Suppr超能文献

[广东地区地中海贫血基因的基因型及β-珠蛋白基因的多态性]

[Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].

作者信息

Liu Ling, Jiang Wei-ying, Xu Shi-yan, Chen Juan, Chen Lu-ming, Tian Qiu-hong, Wang Ji-cheng

机构信息

Department of Medical Genetics, Sun Yet-Sen University Zhongshan School of Medicine, Guangzhou 510080, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2013 Jul;34(7):595-9. doi: 10.3760/cma.j.issn.0253-2727.2013.07.008.

Abstract

OBJECTIVE

To understand the genotype of α and β-globin, as well as the polymorphism of β-globin gene in Cantonese in recent years, and to provide an effective genetic diagnosis for thalassemia (thal).

METHODS

The single-tube complex PCR was used to detect 3 types of deletional α-thal, reverse dot blotting (RDB)/PCR to detect 3 kinds of undeletional α-thal-αCS, αQS, αWSand 18 kinds of β-thal mutations which were common in Chinese population. A total of 454 cases from Guangdong were undergone thal genotype genetic diagnosis. Among the 454 cases, 142 cases were selected to perform the single nucleotide polymorphisms (SNPs) analysis of β- globin gene by denaturing high-performance liquid chromatography (DHPLC)combining the whole gene sequencing.

RESULTS

Of the 454 cases, 438 were diagnosed as thalassemia, including 246 of α-thal, 164 of β-thal and 28 of αβ-thal. In 246 α-thal cases, deletions were the dominant mutations, including 197 cases of αα/--(SEA), 20 of αα/-α(3.7) and 9 of αα/-α(4.2). In 164 β- thal cases, heterozygotes accounted for 92.7% (152/164), the main genotypes were CD41- 42, IVS-II-654, ﹣28 and CD17, and the dual heterozygotes and homozygotes accounted for 4.9% (8/164) and 2.4% (4/164), respectively. The result of β-globin gene screening by DHPLC combining with sequencing was consistent with that of RDB. Moreover, we also found 9 kinds of SNP, in which 2 were unreported, the IVS-I-13 G> A and IVS-II- 310 T>C. In the tested samples, the frequency of 4 kinds SNP was high, among which 3 kinds SNPs-rs713040, rs10768683 and rs1609812 were carried together.

CONCLUSION

The dominant genotypes were αα/--(SEA) in α-thal cases, CD41-42, IVS-II-654, -28 and CD17 in β-thal. The frequency of β-thal heterozygotes, homozygotes and αβ-thal is high. DHPLC combining the whole β-globin gene sequencing can effectively detect the common β-thal mutation and even new mutations or SNPs. In Cantonese, the frequency of SNP rs713040, rs10768683, rs7480526 and rs1609812 of β-globin gene was high, and there may exist genetic linkage between rs713040, rs10768683 and rs1609812.

摘要

目的

了解近年来广东地区人群α、β珠蛋白基因的基因型以及β珠蛋白基因多态性情况,为地中海贫血(地贫)提供有效的基因诊断依据。

方法

采用单管复合PCR技术检测3种缺失型α地贫,反向点杂交(RDB)/PCR技术检测3种非缺失型α地贫——αCS、αQS、αWS以及中国人群常见的18种β地贫突变类型。对454例来自广东地区的样本进行地贫基因分型诊断。其中选取142例样本采用变性高效液相色谱(DHPLC)结合全基因测序技术进行β珠蛋白基因单核苷酸多态性(SNP)分析。

结果

454例样本中,共诊断出地贫438例,其中α地贫246例,β地贫164例,αβ地贫28例。246例α地贫中,缺失型突变占主导,包括αα/--(SEA) 197例,αα/-α(3.7) 20例,αα/-α(4.2) 9例。164例β地贫中,杂合子占92.7%(152/164),主要基因型为CD41-42、IVS-II-654、-28和CD17,双重杂合子和纯合子分别占4.9%(8/164)和2.4%(4/164)。DHPLC结合测序技术对β珠蛋白基因筛查的结果与RDB结果一致。此外,还发现9种SNP,其中2种未见报道,分别为IVS-I-13 G>A和IVS-II-310 T>C。在所检测样本中,4种SNP频率较高,其中3种SNP——rs713040、rs10768683和rs1609812同时出现。

结论

α地贫的主要基因型为αα/--(SEA),β地贫的主要基因型为CD41-42、IVS-II-654、-28和CD17。β地贫杂合子、纯合子及αβ地贫的频率较高。DHPLC结合β珠蛋白全基因测序能有效检测常见β地贫突变甚至新的突变或SNP。在广东地区人群中,β珠蛋白基因SNP rs713040、rs10768683、rs7480526和rs1609812频率较高,且rs713040、rs10768683和rs1609812之间可能存在基因连锁关系。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验