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Table 1 Primers and PCR conditions for amplifying and sequencing MRP 1

From: Nucleotide sequence analyses of the MRP 1 gene in four populations suggest negative selection on its coding region

Exons

Primer Direction

Length (bp)

Primer Sequence (5' – 3')

Amplicon Length(bp)

Additional Primer For Sequencing

Tm

Exon 1

Forward

22

GCATTTGAAAAGTGGTCGCAGG

688

 

59

 

Reverse

20

TCCGCAGGAACTGAGTCACC

   

Exon 2

Forward

20

GCAGAAGACACCACATACCT

510

 

60

 

Reverse

20

AGAAGAAGGAACTTAGGGTC

   

Exon 3

Forward

19

GCATGGTGACCAGACAAAC

501

 

60

 

Reverse

19

CTCCAGCTGATCATTGCCT

   

Exon 4

Forward

21

ACGTGGTCCATTAAGAAATAG

571

 

61

 

Reverse

20

GACTTCTACACAAGCCAGAG

   

Exon 5

Forward

19

CCCAGCCCCAGAATGTGAT

358

 

58

 

Reverse

18

CCCCAGCCACATCTAAGC

   

Exon 6

Forward

22

TGTTGTATTGTGGTTGCACATG

383

 

60

 

Reverse

20

GAGCTGAGCATGTTCATTCG

   

Exon 7

Forward

20

TCCCTAAGTCTTTTGTATGC

574

AAGCCATTTTTCCTGCATGAC (forward)

61

 

Reverse

19

TACCCCATTTGGCAGAAAA

   

Exon 8

Forward

20

AGAGAGCTTAAGGACCTTGT

591

 

59

 

Reverse

19

TATGAGCCCACTTCAGGAC

   

Exon 9

Forward

19

CGTGTTCCCTATGCAATTC

602

 

59

 

Reverse

18

CCTGCCACCTAAGGTCAC

   

Exon 10

Forward

18

TCCTGGGCAGACAGATAG

439

 

61

 

Reverse

18

TGAACCACAGCCGGAACT

   

Exon 11

Forward

19

GCTTGGGAGAAAGGAGCGT

452

 

61

 

Reverse

19

TGAGTCCAACTGGCAGGCA

   

Exon 12

Forward

20

TAATAGACGGTGAAGTTGAG

743

ATGAAGAGCAAAGACAATCG (forward)

61

 

Reverse

20

AAGTAATTCTCTTGCCTCAG

   

Exon 13

Forward

21

GTCGTTGATTTATCCAGTTCA

523

 

61

 

Reverse

20

CTTTCTTTCAGGCATGACCA

   

Exon 14

Forward

20

TCTGAAATACCTTTTGTGGG

627

 

60

 

Reverse

19

GGTCAAAGCCTTGGAAAGT

   

Exon 15

Forward

21

TTACAAGGACAAAGCTGCTTG

475

 

60

 

Reverse

19

TGTATCTGCACCCATTGTC

   

Exon 16

Forward

20

GTTTAGTACAGTCTTGCCTT

463

 

60

 

Reverse

19

CCAAAATCCTGCCTTCTAG

   

Exon 17

Forward

21

GTGGGCCAGCTGTTGTCTCGT

441

 

61

 

Reverse

20

AGTGAGACCTGAGCCACACC

   

Exon 18

Forward

18

CGTATTGTGAGTCTCAAG

596

TACCCATTACCACAACTG (reverse)

61

 

Reverse

18

TTTTCCGACCCCTCTACC

   

Exon 19

Forward

18

GAGTTTTGCCCACCAGGT

462

 

61

 

Reverse

19

GGTGGTTTTCCACATTGCT

   

Exon 20

Forward

18

TATGCCCTTTCCCTCATG

758

 

61

 

Reverse

18

GAGCAAAGACCCACACCA

   

Exon 21

Forward

19

CTGGAGAGTGACATGGTGG

504

 

61

 

Reverse

20

GGGTGACCCTGAGTAAGTCA

   

Exon 22

Forward

20

GTTGAATAGCTAAAGGGGAG

599

 

61

 

Reverse

19

TGTAAAATGGGCACACTGG

   

Exon 23

Forward

20

ATGCCTGGTTCATCATTATT

514

 

58

 

Reverse

20

CTTTAGGTAACACTGGTATA

   

Exon 24

Forward

20

AGCGTGAGCTATTATTGTCA

727

 

61

 

Reverse

19

ACTCAATAGCAGAGTCGGT

   

Exon 25, 26

Forward

19

CCCATTGTGCATGTTTTGA

1442

AGATGCAGCTAAAGCAGTTC*

GTGACTGATGGGGTTTCG**

61

 

Reverse

20

AAAGACTGGACAAGCGTTAA

   

Exon 27

Forward

22

ACCTACTATGTGCTCTGAGCCC

693

 

61

 

Reverse

20

TACTGCCACAGTCCACTCCC

   

Exon 28

Forward

18

CGAGTCATTCCTTTTGGG

493

 

61

 

Reverse

20

GTAGGGCCAAATGTATGTTT

   

Exon 29

Forward

18

AAGGAGCTCTGATACCCC

405

 

61

 

Reverse

19

GGACAAATGGTCATCTGGG

   

Exon 30

Forward

19

CTCCCAAAGTGCTCAGATT

706

 

61

 

Reverse

19

GAAATGCTTGAACCCCAGA

   

Exon 31

Forward

21

TCTGAATGTAATGGAACAGTG

1677

 

61

 

Reverse

21

GGAAGAGCATCAGTAACTAAA

   
  1. *reverse primer for Exon 25, **forward primer for Exon 26