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Table 2 Details of the primers used

From: Genetic diversity of the conserved motifs of six bacterial leaf blight resistance genes in a set of rice landraces

Primer name

Gene

Protein

ANN temp

Exon no.

Start (bp)

End (bp)

Forward primer

Reverse primer

BDTG 1

Xa1

P Loop

59.8

1

3113

3621

5 ́-ATTAATCCACGACGACCAGG – 3 ́

5 ́-GTAGCACAAGCACCTCCTCC – 3 ́

BDTG 2

Kinase 2 & 3

60

2

3602

4031

5 ́-GAGGAGGTGCTTGTGCTACAG – 3 ́

5 ́-GGCACTGGCATTACCTTGAT – 3 ́

BDTG 3

TRANS MEM

59.5

3

4681

5200

5 ́-GGTGAGGGTGCATCAAATG – 3 ́

5 ́-TTATTCCTTCGTGGCTCTGG – 3 ́

BDTG 4

59.8

3

5167

5698

5 ́-TTGGATCATGTCTCCAACCA – 3 ́

5 ́-ACTTCAGCGCTTGCATGAT – 3 ́

BDTG 5

59.8

3

5710

6587

5 ́-CATCTATCCAACCCCTTACAGC – 3 ́

5 ́-CAAGCTTGTTCATGGATTTCAA – 3 ́

BDTG 6

60.2

3

6621

8399

5 ́-TAGAACTCAGGAGGAGGCATGT – 3 ́

5 ́-TGATTGCGGAAGGATACACA – 3 ́

BDTG 7

60.2

3

8370

8940

5 ́-AGATGGAATGTGTATCCTTCCG – 3 ́

5 ́-GGAAGGATACACCTTCCATTTTC – 3 ́

BDTG 8

LRR

59.5

4

25981

26700

5 ́-GATGGCTCCTACCGCTATCA – 3 ́

5 ́-GATGTGCAAGAATGGAGCTG – 3 ́

BDTG 9

60.9

4

26662

27231

5 ́-CTCAAATTTAGTGTCTCTGCAGCTC – 3 ́

5 ́-TCCGCGATAGTTAAGCTCTAGG – 3 ́

BDTG 10

60

4

27182

27917

5 ́-TCTGCAAGCACCTCACCTC – 3 ́

5 ́-ATGCATTGGAGCGGATTG – 3 ́

BDTG 11

Xa5

TF II A

59.9

1

406048

406306

5 ́-TTCGAGCTCTACCGGAGGT – 3 ́

5 ́-AGAAACCTTGCTCTTGACTTGG – 3 ́

BDTG 12

60.2

2

411394

411535

5 ́-TGTTCTTTTCTCAGGGCCAC – 3 ́

5 ́-AGTTTGGAATCACAGGCCAC – 3 ́

BDTG 13

Xa26

RECP Kinase

59.5

1

1500

2094

5 ́-GATGCATACTCTTGCTGCCA – 3 ́

5 ́-CAAGACTGTGCAACCCCTG – 3 ́

BDTG 14

60.1

1

2043

2695

5 ́-ACCAGCTATACGGTCCAATCC – 3 ́

5 ́-GCAAGATGCAACCATGAAAGT – 3 ́

BDTG 15

59.6

1

2716

3332

5 ́-CTATTCCTGCTTCTCTTGGCA – 3 ́

5 ́-AGCCTGACGATTTTATCAAGATG – 3 ́

BDTG 16

59.6

1

3320

3956

5 ́-CATCTTGATAAAATCGTCAGGCT – 3 ́

5 ́-GGTTGCACGAAGAAGCTCAT – 3 ́

BDTG 17

59.8

1

3968

4492

5 ́-CGATGATAGCATGTTGGGC – 3 ́

5 ́-AAAAACTATTAAGTACCTGGTGCCAT– 3 ́

BDTG 18

59.9

1

4574

5141

5 ́-TGAGCAGAGTATGGGACTCTAGG – 3 ́

5 ́-ACACCAACTATAAATTGTTGCAGAAC – 3 ́

BDTG 19

Xa27

 

59.9

1

1518

1909

5 ́-GAAGCCACACACACTGAGACA – 3 ́

5 ́-CGGAGGAGAACTAGAGAGACCA – 3 ́

BDTG 20

Xa21

Signal

59.7

1

8

208

5 ́-CACTCCCATTATTGCTCTTCG – 3 ́

5 ́-ACACAACACCCACCCATGT – 3 ́

BDTG 21

LRR

61.8

2

260

760

5 ́-GCTCCTCCAACCTGTCCG – 3 ́

5 ́-TAAACGCTCTTAGAGACGAAAGGT – 3 ́

BDTG 22

59.7

2

723

1314

5 ́-CAATTCTATCTGGAACCTTTCGTC – 3 ́

5 ́-ACCGCTCAAGTTGTTTTCGT – 3 ́

BDTG 23

60

2

1279

1880

5 ́-GGCATTCTACTCGCCTACGA – 3 ́

5 ́-GCATTGCCTTGGATTGAGAT – 3 ́

BDTG 24

Charged

59.8

3

1913

2620

5 ́-TGCCTCGATGTTGTCCATTA – 3 ́

5 ́-TCAATGAGGTCCCATCAACA – 3 ́

BDTG 25

Kinase

60.1

4 & 5

2651

3919

5 ́-AGGGACAATTGGCTATGCAG – 3 ́

5 ́-AGAATTCAAGGCTCCCACCT – 3 ́

BDTG 26

Xa21(A1)

LRR

59.8

1

4802

5082

5 ́-TGTTGTTCTCTGCGCTGC – 3 ́

5 ́-CGTCCTGAGGAAGGATAGGTT – 3 ́

BDTG 27

59.6

1

5051

5459

5 ́-CATCGCTGGGCAACCTAT – 3 ́

5 ́-TTGGACACGACTTCAAATATGG – 3 ́

BDTG 28

  

59.6

1

5406

5803

5 ́-CCCAGATCCTATTTGGAACATC – 3 ́

5 ́-TGGAAACAGAATCAGGGAGG – 3 ́

BDTG 29

59.9

1

5763

6173

5 ́-AGGTTGCAAATTTGGTGGAG – 3 ́

5 ́-GGAATGCTAAATATTTCAATGGGA – 3 ́

BDTG 30

60.2

1

6140

6531

5 ́-TAGGGCAAATTCCCATTGAA – 3 ́

5 ́-AAAACACCATTGGTTGGCA – 3 ́

BDTG 31

59.9

1

6484

6889

5 ́-CTTTCGTTCAACAGCTTCCAC – 3 ́

5 ́-CACCATCTTGACTATCAAATTCTCC – 3 ́

BDTG 32

59.9

1

6859

7422

5 ́-CTTTCGTTCAACAGCTTCCAC – 3 ́

5 ́-CAATGAAAGGAGGTAGACATAAACAGT – 3 ́

BDTG 33

SNAP

60.2

2

7395

7610

5 ́-ACTGTTTATGTCTACCTCCTTTCATTG – 3 ́

5 ́-AATAGATTTGCTACGGTCGAACA – 3 ́

BDTG 34

Kinase

59.7

3

7718

8081

5 ́-TTTGTTATGGAATTCTAGTGTTGGAA – 3 ́

5 ́-CCAACATAACATCAGCATGTCTC – 3 ́

  1. Gene - Resistance genes from which the primers were designed; Protein - Protein coded by the DNA sequence amplified by the corresponding primer; Ann Temp – Annealing Temperature of the respective primer pair; Exon no. - Exon of the original gene from which primer pair was designed; Start – expected start point of the amplification product with respect to the original gene sequence, End – Expected end point of the amplification product with respect to the original gene sequence.