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Table 3 Markers used in the study

From: Identification of single nucleotide polymorphism markers associated with resistance to bruchids (Callosobruchus spp.) in wild mungbean (Vigna radiata var. sublobata) and cultivated V. radiata through genotyping by sequencing and quantitative trait locus analysis

Name

Chromosome

Position

Forward primer

Reverse primer

Enzyme

Resistant allele fragment size

Susceptible allele fragment size

Reference

dCAPS2

3

3:10,431,528

CCTCCTCTGTTGGGAAATCA

TCTGAAGGCCTGTGTTAAGCT

Hind III

307

286 21

this study

dCAPS3

4

4:15,255,162

AGTACGGCCTCAAACAGTGG

GAAAATTACAATCAAATGGAGCT

SacI

303

283 20

this study

CAPS1

5

5:5,178,332

ACTTCACTGGGTGGACTTGC

ATTCTCAGGCATGGTCAAGG

TaqI

89 364

453

this study

CAPS2

5

5: 5,179,402

AGGTGAAATTGGTTGGAAGG

CCCATGTCAGAAGCATCATC

Hpy 188III

104 129 43 14 37

104 172 14 37

this study

dCAPS1

5

5,454,538

AGCTGTGGAATGACGACTAG

TTACAACACCCAGTGCGTTC

SPE1

324

304 20

this study

CAPS3

5

5: 5,622,070

TGCTCAGCTGCTATACCAAGA

CACAATGCCTGATGGAGAGA

XcmI

46 398

444

this study

CAPS4

5

5: 5,662,479

GAACCAGTTCAAGCGACTCC

CGAACTTAGAGGCCAAAACG

BanI

108 193

301

this study

CAPS6

5

5:5,730,691

CTGAATGGGTTTATGCGTTG

ATCAATGGCCCCTCTCTTTT

PsiI

306

139 167

this study

CAPS12

5

5:5,953,917

TGCATGTCAACGAAAACTCA

GTAGAGGGGGTTTTCCGAAG

TaqI or HinfI

188 (190) 122 (120)

310

this study

CAPS13

5

5:5,974,663

CGCAGCGAATGTTATCACTG

TTGCTGTGAAATTGCAGCTC

TaqI

221 180

401

this study

CAPS8

5

5:6,992,170

CGCCCTCCGTGTATTCTAAA

GGCTGCTTCACTTACCAAGC

BstYI

419

330 89

this study

CAPS14

5

5:6,066,948

CCGAGCATTGAGGTTGGTAT

CTAAGGCGAGCTGCTGAAGT

NheI

322

165 157

this study

CAPS9

5

5:7,212,649

TGGCATGAAATGAGTTAAAAGTG

TCCTGAACTTGGGGTTATGG

RsaI

66 366

66 173 193

this study

CAPS11

5

5:7,551,254

ACAAGCTGATGGGCAAACTC

GACGGATCCGAGTGTTTGTT

AseI

100 238

100 113 125

this study

TETRA1

1

26,370,595

O:CCGAAGATGTGTGATTCATG

I:GACGATACTTGTCCAGATAT

O:GAAGGGATTTTGTTAGGAGT

I:AGCACTCAAGATGAAAGTGATC

-

  

this study

TETRA2

2

23,741,639

O:ACTATCTGACCGAAAGGAA

I:TTGGTACCAAATTCTGCACT

O:ATCTGCTGACAGGAGAATTCA

I:ATCTTACGGTGAAGGACATT

-

  

this study

TETRA3

7

13,713,780

O:TAGCTGGTCCGTGTACTTTA

I:TTTCCATTGTGGGTCGTGGAGT

O:GGAACTATGCTTTGGGACTT

I:ATTCTTGTAGCATCATCAAAACT

-

  

this study

TETRA4

10

3,159,416

O:ATACTGGAGGGTTGTTTCTA

I:TAAGCGTGCGCAGCCATAAACAAG

O:CGGTCTCAGAATCATAGTCTTG

I:GGGTTTTTTCGGAAATTCAAAG

-

  

this study

DMB-SSR-158

5

5:5,597,891 - 5:5,590,645a

TGGAAAATTTGCAGCAGTTG

ATTGATGGAGGGCGGAAGTA

 

300-400

[11, 12]

779

5

7351532-7351612

CTAATAAATCATCTATACgTCTCTC

ATTgCTATTTAgCgAATAATAgTAC

  

[13]

OPW 02a4

5

6743545 – 6745026a

CCAAAggAgTCgAgTgAAACT

CAACAACCCTTCCTCTATCTC

 

400 – 1,100

[13]

Vr34480

?

?

AATTCTTgATTggTCCACATg

AAAAAATTACACCTCgTTCg

 

500

[13]

MB-87

?

Fwrd:3:11,421,121

TCCCTTGTGGGAGATCCT

CTTTGCCACACTCCTTGC

 

~300

[21]

4:15,255,162

5:5,602,099

Rev: −b

  1. O: outer primer, I: inner primer for tetra primer, a) the predicted fragment length according to the reference sequence is larger than the fragment obtained in both populations. b) forward and reverse primer do not match to a common scaffold or chromosome of the reference sequence