Xu Yunping, Hu Qingsong, Liu Zehuan, Shen Yang, Liu Xiaoyi, Lin Bin, Wu Yuping, Chen Shangwu, Xu Anlong
The Key laboratory of Genetic Engineering of MOE, State Key Laboratory of Biocontrol, Department of Biochemistry, College of Life Sciences, Sun Yat-Sen (Zhongshan) University, Guangzhou, 510275, PR China.
Immunogenetics. 2005 Aug;57(7):465-78. doi: 10.1007/s00251-005-0017-x. Epub 2005 Sep 29.
Sequence polymorphism in the transcriptional regulatory region extending to intron1 (DQRRI1) of HLA-DQB1 gene, and their haplotypic distributions were investigated in southern Chinese populations. We cloned and sequenced a 1.1-kb segment containing the transcriptional regulatory region, exon1, and partial intron1 of HLA-DQB1 gene of 37 individuals from nine different ethnic groups in southern China. A high-density map of 162 polymorphisms, including 152 single nucleotide polymorphisms (SNPs) and 10 insertion-deletion polymorphisms, was revealed. By comparing these data with SNPs deposited in dbSNP database in National Center for Biotechnology Information and polymorphisms that have been reported, 66 polymorphisms were firstly reported. A total of 16 different haplotypes were detected based on these 162 polymorphisms. The distribution of 16 alleles of DQRRI1 as well as their linkage with DQB1 exon2 alleles was also investigated based on the population study and phylogenetic analysis. Tight linkage between these two regions were discovered, as each of DQB102, DQB103, DQB104, DQB105, and DQB1*06 alleles was seen to be linked with specific DQRRI1 allele. Our study showed different pattern of transcriptional regulatory region, exon1, and intron1 of different DQB1 alleles.
我们对中国南方人群中延伸至HLA - DQB1基因内含子1(DQRRI1)的转录调控区域的序列多态性及其单倍型分布进行了研究。我们克隆并测序了来自中国南方九个不同民族的37个个体的一段1.1 kb片段,该片段包含HLA - DQB1基因的转录调控区域、外显子1和部分内含子1。结果揭示了一个由162个多态性组成的高密度图谱,其中包括152个单核苷酸多态性(SNP)和10个插入 - 缺失多态性。通过将这些数据与美国国立生物技术信息中心dbSNP数据库中存储的SNP以及已报道的多态性进行比较,首次报道了66个多态性。基于这162个多态性共检测到16种不同的单倍型。基于群体研究和系统发育分析,我们还研究了DQRRI1的16个等位基因的分布及其与DQB1外显子2等位基因的连锁情况。发现这两个区域之间存在紧密连锁,因为观察到DQB102、DQB103、DQB104、DQB105和DQB1*06等位基因中的每一个都与特定的DQRRI1等位基因连锁。我们的研究显示了不同DQB1等位基因的转录调控区域、外显子1和内含子1的不同模式。