589 background has not been performed to date.
In this study, we adopt the floral landmarks established previously , and also propose new landmarks of fruit development that are applicable across angiosperm plant species. These landmarks are superimposed onto the fruit shape changes controlled by SUN and combined with gene expression profiles of floral buds 10 days prior to anthesis, anthesis-stage flowers and fruit 5 days post pollination.
We used S. pimpinellifolium accession LA1589 for the tomato flower and fruit developmental studies due to its indeterminate growth habit and the abundant number of flowers and inflorescences throughout its life cycle. For example, LA1589 carries on average 20 flowers per inflorescence (Fig. 1A and 1B), whereas a typical cultivated variety carries only 3 to 7 flowers per inflorescence . In addition, flower development is highly regular in the wild relative LA1589 compared to most cultivated types . To time the developmental stages of consecutive buds and then fruits on an inflorescence, we recorded the time of anthesis for each flower in a total of 83 inflorescences investigated over four independent experiments. As shown in Figure 1C, the second flower opened 70% of the time one day after the first flower, 29% of the time on the same day as the first flower, and 1% of the time two days after the first flower and so on. In general, consecutive flower opening occurred at one-day intervals 75% of the time, until the 16th flower on a given inflorescence (Fig. 1C). Flower buds developed after the 16th on a given inflorescence tended to open more irregularly and often at an interval of 2-days or more. By inference, this result implied that the first 16 floral meristems arose 75% of the time in one-day interval from one another. Therefore, we concluded that until the 16th flower on a given inflorescence, the developing flower and fruit respectively, are staged at close to one-day intervals from one another.
Initiation of floral organ primordia
The first landmark represented inflorescence formation and flower initiation (Table 1). The transition to flowering and inflorescence formation in LA1589 has been described previously . Briefly, transition to flowering commenced with the termination of the vegetative meristem into an inflorescence meristem. Floral initiation occurred through the apparent bifurcation of the inflorescence meristem resulting in bud number 1 (Fig. 2A and 2B). The flatter inflorescence meristem continued its indeterminate growth pattern, while the more domed meristem developed into a flower (Fig. 2A and 2B). Following flower initiation, the emergence of the sepal primordia around the perimeter of the floral apex of bud number 2 marked the second landmark (Fig. 2A). The five tomato sepals initiated in a helical pattern of 144° (Fig. 2C). The sepals continued to grow and covered the floral meristem approximately 4 days after floral initiation (Fig. 2D and 2E). At the time of sepal enclosure, petal primordia started to arise, representing landmark 3. Following petal primordia emergence, stamen primordia emerged in alternate positions to the petals (Fig. 2F and 2G), at approximately 5 days after floral initiation, representing landmark 4. Sepals and petals continued to elongate while carpel primordia began to emerge in the floral center (Fig. 2G), marking landmark 5, which occurred approximately 6 days after floral bud initiation. The carpel walls or valves continued to enlarge, while the central part comprising the septum and the central column formed congenitally with the carpel walls, revealing the formation of the two locular cavities of wild type tomato ovary (Fig. 2H). The carpel walls elongated slightly faster than the central column revealing the locular cavity prior to ovary enclosure and initiation of the style, which occurred 8 days post bud initiation (Fig. 2I and 2J).
Reproductive organ formation
Male reproductive development initiated with microsporangia development, which represented landmark 6, and occurred approximately eight days after floral bud initiation (Table 1 and Fig. 3A). The primary sporogenous layers were visible at this stage (Fig. 3A). Nine days after floral bud formation, the tapetal cells were binucleate, and the developing microsporocytes were also visible (Fig. 3B and 3C). At 10 days after floral bud initiation, microsporocytes or pollen mother cells were undergoing meiosis (Fig. 3D), marking landmark 8. A callose wall surrounded the four haploid nuclei of the tetrads (Fig. 3E). One day later, the callose walls began to degrade and the microspores were being released (Fig. 3F). At 13 days after floral bud initiation, the tapetum was degenerating; and the microspores were single and encapsulated in a thick wall (Fig. 3G and 3H). One day later, the microspores became vacuolated (Fig. 3I) and underwent one asymmetric mitosis. Fifteen days after floral bud initiation, the microspores were bi-cellular (Fig. 3J) and a day later, the generative and vegetative cells were clearly distinguishable within the developing pollen (Fig. 3K). At day 17 after floral bud initiation, the generative cell displayed the characteristic crescent shaped nucleus (Fig. 3L and 3M). The second mitosis of the generative cell did not occur until after pollination.
Female reproductive development initiated with the development of the ovules and represented landmark 7 (Fig. 4A). Approximately 9 days after floral bud initiation, the style and the ovary were nearly equal in length, and ovule primordia were emerging on the placental tissues (Fig. 4A). Ovules were clearly visible one day later (Fig. 4B). Two days after ovule primordia initiation and 11 days after floral bud initiation, a single integument started to envelope the single cell layered nucellus and the developing megasporocyte, resulting in a unitegmic tenui-nucleate ovule representing landmark 9 (Fig. 4C). Apparently the megasporocyte underwent the first meiotic division at this stage (Fig. 4D). A day later, the single integument at the base of the nucellus was clearly visible, while the megasporocyte is undergoing the second meiotic division, representing the first stage of megagametogenesis (Fig. 4E). Fourteen days after floral bud initiation, the integument enveloped the nucellus completely and the micropyle was well defined. The embryo sac development was taking place as evidenced by concentrated dark staining at the micropyle end. The presence of the megaspore at the chalaza end of the ovule indicated the development of the egg apparatus (Fig. 4F).
Fertilization and fruit set
Anthesis or flower opening was the final floral landmark as well as the first fruit landmark (Table 1 and 2). At the time of anthesis, the anther lobes dehisced to release the pollen, which after landing on the receptive stigma, germinated. Pollen tubes had grown close to the base of the style 6 hours after pollination, and reached the ovules approximately 2 hours later (Fig. 5A and 5B). Ten to 12 hours after pollination, the pollen tubes had released their content resulting in fertilization of the ovules (Fig. 5C) and representing fruit development landmark 2 (Table 2). Senescence of floral organs, namely petal, stamens and style is associated with successful fertilization and was visible approximately two days after anthesis as shown in Fig. 1B.
Development of the pericarp after pollination
Following fertilization, tomato fruit growth consists of cell division and cell expansion . We analyzed the growth of the pericarp following pollination to establish the timing of cell division and cell elongation in the developing LA1589 pericarp. Pericarp width doubled from anthesis to 2 days post anthesis (dpa), and then further doubled at 5 and 10 dpa, respectively (Fig. 6). Cell number across the pericarp increased from 10 at anthesis to 17 at 2 dpa, and reached the final number of 19–21 at 5 dpa (Fig. 6F), implying that cell division ended at or before that time. Mesocarp cell expansion started as early as 2 dpa (Fig. 6B). These results indicated that cell division and expansion occurred concurrently in the pericarp of the early developing fruit. Note the presence of the cuticle layer and starch granules in the epicarp and mesocarp respectively, of 10 dpa fruit (Fig. 6D).
As indicated above, cell division overlapped with cell elongation during the early stages of fruit development. Moreover, the cell division stage was short, ending before 5 dpa in LA1589, whereas the cell elongation stage spanned fruit development from 2 dpa until mature green stage. Thus, these two fruit developmental stages, which correspond to tomato development phases II and III, provided limited guides for referencing. To develop additional landmarks for the developmental stages of tomato fruit growth, we analyzed morphological changes in embryo development, which occur concomitantly with fruit growth in most angiosperm plant species.
We propose the third fruit developmental landmark as the stage of 4–16 celled embryo, which occurred approximately 4 dpa (Fig. 7A and 7B). The fourth landmark was represented by the globular embryo stage at 6 to 10 dpa (Fig. 7C and 7D). Heart shape embryo was the fifth landmark and occurred between 10 and 12 dpa (Fig. 7E and 7F) highlighting the beginning of cotyledon growth. The 13–16 dpa embryo was torpedo shape, marking the sixth landmark (Fig. 7G and 7H). After the sixth landmark, the cotyledons grew into a coil and reached the seventh landmark approximately at 20 dpa. At this stage, the embryo approached its final size, but the seed was not yet viable for germination (Fig. 7I and 7J). The eighth fruit developmental landmark was reached when the seeds harvested from the maturing fruit were viable for germination. Seed were collected from maturing fruit starting at 26 dpa until 33 dpa. Up until 29 dpa, there was little or no seed germination (Fig. 8). However, at 30 dpa, the germination rate increased dramatically thus reaching landmark eight. At 32 dpa, nearly 100% of the seeds germinated.
Tomato fruit ripening stages consist of mature green, breaker and red ripe [19, 23]. At the mature green stage, ethylene treatment will result in a rapid reddening of the fruit [23, 37–39]. We measured ethylene sensitivity in half of the harvested fruits while determining the germination ability of the seed in the other half that were collected at selected times (see above). Ethylene sensitivity was achieved over a short period of up to two days, and coincided with the time when the seed became viable for germination (Fig. 8). Forty percent of fruit had responded to ethylene at 30 dpa when 43% of the seeds were viable for germination. Fruit younger than 29 dpa did not respond to ethylene treatment (Fig. 8). The ninth landmark is the onset of fruit ripening, coinciding with the breaker stage when color began to change at approximately 32 dpa. This stage is followed by the tenth and final landmark of ripe fruit.
Gene expression profiles of floral and fruit development
To obtain a global overview of gene expression in flower and fruit, we compared the profiles between three critical developmental time points. The first stage was young flower buds at floral landmark 7, representing ovule initiation (10 days pre-anthesis). The second stage was the anthesis-stage, representing flower landmark 10 and fruit landmark 1. The third and last stage was 5 dpa fruits, representing the 4–16 cell embryo stage and fruit landmark 3. Differentially expressed genes were identified using the resampling-based multiple testing method . Without the cutoff of fold-change applied, 2495 genes with adjusted p < 0.01 were differentially expressed in at least one of the three stages (see Additional file 1). Among them, 1232 genes showed higher expression at anthesis, whereas 527 and 736 genes showed higher expression in young flower buds and 5 dpa fruits, respectively (Table 3). Functional classification of the differentially expressed genes showed a distinct distribution of genes involved in various biological processes for the three stages investigated. For example, more genes involved in developmental processes were found in flower buds during ovule initiation and anthesis-stage flowers than in 5 dpa fruit. On the other hand, phytohormone-related genes were predominantly found in anthesis-stage flowers and 5 dpa fruits compared to flower buds (Table 3).
Expression of organ identity and patterning genes
Of the genes representing the developmental processes, key floral and fruit patterning genes were examined for their expression profiles during reproductive development (see Additional file 2, Fig. 9). Genes orthologous or homologous to the Arabidopsis ABCE genes required for floral organ identity have been identified in tomato [41, 42]. On our array, the tomato floral organ identity genes differentially expressed at the three stages include B class genes TAP3 (TC116723) , TPI (TC117703) and SlMBP1/LePI-B (TC119919) , C class gene TAG1 (TC124766) , and E class gene TM29 . The tomato ortholog TC121763 of Arabidopsis NAP that is directly activated by B class gene APETALA3 and PISTILLATA in Arabidopsis  was also differentially expressed. All the above-mentioned genes showed higher expression in floral buds and/or anthesis-stage flowers (see Additional file 2), in agreement with their previously identified expression patterns. Another tomato B class gene TM6 (TC117238) was not differentially expressed, likely due to its more ubiquitous expression in floral organs . While there is no clear ortholog of Arabidopsis A class genes in tomato , the closest related AP1 gene, MADS-MC (TC118643) , showed no expression changes in the three developmental stages. Many of the organ identity genes encode MADS box proteins of MIKC-type, and in vitro interaction analysis of twenty-two tomato MADS box proteins show modified as well as novel interaction patterns that had evolved for the family members in this species .
In addition to these organ identity genes, other genes play key roles in patterning of the fruit. In Arabidopsis, these include the apical-basal patterning genes: ETTIN (ETT) , LEUNIG (LUG) , TOUSLED (TSL) , STYLISH (STY1 and STY2) , SPATULA (SPT) , NO TRANSMITTING TRACT (NTT) , and HECATE (HEC1, HEC2 and HEC3) , involved in basal valve growth, carpel and septum fusion, elongation of apical tissues, and style and transmitting tract formation, respectively. There are also genes patterning valve and valve margin of the fruit along the medio-lateral axis, including SHATTERPROOF (SHP) , ALCATRAZ (ALC) , INDEHISCENCE (IND) , REPLUMLESS (RPL) , and FRUITFULL (FUL) . The Arabidopsis gene SEEDSTICK (STK) is required for ovule identity and patterning as well as seed disposal , and ERECTA (ER) regulates fruit shape by controlling cell expansion and cell division . JAGGED (JAG) acts redundantly with the polarity genes FILAMOUS FLOWER (FIL) and YABBY3 (YAB3) to activate FUL and SHP . Additional polarity genes required for proper patterning and establishment of organ boundaries are CRABS CLAW (CRC) , KANADI (KAN1 and KAN2) , GYMNOS (GYM) , PHAVOLUTA (PHV) and PHABULOSA (PHB) . Tomato genes homologous to Arabidopsis patterning genes FIL (TC126122), FUL (TC125305 and TC126125), CRC (TC125410), ER (TC121018, TC122809 and TC123029), PHB (TC130887), and SPT (TC126307) were more abundantly expressed in tomato flower buds compared to the other tissues. The tomato SHP homolog TC118705 showed higher expression in anthesis-stage flowers and fruits at 5 dpa than in floral buds. The STK homolog in tomato TAGL11 (TC119398), which is expressed in the inner integument of the ovules and the endothelium in developing seeds , was expressed higher in fruits at 5 dpa compared to other time points (see Additional file 2), suggesting that it may also play a role in tomato fruit development. Tomato genes with high similarity to Arabidopsis fruit patterning genes ETT, GYM, KAN2, LUG, PHV, RPL, HEC1, STY1 and TSL were not differentially expressed between the three stages, whereas no tomato homologs for JAG, NTT, ALC, IND, YAB3, STY2 were included on our array. Further, the hierarchical clustering of all the 122 differentially expressed developmental processes genes revealed that flower bud and 5 dpa fruit shared expression profiles of the same developmental genes, whereas anthesis-stage flower showed a distinctive profile (Fig. 9, see Additional file 2), which is in agreement with results from other gene profiling studies in Arabidopsis [66–68].
Expression of phytohormone-related genes
Phytohormones play essential roles in many aspects of plant development. Among the three developmental time points, 79 phytohormone-related genes were differentially expressed (see Additional file 3). Of these genes, 30 were involved in auxin conjugation, transport or signaling. Most of the auxin-related genes (22 of 30) were either up- or down-regulated in 5 dpa fruit (Fig. 10, see Additional file 3). Moreover, most of the genes with similarity to GH3 involved in IAA conjugation were repressed after pollination, whereas three auxin response factor genes TC118569 (ARF4), TC122720 (ARF8), and TC122700 (ARF9), were expressed at the lowest level in anthesis stage flowers. Further, transcripts of three auxin transporter genes, TC127164, TC123055 and TC120936, homologous to AUX1, PIN4 and an auxin efflux carrier family protein, respectively, were less abundant in 5 dpa fruit (Fig. 10, see Additional file 3). Several genes involved in biosynthesis of tryptophan (TC119571, TC121695, TC125473, TC127841, TC129375, and TC130235), a precursor of IAA, were not developmentally regulated in this study, neither was the ortholog of Arabidopsis auxin receptor TRANSPORT INHIBITOR RESPONSE1 (TIR1, TC121284) . The ortholog of ALDEHYDE OXIDASE 1 (AAO1, TC117167) involved in auxin biosynthesis , was expressed at higher level in anthesis flower. This may imply that many components in auxin pathway are channeled to the increasing demand for auxin-dependent programs to fulfill rapid fruit growth after pollination.
Some GA-related genes were also differentially expressed in the three developmental stages. Transcript levels of the tomato ortholog TC124105 of AtKAO2 that catalyzes the conversion of ent-kaurenoic acid to GA12 in gibberellin biosynthesis pathway , was more abundant in 5 dpa fruit compared to other stages. In contrast, the expression of SlGA2ox2 (TC127124), involved in catabolism of GA , was lower in the developing fruits than in flower buds at 10 days preanthesis and anthesis-stage flowers. Interestingly, transcripts of three tomato homologs TC118018, TC121133 and TC124715 of Arabidopsis GA receptors GA INSENTIVE DWARF1B and C (GID1B and GID1C) , were less abundant in 5 dpa fruit. This suggests that although GA levels may increase in 5 dpa fruit as a result of increased biosynthesis and reduced catabolism, the sensitivity to the hormone may decrease as a result of reduced expression of the receptor. GA biosynthesis genes of the GA 20-oxidase and GA 3-oxidase families were either not differentially expressed (SlGA20ox-3, SlGA3ox-2) or not included on the array (SlGA20ox-1, -2 and SlGA3ox-1, -3). Most of the seven GA responsive genes were not differentially expressed following pollination with the exception of tomato gene TC126562 encoding GASA/GAST/Snakin family protein that was upregulated after anthesis (Fig. 10, see Additional file 3).
Transcripts of all the eight brassinosteroid-related genes were more abundant in 5 dpa fruit, whereas the majority of jasmonate- and ethylene-related genes were less abundant in 5 dpa fruit (see Additional file 3). Expression of genes involved in ABA biosynthesis and response like were also lower in 5 dpa fruits. The putative ortholog of Arabidopsis gene CYP707A3 (TC129465), encoding the major ABA 8'-hydroxylase involved in ABA catabolism , is expressed at higher level in 5 dpa fruit compared to the other stages, suggesting that the ABA levels are reduced during the early fruit growth.
Fruit shape changes in LA1589 NILs differing at sun
We used the floral and fruit developmental landmarks described above to determine when SUN affects tomato fruit shape. SUN controls fruit elongation and its high expression results in oval shaped fruit . We analyzed the changes in fruit shape from anthesis onward in NILs in LA1589 background differing at the sun locus because at anthesis the ovary shape is only marginally different (Fig. 11). The LA1589pp has round fruit and carries the wild type allele, while LA1589ee carries the Sun1642 allele of sun resulting in an elongated fruit (Fig. 11A). The difference in fruit shape between the two NILs became apparent immediately following fertilization and was most pronounced between 6 and 10 dpa coinciding with the globular embryo stage of fruit landmark 4. At the end of the sixth fruit landmark, representing the seed torpedo stage, the fruit shape index of the LA1589ee NIL started to decrease. After the landmark of seed germination corresponding to mature green stage, the fruit shape index remained constant. LA1589pp fruit showed a decrease in fruit shape index from > 1 at anthesis to < 1 at 5 dpa (Fig. 11A). We examined SUN expression in the developing fruits of the LA1589 NILs starting from anthesis-stage ovaries until ripe fruit. In LA1589ee, SUN was expressed at a high level until fruit landmark 7 coinciding with coiled embryo and seed maturation stage at 20 dpa (Fig. 11B). A detailed investigation of its expression immediately before and after anthesis showed that SUN transcript levels increased from 2 days prior to anthesis to 2 dpa and thus showed a similar kinetics to that of the changes in fruit shape (Fig. 11B).
Gene expression profiles associated with SUN
To further investigate the effect of SUN on tomato fruit shape and to identify genes that may interact with SUN in regulating morphology, we compared transcriptional profiles of three floral and fruit developmental stages in the NILs in LA1589 background that differ at sun. The stages selected represented the three important events in flower and early fruit development when SUN exhibited the greatest differential gene expression (Fig. 11B), namely 10 days pre-anthesis, anthesis and 5 days post-anthesis fruit. In total, we found 34 differentially expressed genes between the NIL pairs (p < 0.05 and fold change FC > 1.4) (see Additional file 4, Table 4). One of the genes, DEFL2 encoding a member of plant defensins, was differentially expressed at all three time points. Another gene encoding maternal effect embryo arrest 59 (MEE59, TC125885) was upregulated in oval shaped fruit at two time points. Twenty four genes were differentially expressed only in anthesis-stage flowers and eight genes were differentially expressed only in 5 dpa fruit. The differences in the transcript levels of the 34 genes were less than two-fold with the exception of DEFL2. The latter gene is located very close to SUN on chromosome 7. Therefore, decreased DEFL2 expression in the NIL carrying elongated fruit was likely due to the mutation at the locus and not a consequence of increased expression of SUN (see sequence annotation EF094940). The remaining differentially expressed genes did not fall into known developmental pathways. Note that SUN and DEFL1, which are differentially expressed in these NILs  were not on the array.
SUN has been hypothesized to affect fruit shape by altering hormone levels such as auxin . However, several auxin biosynthesis genes, including ALDEHYDE OXIDASE 1 (AAO1) and most genes encoding tryptophan biosynthesis enzymes that were present on the array, were not changed in the NILs. Gibberellins (GA) also play important roles in cell division and elongation [75, 76]. Similarly, none of the GA biosynthesis genes on the array were differentially expressed. We also performed Northern blots on GA biosynthesis genes that were not on the array and found that none were differentially expressed in the NILs either (data not shown). This implied that SUN is not directly involved in regulating auxin and GA levels.
The formation of the flower and fruit can be described by a series of landmarks that coincide with key development events. Floral landmarks described by Buzgo et al. (2004) and fruit landmarks proposed herein provide the framework for comparative analyses of floral and fruit development among angiosperm species. Moreover, understanding the common mechanisms of reproductive development also provides the basis from which to dissect the differences observed among species and the evolution of fruit form .
For tomato, S. pimpinellifolium accession LA1589 is an excellent model for flower and fruit development because of its predictable growth pattern, large numbers of flowers per inflorescence and inflorescences per plant. Previous studies in cherry tomato (S. lycopersicum var. cerasiforme) described flower development in 20 stages from sepal initiation to anthesis and established the correlation between major cellular events in reproductive organs with perianth markers . The main floral developmental events we described for LA1589 are in agreement with those observations in cherry tomato, although we started floral development with inflorescence formation and floral initiation rather than sepal initiation. Inflorescence formation and floral initiation is a major event in floral development, and the critical transformation from vegetative meristem to floral meristem is tightly regulated by floral meristem identity genes, such as LEAFY and APETALA1 [79, 80]. Therefore, floral landmark 1 will be of great interest in dissecting functions and expression patterns of floral meristem identity genes in tomato as well as genes that play a role in fruit size and shape. Previous fruit development of cultivated tomato has been divided into phases based on cell division activities . We observed a very short duration of cell division in the pericarp of LA1589 fruit (less than 5 dpa), in contrast to ~7 to 10 dpa in cultivated tomato . Embryogenesis and seed formation in many flowering plants occur concomitantly with fruit development, therefore we described the ontogeny of the fruit following key events in embryogenesis and seed formation. Thus, herein we provide a complete set of consensus landmarks for flower and fruit stages starting from floral initiation until fruit ripening. These landmarks highlight major events in reproductive development and serve as a guide in floral and fruit developmental research. The use of common terminology will make data and information from different species queryable, while also facilitates comparative analysis across species.
Recently, a genome-wide analysis of the transcriptional changes induced by pollination and GA application of ovaries was performed . A comparison between ours and the previously published study showed that some phytohormone related genes were shared in the two studies. Four auxin-related genes, encoding GH3.3 (TC118161), auxin responsive family protein (TC130798), amino acid permease (TC122973) and auxin efflux carrier family protein (TC120936), shared the same expression patterns between the two experiments. However, none of the GA-related genes were shared in the two studies. Abscisic acid (ABA) and ethylene may also play roles in fruit set and fruit growth post pollination as genes involved in biosynthesis and signaling of these phytohormones were differentially expressed after pollination . Similar to the Vriezen et al study (2008), several ACC synthase genes were differentially expressed and all the ethylene biosynthesis genes were less abundant in 5 dpa fruits, suggesting reduced levels of this hormone after pollination. The expression of ABA biosynthesis genes, such as neoxantin synthase (NSY) and 9-cis-epoxycarotenoid dioxygenase (LeNCED), is reduced in fruits post pollination . Similarly, in our study zeaxanthin epoxidase (ZEP/ABA1) was less abundant in 5 dpa fruit compared to flower. In both studies, an ABA 8'-hydroxylase gene (cytochrome P450 family member) involved in ABA catabolism , was more abundant in fruits post pollination. This suggests that ABA, like ethylene, is in low demand during fruit set and early growth. Recently, Galpaz et al (2008) determined that tomato high-pigment 3 (hp3) mutant with a mutation in the ZEP gene produces a higher level of fruit lycopene linked to increased plastid number as a result of ABA deficiency . Because the hp3 mutant makes smaller fruit , certain amounts of ABA may be required for fruit growth after anthesis.
Transcriptional profiles of other classes of genes were also similar between the previously published study  and ours. More than half (13 of 22) of cell cycle-related genes and half (13) of the cell wall-related genes were shared between the two studies (see Additional file 5) . Two cyclin genes TC120949 and TC128804, showing highest similarities to Arabidopsis CYCLIN D3;1 (CYCD3;1) and CYCLIN B1;4 (CYCB1;4), were induced by pollination, but not by GA treatment based on previous observations . However, their higher expression before and after anthesis in our experiments suggests that the two genes are not only inducible by pollination but also involved in pre-anthesis activation of cell division possibly in response to other hormone cues such as cytokinin. In Arabidopsis, CYCD3;1 responds to cytokinin to activate cell division at the G1-S cell cycle phase .
After establishing the morphological landmarks for flower and fruit development in tomato, we superimposed the effect of SUN on fruit formation. SUN controls fruit shape after anthesis . From the landmark fertilization to the landmark globular embryo stage, the fruit shape index dramatically increased in the accession that expresses SUN to a high level (Fig. 11). The coincidence between the dynamics of fruit shape index mediated by SUN and fruit growth suggests that SUN mainly acts in fast growing tissues, which is further supported by high expression of SUN in the oval shaped fruits during early fruit growth. Although we hypothesized that SUN may indirectly affect hormone or secondary metabolite levels and as such altering organ shape , the identified differentially expressed genes did not support that notion. Moreover, the very low number of differentially expressed genes was surprising considering that the expression of SUN was quite high in the lines carrying oval-shaped fruit at the time points sampled.
Following the universal landmarks proposed by Buzgo et al (2004), we outlined flower and fruit developmental landmarks in tomato. Transcriptional profiles of flower and developing fruit at three main stages have been integrated with their corresponding landmarks, which will be useful for identifying important regulatory components responsible for key developmental processes. We identified genes encoding patterning, phytohormone and cell cycle-related proteins modulated during flower and early fruit development, which will provide basis for further studies on tomato fruit growth. The usefulness of the landmarks was demonstrated by examining the fruit shape changes mediated by SUN.
Seeds of S. pimpinellifolium accession LA1589 were obtained from the C.M. Rick Tomato Genetics Resource Center, Davis, California, USA. Nearly Isogenic Lines (NILs) that differ at sun locus were resulted from the high-resolution recombinant screens conducted to fine map the locus . After multiple backcrosses and molecular marker analysis, we estimated that the introgression of the Sun1642 allele in the LA1589 background is less then 100 kb with very few, if any, other regions of the genome harboring the Sun1642 allele. Plants were grown under standard conditions with supplemental lighting in the greenhouse.
Timing of flower opening on individual inflorescences
Eighty three inflorescences from four independent experiments were tagged before flower opening. Anthesis was recorded each day at the same time, and two flowers that opened on the same day were recorded as 0 days between flowerings.
Seed viability determination
Seeds were extracted from the fruit harvested on tagged inflorescences that were hand pollinated to ensure uniform fruit set. The dates of pollination were recorded and the fruits were harvested based on days after anthesis. Seeds were extracted and incubated for 20 min in 25% HCl to remove the gelatinous layer surrounding the seed, rinsed with distilled water and germinated for one week in the dark at 30°C on moist Whatman paper.
Ethylene sensitivity of developing fruit
Tagged flowers were hand pollinated and the dates were recorded. Fifteen to 20 fruit from mature green to breaker (26–33 dpa) were treated for 16 hours in a sealed chamber with 10 μl/L ethylene and the color changes were monitored two days later. Color for each fruit was recorded into different categories (green, color turning, orange, yellow and red) before and after ethylene treatment, and ethylene sensitivity was expressed by fruits with changed colors in total fruits assayed.
Timing of fertilization
Flowers were emasculated one day prior to anthesis and hand-pollinated the next day. Pistils were collected at 6, 8, 10, 12 and 24 hours after pollination. Dissected pistils were fixed in 3:1 95% ethanol:glacial acetic acid overnight at room temperature. Samples were subsequently softened for 24 hours in 10 N NaOH, rinsed five times in ddH2O and stained using 0.1% aniline blue (aniline blue fluorochrome, Biosupplies Australia) in 0.1 M potassium phosphate buffer pH8.0 for 4 hours in the dark. Samples were mounted in 30% glycerol and viewed on a Leica DM IRB epifluorescence microscope using the UV filter set (Chroma filter A, BP340-380, LP425).
Fruit shape changes during development
Data were collected from five individual NIL plants per genotype homozygous for sun. For ovary and developing fruits from anthesis to 34 dpa, developing fruit were cut in half longitudinally and images were obtained using camera connected to dissection microscope (0–7 dpa) or using scanner (fruit older than 7 dpa). Shape index (length divided by width) were obtained with ImageJ http://rsb.info.nih.gov/ij/ on images taken. Each time point has at least three ovaries or fruits from each individual plant.
Scanning electron microscopy of floral development
Flowers were processed in its entirety or partially dissected under the dissecting microscope prior to fixation. Samples were infiltrated and fixed with 3% gluteraldehyde, 2% paraformaldehyde in 0.1 M potassium phosphate buffer pH7.4 for two hours at room temperature and then over night at 4°C. After 3 washes with ddH2O samples were post fixed with 1% osmium tetroxide, washed 3 times with ddH2O and dehydrated following a graded ethanol series (once for 25%, 50%, 70%, 90%, twice 100%). Critically point dried (Samdri-790, Tousimis Research Corporation) samples were mounted on aluminum stubs, and sputter-coated with platinum (Polaron). When necessary, flower buds were further dissected after platinum coating. Samples were viewed and images recorded with a Hitachi 3500N scanning electron microscope under high vacuum.
Flower and fruit samples were infiltrated and fixed in 3% glutaraldehyde, 4% paraformaldehyde, 0.05% Triton X-100 in 0.1 M potassium phosphate buffer at pH 7.2 for two hours at room temperature and then over night at 4°C. After three washes with potassium phosphate buffer, samples were processed for embedding into London Resin White (LRW) (EMS) or paraffin (PolyFin, Polyscience).
For LRW embedding, samples were dehydrated in a graded ethanol series (25%, 50%, 70%, twice 90%), infiltrated with a graded resin and 90% ethanol series (1:3, 1:1, 3:1, twice 100% resin), embedded in airtight gelatine capsules (EMS) and polymerized overnight at 60°C. Five μm thick sections were collected on glass slides and stained with 0.1% sodium bicarbonate, 0.5% toluidine blue, in 25% EtOH before light microscopy observation.
For paraffin embedding, samples were dehydrated in a graded ethanol series (50%, 80%, 90% twice 100%), and subsequently infiltrated, first in a graded ethanol/tertiary butyl alcohol (TBA) series at room temperature (2:1, 1:1, 1:2, twice 100% TBA), and then in a graded TBA/paraffin series (1:3, 1:1, 3:1, twice 100% paraffin) at 56°C and embedded in paraffin. 6–10 μm sections were collected on silane treated glass slides (Polyscience). Deparaffinized sections were stained 10 minutes with 10 mg/ml safranin O in 50% ethanol, and 10 seconds with 5 mg/ml astra blue containing 20 mg/ml tartaric acid following Jensen procedure . Sections were observed on the Leica DM IRB light microscope (Leica Microsystems, Wetzlar Germany) and images were captured using the MagnaFire model S99802 digital camera (Optronics, Goleta, CA).
For fluorescent microscopy, sections were deparaffinized, blocked with 10 mM potassium phosphate buffer (pH7.4), 150 mM NaCl (PBS) containing 10 mM NaAzide, 0.2%BSA, 1% normal goat serum for 30 minutes. Tubulin was detected using a 1/500 dilution of the mouse anti-tubulin monoclonal IgG1 (Molecular Probes) as primary antibody, and AlexaFluor488 sheep anti-mouse secondary antibody (Invitrogen, USA). Antibody incubations were performed in incubation buffer (PBS containing 10 mM NaAzide, 0.2%BSA) at room temperature for 4 hours for the primary antibody, and 2 hours for the secondary antibody. After each incubation, the sections were washed five times with PBS. Cell nuclei were counterstained for 8 minutes with 0.25 mM SytoxOrange (Invitrogen, USA). Sections were then mounted with GelMount (Biomedia) and observed on a Leica TCS-NT confocal microscope.
Additional developing embryos were visualized using differential interference contrast microscopy. Samples were fixed in 10:3:1 ethanol, glacial acetic acid, chloroform mixture. Tissue was rinsed in 90% ethanol twice, and then cleared in modified Hoyer's solution consisting of 60 ml of distilled water, 7.5 g arabic gum, 100 g chloral hydrate, 5 ml of glycerin. Samples were mounted in 70% glycerol, smashed using the cover slip and viewed with a Nomarski objective or phase contrast using the Leica DM IRB light microscope.
Pericarp cell number and size measurements
Fruits were harvested at 0, 2, 5, and 10 dpa. Prior to fixation, fruit of 5 and 10 dpa were cut longitudinally and perpendicular to the septum, while fruit of 0 and 2 dpa were fixed as a whole. The fixed tissues were embedded into London Resin White as described above. Sections were collected from 6 and 20 samples per time point. Pericarp consists of epicarp (the single outermost cell layer), endocarp (the single innermost cell layer) and mesocarp comprising of cells in-between epicarp and endocarp. Cell lengths of epicarp and endocarp were determined by averaged lengths of 5–10 cells along. The length of the mesocarp was measured in the middle region of the mesocarp sampling 5–10 cells. Cell volume was calculated based on formula V = L*W*((L+W)/2), where V represents cell volume, L = cell length, W = cell width.
The tomato microarray was custom-designed oligoarray manufactured by Nimblegen (Nimblegen Inc. USA) based on TIGR tomato Tentative Contigs sequences (release 9, http://compbio.dfci.harvard.edu/tgi/cgi-bin/tgi/gimain.pl?gudb=tomato). It consists of 15270 TCs corresponding to 7600 different clusters (transcripts) and each TC was represented by 12 pairs of perfect and mismatch probes of 24-mers.
Total RNA for microarray analysis were extracted from 10-day preanthesis flower bud and anthesis flower and fruits at 5 dpa using Trizol reagent (Invitrogen Inc. USA). Before RNA extraction, tissues harvested at 7-day interval from five plants were pooled for each genotype. Three biological replicates were conducted with three sets of LA1589 sun NILs growing during different time periods resulting in 3 time points × 2 genotypes × 3 replicates = 18 array hybridizations. Microarray hybridizations, image scanning and data extracting were performed by Nimblegen Inc. Background correction and data normalization were performed by Robust Microarray Analysis (RMA, ) in Bioconductor. Differentially expressed genes (DEs) among the three stages were selected by multiple testing package multtest  of R http://www.r-project.org using the RMA expression values. To update the gene description and annotation, sequences of the differentially expressed genes were BLASTed against Arabidopsis protein database (version 7 released on July 24, 2007 by TAIR, http://www.arabidopsis.org.) using blastx. Description of proteins encoded by some differentially expressed genes with low homology (p < 1e-10) to Arabidopsis proteins was assigned with the annotation of the newest TC (release version 11 by TIGR) or those with best hit in NCBI database http://www.ncbi.nlm.nih.gov. The data discussed in this publication have been deposited in NCBI's Gene Expression Omnibus  and are accessible through GEO Series accession number GSE15453 http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/geo/query/acc.cgi?acc=GSE15453.
RNA was isolated from the whole fruit or flower using Trizol reagent (Invitrogen Inc. USA) (for ovary and fruits of 20 dpa or younger), or the hot borate method (for fruits of 25, 30, and 34 dpa old) . For Northern blot, 10 μg of the total RNA of each sample was separated in 1.2% Agarose gel in 1XMOPS buffer with formaldehyde, transferred onto Hybond N membrane (Amersham Biosciences) and hybridized at 42°C in formamide-containing hybridization buffer with radiolabeled gene-specific probes sequentially after previous probes were stripped.
Knapp S: Tobacco to tomatoes: a phylogenetic perspective on fruit diversity in the Solanaceae. J Exp Bot. 2002, 53: 2001-2022. 10.1093/jxb/erf068.
Paran I, Knaap van der E: Genetic and molecular regulation of fruit and plant domestication traits in tomato and pepper. J Exp Bot. 2007, 58: 3841-3852. 10.1093/jxb/erm257.
Tanksley SD: The genetic, developmental, and molecular bases of fruit size and shape variation in tomato. Plant Cell. 2004, 16 (Suppl): S181-189. 10.1105/tpc.018119.
Coen ES, Meyerowitz EM: The war of the whorls: genetic interactions controlling flower development. Nature. 1991, 353: 31-37. 10.1038/353031a0.
Ditta G, Pinyopich A, Robles P, Pelaz S, Yanofsky MF: The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity. Curr Biol. 2004, 14: 1935-1940. 10.1016/j.cub.2004.10.028.
Pelaz S, Ditta GS, Baumann E, Wisman E, Yanofsky MF: B and C floral organ identity functions require SEPALLATA MADS-box genes. Nature. 2000, 405: 200-203. 10.1038/35012103.
Theissen G, Saedler H: Plant biology. Floral quartets. Nature. 2001, 409: 469-471. 10.1038/35054172.
Balanza V, Navarrete M, Trigueros M, Ferrandiz C: Patterning the female side of Arabidopsis: the importance of hormones. J Exp Bot. 2006, 57: 3457-3469. 10.1093/jxb/erl188.
Dinneny JR, Yanofsky MF: Drawing lines and borders: how the dehiscent fruit of Arabidopsis is patterned. Bioessays. 2005, 27 (1): 42-49. 10.1002/bies.20165.
Dinneny JR, Weigel D, Yanofsky MF: A genetic framework for fruit patterning in Arabidopsis thaliana. Development. 2005, 132: 4687-4696. 10.1242/dev.02062.
Fos M, Proano K, Nuez F, Garcia-Martinez JL: Role of gibberellins in parthenocarpic fruit development induced by the genetic system pat-3/pat-4 in tomato. Physiol Plant. 2001, 111: 545-550. 10.1034/j.1399-3054.2001.1110416.x.
Gorguet B, van Heusden AW, Lindhout P: Parthenocarpic fruit development in tomato. Plant Biol (Stuttg). 2005, 7: 131-139. 10.1055/s-2005-837494.
Olimpieri I, Siligato F, Caccia R, Mariotti L, Ceccarelli N, Soressi GP, Mazzucato A: Tomato fruit set driven by pollination or by the parthenocarpic fruit allele are mediated by transcriptionally regulated gibberellin biosynthesis. Planta. 2007, 226: 877-888. 10.1007/s00425-007-0533-z.
Serrani JC, Ruiz-Rivero O, Fos M, García-Martínez JL: Auxin-induced fruit-set in tomato is mediated in part by gibberellins. Plant J. 2008, 56: 922-934. 10.1111/j.1365-313X.2008.03654.x.
Vivian-Smith A, Koltunow AM: Genetic analysis of growth-regulator-induced parthenocarpy in Arabidopsis. Plant Physiol. 1999, 121: 437-451. 10.1104/pp.121.2.437.
Buzgo M, Soltis DE, Soltis PS, Ma H: Towards a comprehensive integration of morphological and genetic studies of floral development. Trends Plant Sci. 2004, 9: 164-173. 10.1016/j.tplants.2004.02.003.
Becker A, Gleissberg S, Smyth DR: Floral and vegetative morphogenesis in California Poppy (Eschscholzia californica Cham.). Int J Plant Sci. 2005, 166: 537-555. 10.1086/429866.
Buzgo M, Chanderbali AS, Kim S, Zheng Z, G Oppenheimer D, Soltis PS, Soltis DE: Floral developmental morphology of Persea americana (Avocado, Lauraceae): The oddities of male organ identity. Int J Plant Sci. 2007, 168: 261-284. 10.1086/510297.
Gillaspy G, Ben-David H, Gruissem W: Fruits: a developmental perspective. Plant Cell. 1993, 5: 1439-1451. 10.1105/tpc.5.10.1439.
Smyth DR, Bowman JL, Meyerowitz EM: Early flower development in Arabidopsis. Plant Cell. 1990, 2: 755-767. 10.1105/tpc.2.8.755.
Bertin N, Genard M, Fishman S: A model for an early stage of tomato fruit development: cell multiplication and cessation of the cell proliferative activity. Ann Bot (Lond). 2003, 92: 65-72. 10.1093/aob/mcg111.
Joubes J, Phan T-H, Just D, Rothan C, Bergounioux C, Raymond P, Chevalier C: Molecular and biochemical characterization of the involvement of cyclin-dependent kinase A during the early development of tomato fruit. Plant Physiol. 1999, 121: 857-869. 10.1104/pp.121.3.857.
Giovannoni JJ: Genetic regulation of fruit development and ripening. Plant Cell. 2004, 16 (Suppl): S170-180. 10.1105/tpc.019158.
Angenent GC, Franken J, Busscher M, Colombo L, van Tunen AJ: Petal and stamen formation in petunia is regulated by the homeotic gene fbp1. Plant J. 1993, 4: 101-112. 10.1046/j.1365-313X.1993.04010101.x.
Colombo L, Franken J, Koetje E, van Went J, Dons HJ, Angenent GC, van Tunen AJ: The petunia MADS box gene FBP11 determines ovule identity. Plant Cell. 1995, 7: 1859-1868. 10.1105/tpc.7.11.1859.
de Martino G, Pan I, Emmanuel E, Levy A, Irish VF: Functional analyses of two tomato APETALA3 genes demonstrate diversification in their roles in regulating floral development. Plant Cell. 2006, 18: 1833-1845. 10.1105/tpc.106.042978.
Krol van der AR, Brunelle A, Tsuchimoto S, Chua NH: Functional analysis of petunia floral homeotic MADS box gene pMADS1. Genes Dev. 1993, 7: 1214-1228. 10.1101/gad.7.7a.1214.
Vandenbussche M, Zethof J, Royaert S, Weterings K, Gerats T: The duplicated B-class heterodimer model: whorl-specific effects and complex genetic interactions in Petunia hybrida flower development. Plant Cell. 2004, 16: 741-754. 10.1105/tpc.019166.
Vandenbussche M, Zethof J, Souer E, Koes R, Tornielli GB, Pezzotti M, Ferrario S, Angenent GC, Gerats T: Toward the analysis of the petunia MADS box gene family by reverse and forward transposon insertion mutagenesis approaches: B, C, and D floral organ identity functions require SEPALLATA-like MADS box genes in petunia. Plant Cell. 2003, 15: 2680-2693. 10.1105/tpc.017376.
Grandillo S, Ku HM, Tanksley SD: Identifying the loci responsible for natural variation in fruit size and shape in tomato. Theor Appl Genet. 1999, 99: 978-987. 10.1007/s001220051405.
Liu J, Van Eck J, Cong B, Tanksley SD: A new class of regulatory genes underlying the cause of pear-shaped tomato fruit. Proc Natl Acad Sci USA. 2002, 99: 13302-13306. 10.1073/pnas.162485999.
Xiao H, Jiang N, Schaffner E, Stockinger EJ, Knaap van der E: A retrotransposon-mediated gene duplication underlies morphological variation of tomato fruit. Science. 2008, 319: 1527-1530. 10.1126/science.1153040.
Cong B, Barrero LS, Tanksley SD: Regulatory change in YABBY-like transcription factor led to evolution of extreme fruit size during tomato domestication. Nat Genet. 2008, 40: 800-804. 10.1038/ng.144.
Frary A, Nesbitt TC, Frary A, Grandillo S, Knaap Evd, Cong B, Liu J, Meller J, Elber R, Alpert KB, et al: fw2.2: a quantitative trait locus key to the evolution of tomato fruit size. Science. 2000, 289: 85-88. 10.1126/science.289.5476.85.
Levy M, Wang Q, Kaspi R, Parrella MP, Abel S: Arabidopsis IQD1, a novel calmodulin-binding nuclear protein, stimulates glucosinolate accumulation and plant defense. Plant J. 2005, 43: 79-96. 10.1111/j.1365-313X.2005.02435.x.
Welty N, Radovich C, Meulia T, Knaap van der E: Inflorescence development in two tomato species. Can J Bot. 2007, 85: 111-118. 10.1139/B06-154.
Deikman J, Kline R, Fischer RL: Organization of ripening and ethylene regulatory regions in a fruit-specific promoter from tomato (Lycopersicon esculentum). Plant Physiol. 1992, 100: 2013-2017. 10.1104/pp.100.4.2013.
Giovannoni J: Molecular biology of fruit maturation and ripening. Annu Rev Plant Physiol Plant Mol Biol. 2001, 52: 725-749. 10.1146/annurev.arplant.52.1.725.
Klee HJ: Ethylene signal transduction. Moving beyond Arabidopsis. Plant Physiol. 2004, 135: 660-667. 10.1104/pp.104.040998.
Ge Y, Dudoit S, Speed T: Resampling-based multiple testing for microarray data analysis. Test. 2003, 12: 1-44. 10.1007/BF02595811.
Busi MV, Bustamante C, D'Angelo C, Hidalgo-Cuevas M, Boggio SB, Valle EM, Zabaleta E: MADS-box genes expressed during tomato seed and fruit development. Plant Mol Biol. 2003, 52: 801-815. 10.1023/A:1025001402838.
Hileman LC, Sundstrom JF, Litt A, Chen M, Shumba T, Irish VF: Molecular and phylogenetic analyses of the MADS-Box gene family in tomato. Mol Biol Evol. 2006, 23: 2245-2258. 10.1093/molbev/msl095.
Pnueli L, Hareven D, Rounsley SD, Yanofsky MF, Lifschitz E: Isolation of the tomato AGAMOUS gene TAG1 and analysis of its homeotic role in transgenic plants. Plant Cell. 1994, 6: 163-173. 10.1105/tpc.6.2.163.
Ampomah-Dwamena C, Morris BA, Sutherland P, Veit B, Yao JL: Down-regulation of TM29, a tomato SEPALLATA homolog, causes parthenocarpic fruit development and floral reversion. Plant Physiol. 2002, 130: 605-617. 10.1104/pp.005223.
Sablowski RW, Meyerowitz EM: A homolog of NO APICAL MERISTEM is an immediate target of the floral homeotic genes APETALA3/PISTILLATA. Cell. 1998, 92: 93-103. 10.1016/S0092-8674(00)80902-2.
Vrebalov J, Ruezinsky D, Padmanabhan V, White R, Medrano D, Drake R, Schuch W, Giovannoni J: A MADS-box gene necessary for fruit ripening at the tomato ripening-inhibitor (rin) locus. Science. 2002, 296: 343-346. 10.1126/science.1068181.
Leseberg CH, Eissler CL, Wang X, Johns MA, Duvall MR, Mao L: Interaction study of MADS-domain proteins in tomato. J Exp Bot. 2008, 59: 2253-2265. 10.1093/jxb/ern094.
Sessions A, Nemhauser JL, McColl A, Roe JL, Feldmann KA, Zambryski PC: ETTIN patterns the Arabidopsis floral meristem and reproductive organs. Development. 1997, 124: 4481-4491.
Liu Z, Franks RG, Klink VP: Regulation of gynoecium marginal tissue formation by LEUNIG and AINTEGUMENTA. Plant Cell. 2000, 12: 1879-1892. 10.1105/tpc.12.10.1879.
Roe JL, Nemhauser JL, Zambryski PC: TOUSLED participates in apical tissue formation during gynoecium development in Arabidopsis. Plant Cell. 1997, 9: 335-353. 10.1105/tpc.9.3.335.
Kuusk S, Sohlberg JJ, Long JA, Fridborg I, Sundberg E: STY1 and STY2 promote the formation of apical tissues during Arabidopsis gynoecium development. Development. 2002, 129: 4707-4717.
Alvarez J, Smyth DR: CRABS CLAW and SPATULA, two Arabidopsis genes that control carpel development in parallel with AGAMOUS. Development. 1999, 126: 2377-2386.
Crawford BCW, Ditta G, Yanofsky MF: The NTT gene is required for transmitting-tract development in carpels of Arabidopsis thaliana. Curr Biol. 2007, 17: 1101-1108. 10.1016/j.cub.2007.05.079.
Gremski K, Ditta G, Yanofsky MF: The HECATE genes regulate female reproductive tract development in Arabidopsis thaliana. Development. 2007, 134: 3593-3601. 10.1242/dev.011510.
Liljegren SJ, Ditta GS, Eshed Y, Savidge B, Bowman JL, Yanofsky MF: SHATTERPROOF MADS-box genes control seed dispersal in Arabidopsis. Nature. 2000, 404: 766-770. 10.1038/35008089.
Rajani S, Sundaresan V: The Arabidopsis myc/bHLH gene ALCATRAZ enables cell separation in fruit dehiscence. Curr Biol. 2001, 11: 1914-1922. 10.1016/S0960-9822(01)00593-0.
Liljegren SJ, Roeder AHK, Kempin SA, Gremski K, Østergaard L, Guimil S, Reyes DK, Yanofsky MF: Control of fruit patterning in Arabidopsis by INDEHISCENT. Cell. 2004, 116: 843-853. 10.1016/S0092-8674(04)00217-X.
Roeder AHK, Ferrándiz C, Yanofsky MF: The role of the REPLUMLESS homeodomain protein in patterning the Arabidopsis fruit. Curr Biol. 2003, 13: 1630-1635. 10.1016/j.cub.2003.08.027.
Ferrandiz C, Liljegren SJ, Yanofsky MF: Negative regulation of the SHATTERPROOF genes by FRUITFULL during Arabidopsis fruit development. Science. 2000, 289: 436-438. 10.1126/science.289.5478.436.
Pinyopich A, Ditta GS, Savidge B, Liljegren SJ, Baumann E, Wisman E, Yanofsky MF: Assessing the redundancy of MADS-box genes during carpel and ovule development. Nature. 2003, 424: 85-88. 10.1038/nature01741.
Torii KU, Mitsukawa N, Oosumi T, Matsuura Y, Yokoyama R, Whittier RF, Komeda Y: The Arabidopsis ERECTA gene encodes a putative receptor protein kinase with extracellular leucine-rich repeats. Plant Cell. 1996, 8: 735-746. 10.1105/tpc.8.4.735.
Bowman JL, Smyth DR: CRABS CLAW, a gene that regulates carpel and nectary development in Arabidopsis, encodes a novel protein with zinc finger and helix-loop-helix domains. Development. 1999, 126: 2387-2396.
Kerstetter RA, Bollman K, Taylor RA, Bomblies K, Poethig RS: KANADI regulates organ polarity in Arabidopsis. Nature. 2001, 411: 706-709. 10.1038/35079629.
Eshed Y, Baum SF, Bowman JL: Distinct mechanisms promote polarity establishment in carpels of Arabidopsis. Cell. 1999, 99: 199-209. 10.1016/S0092-8674(00)81651-7.
McConnell JR, Emery J, Eshed Y, Bao N, Bowman J, Barton MK: Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots. Nature. 2001, 411: 709-713. 10.1038/35079635.
Alves-Ferreira M, Wellmer F, Banhara A, Kumar V, Riechmann JL, Meyerowitz EM: Global expression profiling applied to the analysis of Arabidopsis stamen development. Plant Physiol. 2007, 145: 747-762. 10.1104/pp.107.104422.
Gomez-Mena C, de Folter S, Costa MM, Angenent GC, Sablowski R: Transcriptional program controlled by the floral homeotic gene AGAMOUS during early organogenesis. Development. 2005, 132: 429-438. 10.1242/dev.01600.
Wellmer F, Riechmann JL, Alves-Ferreira M, Meyerowitz EM: Genome-wide analysis of spatial gene expression in Arabidopsis flowers. Plant Cell. 2004, 16: 1314-1326. 10.1105/tpc.021741.
Dharmasiri N, Dharmasiri S, Jones AM, Estelle M: Auxin action in a cell-free system. Curr Biol. 2003, 13: 1418-1422. 10.1016/S0960-9822(03)00536-0.
Woodward AW, Bartel B: Auxin: regulation, action, and interaction. Ann Bot. 2005, 95: 707-735. 10.1093/aob/mci083.
Helliwell CA, Sullivan JA, Mould RM, Gray JC, Peacock WJ, Dennis ES: A plastid envelope location of Arabidopsis ent-kaurene oxidase links the plastid and endoplasmic reticulum steps of the gibberellin biosynthesis pathway. Plant J. 2001, 28: 201-208. 10.1046/j.1365-313X.2001.01150.x.
Serrani JC, Sanjuan R, Ruiz-Rivero O, Fos M, Garcia-Martinez JL: Gibberellin regulation of fruit set and growth in tomato. Plant Physiol. 2007, 145: 246-257. 10.1104/pp.107.098335.
Ueguchi-Tanaka M, Ashikari M, Nakajima M, Itoh H, Katoh E, Kobayashi M, Chow TY, Hsing YI, Kitano H, Yamaguchi I, et al: GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin. Nature. 2005, 437: 693-698. 10.1038/nature04028.
Umezawa T, Okamoto M, Kushiro T, Nambara E, Oono Y, Seki M, Kobayashi M, Koshiba T, Kamiya Y, Shinozaki K: CYP707A3, a major ABA 8'-hydroxylase involved in dehydration and rehydration response in Arabidopsis thaliana. Plant J. 2006, 46: 171-182. 10.1111/j.1365-313X.2006.02683.x.
Foster R, Mattsson O, Mundy J: Plants flex their skeletons. Trends Plant Sci. 2003, 8: 202-204. 10.1016/S1360-1385(03)00061-X.
Teale WD, Paponov IA, Palme K: Auxin in action: signalling, transport and the control of plant growth and development. Nat Rev Mol Cell Biol. 2006, 7: 847-859. 10.1038/nrm2020.
Zahn LM, Kong H, Leebens-Mack JH, Kim S, Soltis PS, Landherr LL, Soltis DE, dePamphilis CW, Ma H: The evolution of the SEPALLATA subfamily of MADS-box genes: a preangiosperm origin with multiple duplications throughout angiosperm history. Genetics. 2005, 169: 2209-2223. 10.1534/genetics.104.037770.
Brukhin V, Hernould M, Gonzalez N, Chevalier C, Mouras A: Flower development schedule in tomato Lycopersicon esculentum cv. Sweet cherry. Sex Plant Reprod. 2003, 15: 311-320.
Mandel MA, Gustafson-Brown C, Savidge B, Yanofsky MF: Molecular characterization of the Arabidopsis floral homeotic gene APETALA1. Nature. 1992, 360: 273-277. 10.1038/360273a0.
Weigel D, Alvarez J, Smyth DR, Yanofsky MF, Meyerowitz EM: LEAFY controls floral meristem identity in Arabidopsis. Cell. 1992, 69: 843-859. 10.1016/0092-8674(92)90295-N.
Vriezen WH, Feron R, Maretto F, Keijman J, Mariani C: Changes in tomato ovary transcriptome demonstrate complex hormonal regulation of fruit set. New Phytol. 2008, 177: 60-76.
Galpaz N, Wang Q, Menda N, Zamir D, Hirschberg J: Abscisic acid deficiency in the tomato mutant high-pigment 3 leading to increased plastid number and higher fruit lycopene content. Plant J. 2008, 53: 717-730. 10.1111/j.1365-313X.2007.03362.x.
Riou-Khamlichi C, Huntley R, Jacqmard A, Murray JAH: Cytokinin activation of Arabidopsis cell division through a D-type cyclin. Science. 1999, 283: 1541-1544. 10.1126/science.283.5407.1541.
Knaap van der E, Sanyal A, Jackson SA, Tanksley SD: High-resolution fine mapping and fluorescence in situ hybridization analysis of sun, a locus controlling tomato fruit shape, reveals a region of the tomato genome prone to DNA rearrangements. Genetics. 2004, 168: 2127-2140. 10.1534/genetics.104.031013.
Jensen WA: Botanical Histochemistry: Principles and Practice. San Francisco: W H Freeman; 1962.
Irizarry RA, Bolstad BM, Collin F, Cope LM, Hobbs B, Speed TP: Summaries of Affymetrix GeneChip probe level data. Nucl Acids Res. 2003, 31: e15-10.1093/nar/gng015.
Edgar R, Domrachev M, Lash AE: Gene expression omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002, 30: 207-210. 10.1093/nar/30.1.207.
Wan CY, Wilkins TA: A modified hot borate method significantly enhances the yield of high-quality RNA from cotton (Gossypium hirsutum L.). Anal Biochem. 1994, 223: 7-12. 10.1006/abio.1994.1538.
The authors thank J. Moyseenko and L. Duncan for plant care and the Molecular and Cellular Imaging Center staff for technical help. We thank Drs. S. Hogenhout and S. Kamoun for collaborations on the Nimblegen microarray experiments. We also thank Dr. M. Buzgo for advice, and Drs JC Jang and M. Jones for critical reading of this manuscript. This work was funded by National Science Foundation grants DBI 0227541 to EVDK.
HX and NW conducted the experiments on ethylene and seed germination, and fruit shape mediated by SUN. HX conducted the Northern blots and together with JH and DL the transcript profiling analysis. CR and TM conducted the floral landmark study. NW and TM conducted the fruit landmark study. EvdK supervised the project and conducted the pollination experiment. HX, TM, NW and EvdK wrote the paper with editorial comments from the other authors.
Han Xiao, Cheryll Radovich, Nicholas Welty contributed equally to this work.
Electronic supplementary material
Additional file 1: Differentially expressed genes at 10 day pre-anthesis flower, anthesis flower and 5 dpa fruit. The spreadsheet contains all the transcripts that were differentially expressed between any of the three stages: 10 days pre-anthesis flower buds (pre), anthesis flowers (ant) and 5 dpa fruit (post). (XLS 428 KB)
Additional file 4: Plot of RMA intensities between LA1589 NILs that differ at sun. Background collection and normalization of hybridization signals were performed on the 18 arrays using the Robust Multichip Average algorithm (RMA). (A) Plot of RMA values for flower buds at 10 days preanthesis (Bud). (B) Plot of RMA values for anthesis-stage flower (Flower). (C) Plot of RMA values for 5 dpa fruit (Fruit). Data shown in the graphs are averaged log2(RMA intensities) of the three biological replicates. The number in each plot is the Pearson's coefficient (R) between the two genotypes, LA1589ee, homozygous LA1589 NILs with SUN, and LA1589pp, homozygous for the wild-type allele. (DOC 192 KB)
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Xiao, H., Radovich, C., Welty, N. et al. Integration of tomato reproductive developmental landmarks and expression profiles, and the effect of SUN on fruit shape. BMC Plant Biol 9, 49 (2009) doi:10.1186/1471-2229-9-49
- Fruit Development
- Tomato Fruit
- Floral Meristem
- Fruit Growth
- Fruit Shape