CD31/PECAM-1 genotyping and haplotype analyses show population diversity

被引:10
|
作者
Robbins, F. -M.
Hartzman, R. J.
机构
[1] Georgetown Univ, Med Ctr, CW Bill Young Marrow Donor Recruitment & Res Prog, Dept Pediat, Washington, DC 20007 USA
[2] Naval Med Res Ctr, CW Bill Young Marrow Donor Recruitment & Res Prog, Silver Spring, MD USA
来源
TISSUE ANTIGENS | 2007年 / 69卷 / 01期
关键词
CD31; alleles; haplotype tag single nucleotide polymorphisms; molecular haplotyping; polymerase chain reaction-sequence-specific oligonucleotide probing; single nucleotide polymorphism frequencies;
D O I
10.1111/j.1399-0039.2006.00722.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Using direct sequencing of complementary DNA products, the sequences of human CD31 from exon 1 through exon 16 of 179 individuals (139 unrelated) were systematically examined. Of the 14 biallelic single nucleotide polymorphic sites detected, 7 polymorphic sites involved amino acid substitution. These 14 polymorphic sites yielded 18 observed CD31 alleles and 9 predicted CD31 polypeptide sequences. Based on molecular haplotyping and family pedigree analysis, linkage disequilibrium among some single nucleotide polymorphic sites was observed. Single nucleotide polymorphism frequencies between populations were also measured using dot-blot hybridization with DNA or peptide nucleic acid probes.
引用
收藏
页码:28 / 37
页数:10
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