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Table 2 Sequence and location of PCR and sequencing primers

From: Analysis of single-nucleotide polymorphisms (SNPs) in human CYP3A4 and CYP3A5 genes: potential implications for the metabolism of HIV drugs

PCR name

Region

Primers sequence (forward and reverse)

Location of primers

PCR product size

PCR annealing temperature (°C)

CYP3A4 gene

     

A

5′ Proximal Region

A1: GGTCTGTCTGTCTGGGTATGC

 

296

61

  

A2: CTCACCACACACTGACCTGCT

   

B

EXON 1 (nt 1–71)

B1: AGAACCCAGAACCCTTTGGAC

1

1137

59

  

B2: GTGCTCCTCTATCTGTGAGTA

78

  

C

EXON 2 (nt 4004–4097)

C1: GCTCTCAGTGACCCTCTGTG

3532

1192

59

  

C2: AACCCCTTTGTTCTGTCTCTCA

4723

  

D

EXON 3 (nt 6009–6061)

D1: CCCTGGTGTCTGTACTTTCCA

5529

1200

59

  

D2: TCCCAGCCTAGTTCAGACTGT

6728

  

E

EXON 4 (nt 11502–11601)

E1: ATATCCACGTATGCACCACCC

11185

841

59

  

E2: GAGCCACATGGAGACAGAGT

12025

  

F

EXONS 5/6 (nt 13956–14069) (nt 14335−14423)

F1: CGACATCAGGGTCTCCTGAAC

13720

933

59

  

F2: GATATGTAAACCCTGGCCCCT

14652

  

G

EXON 7 (nt 15689–15837)

G1: CTGTTTGTCTGTCTTGACTGGA

15585

998

61

  

G2: GCTGTTCAAGAAATAGTAGGTAGTC

16582

  

H

EXON 8 (nt 16932–17059)

H1: TTGAGCTTCAGATTATGATTTGGG

16593

956

60

  

H2: CTGGCTATCATGTGAGATGGC

17548

  

I

EXON 9 (nt 17744–17810)

I1: AGCCATCTCACATGATAGCCA

17527

990

57

  

I2: CTTGGTGGCTTGTAATTGACC

18516

  

J

EXON 10 (nt 20166–20326)

J1: TGGGGGAGAGTACTACCTCATA

19785

952

60

  

J2: AAGAGCCAATTCCTGTGTCCAT

20736

  

K

EXON11 (nt 21912–22138)

K1: TTCCCGAATGCTTCCCACCT

21691

917

59

  

K2: ATGCTACTGTACCGATGTAATGC

22607

  

L

EXON 12 (nt 23198–23360)

L1: GGGGTGGCCCCTAAGTAAGA

23109

910

57

  

L2: TTGGGTTGAAAAGGAGCCCA

24018

  

M

EXON 13 (nt 25950–26502)

M1: TGACTCTTCAAAAACAGTTTGCCA

25518

1099

59

  

M2: AGTTCTGACAAAGGCCCCAC

26502

  

CYP3A5 gene

     

N

EXON 1 (5001–5173)

N1: TAGAATGAAGGCAGCCATGGAG

4723

1032

60

  

N2: GGGGATTTTCAGGGGCATGG

5774

  

O

EXON 2 (8791–8884)

O1: GCTGGTTCTTCTGCACACAATC

8022

964

61

  

O2: GAAACCTCAGAACTCCCTCCC

8985

  

P

EXON 3 (10414–10466)

P1: ATGGAGAGTGGCATAGGAGAT

9878

1177

59

  

P2: TGTGGTCCAAACAGGGAAGAGAT

11054

  

Q

EXON 4 (12320–12419)

Q1: TGTCACCAGGTATCGAGGTCT

11062

1367

60

  

Q2: GATGCTTACCCTTCGATTTGTGA

12428

  

R

EXONS 5/6 (17934–18047) (18310–18398)

R1: CGCCCCACATACACTCAGAA

17746

1184

57

  

R2: GGCTTGCTCTACACATAGCAT

18929

  

S

EXON 7 (19685–19833)

S1: ATAGGGCCAGCTCCATCACTG

19492

1193

60

  

S2: TTCTGAGTCTTTGGAGTGACCA

20684

  

T

EXONS 8/9 (20904–21031) (22117–22183)

T1: GGCCTGAAAGAAGGGCAAAC

20750

1478

57

  

T2: TCTTAGTGTCCCCGCCAGTA

22228

  

U

EXON 10 (24340–24500)

U1: AGGATCATTCAAGGCACACACC

24009

1179

61

  

U2: GCCTTGCTGCTGCCTTGCAG

25188

  

V

EXON 11 (32220–32446)

V1: ACCTACCTATGATGCCGTGG

32225

880

57

  

V2: GAGGACCTGTGCTGTCTTGT

33104

  

W

EXON 12 (34767–34926)

W1: GCAGGATTTCAATGACCAGCC

34619

1173

59

  

W2: CCCCCTGCCTGAATACACAC

35792

  

Y

EXON 13 (36599–36809)

Y1: GGGTTCAACTGGGAAGGGTT

36118

1058

57

  

Y2: GTGTGCAGGATGGCATCAGA

37175

  
  1. PCR reactions are named in alphabetical order. The same primers are used for PCR and sequencing reactions.