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HLA-B新等位基因B~*4608的核苷酸序列分析
引用本文:何俊俊,吕沁风,章伟,韩浙东,王炜,朱发明,严力行. HLA-B新等位基因B~*4608的核苷酸序列分析[J]. 中国输血杂志, 2007, 20(1): 7-9
作者姓名:何俊俊  吕沁风  章伟  韩浙东  王炜  朱发明  严力行
作者单位:浙江省血液中心,卫生部血液安全研究重点实验室,浙江杭州,310006
摘    要:目的分析1个HLA-B位点有异常反应格局样本的核苷酸序列。方法采用DNA快速抽提试剂盒抽提样本基因组DNA,PCR方法扩增先证者HLA-B基因的第1-8外显子,PCR产物直接经TOPO TA克隆到质粒载体中以获得单链,对克隆所得产物进行HLA-B基因第2、3、4外显子双向测序分析。结果先证者样本克隆测序得到两个等位基因,其中1个等位基因为B*5502,另1个经Blast验证为新等位基因,其序列已递交Genbank(DQ177521,DQ177522,DQ177523)。与最接近的B*4601等位基因序列相比,新等位基因在第3外显子上有2个核苷酸不同,即第538位T→C和第539位G→T,并由此导致1个氨基酸改变:第156位色氨酸→亮氨酸。结论该新HLA-B等位基因已WHO HLA因子命名委员会正式命名为HLA-B*4608。

关 键 词:HLA-B/B*4608  DNA,基因组  PCR-SSO克隆测序分析
文章编号:1004-549X(2007)01-0007-03
收稿时间:2006-06-27
修稿时间:2006-12-20

Sequences analysis for a novel HLA-B allele:HLA-B*4608
HE Junjun, LUE Qinfeng ,ZHANG Wei,et al.. Sequences analysis for a novel HLA-B allele:HLA-B*4608[J]. Chinese Journal of Blood Transfusion, 2007, 20(1): 7-9
Authors:HE Junjun   LUE Qinfeng   ZHANG Wei  et al.
Affiliation:BloodCenter of Zhejiang Province, Key Laboratory of Blood Safety Research of Ministry of Health, Hangzhou 310006, China
Abstract:Objective To analyze the nucleotide sequences of novel allele HLA-B*4608. Methods Genomic DNA of the proband was extracted from whole blood by the commercial DNA extraction kit. The HLA-B exons 1-8 of the proband was amplified and the amplified product was cloned by TOPO TA cloning sequencing kit to split the two alleles apart. Both strands of exons 2, 3 and 4 of chosen colonies were sequenced. Results The sequencing results showed HLA-B alleles of the proband as B*5502 and a new allele as proved by blast search. The sequences of the novel allele have been submitted to Genbank(DQ177521,DQ177522,DQ177523). The new allele is similar to HLA-B*4601 except for two nucleotide substitutions in exon 3: T to C at nucleotide position 538 and G to T at nucleotide position 539. These result in an amino acid substitution at codon 156 from W to L. Conclusion This allele is a novel allele and has been officially named B*4608 by the WHO Nomenclature Committee.
Keywords:HLA-B/B*4608  DNA  PCR-SSO
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