Zhen Jianxin, Zhang Guobin, Yu Qiong, He Liumei, Xu Yunping, Zou Hongyan, Deng Zhihui
Shenzhen Blood Center, Shenzhen, Guangdong 518035, China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):21-25. doi: 10.3760/cma.j.issn.1003-9406.2017.01.005.
To study genetic polymorphisms of the KIR2DS4 gene among ethnic Hans from southern China.
Genomic DNA was isolated from 306 unrelated individuals and amplified with KIR2DS4-specific PCR primers. KIR2DS4-positive samples were genotyped for the entire coding sequence by sequencing-based typing (SBT). Assignment of allelic genotypes was accomplished by using Assign 3.5 software. For samples with inconclusive SBT results, RT-PCR products covering the entire coding sequence of the KIR2DS4 gene were subjected to cloning and haplotype sequencing.
Among all tested samples, 297 were demonstrated to have carried the KIR2DS4 framework gene. For KIR2DS4-positive samples subjected to SBT for the entire coding sequences, no background was observed with the obtained sequences. Three of the seven identified alleles were of novel types, which were officially named by the KIR subcommittee of the World Health Organization Nomenclature Committee for Factors of HLA System. The observed frequencies for the 7 alleles were KIR2DS4*00101 (78.8%), *003 (10.5%), *004 (16.0%), *010 (23.2%), *017 (0.3%), 00105 (0.3%) and 018 (0.7%), respectively. Allele KIR2DS4007 was not found. The overall frequency for normal cell-surface expression KIR2DS4 alleles including 2DS400101, *017 and 00105 was 79.4%, and that for non cell-surface expression alleles including 2DS4003, *004, *010 and *018 was 50.4%. The ratio between the two was 1.6:1.
The present study has elucidated the allelic diversity of KIR2DS4 among ethnic Hans from southern China, which may provide valuable data for transplantation as well as studies on KIR-associated disease and evolution.
研究中国南方汉族人群中KIR2DS4基因的遗传多态性。
从306名无亲缘关系的个体中分离基因组DNA,并用KIR2DS4特异性PCR引物进行扩增。对KIR2DS4阳性样本通过基于测序的分型(SBT)对整个编码序列进行基因分型。使用Assign 3.5软件完成等位基因基因型的指定。对于SBT结果不确定的样本,对覆盖KIR2DS4基因整个编码序列的RT-PCR产物进行克隆和单倍型测序。
在所有检测样本中,有297个被证明携带KIR2DS4框架基因。对KIR2DS4阳性样本的整个编码序列进行SBT时,所获得的序列未观察到背景。鉴定出的7个等位基因中有3个是新型的,已由世界卫生组织HLA系统因子命名委员会的KIR小组委员会正式命名。7个等位基因的观察频率分别为KIR2DS4*00101(78.8%)、*003(10.5%)、004(16.0%)、010(23.2%)、017(0.3%)、00105(0.3%)和018(0.7%)。未发现等位基因KIR2DS4007。包括2DS400101、017和00105在内的正常细胞表面表达KIR2DS4等位基因的总体频率为79.4%,包括2DS4003、*004、010和018在内的非细胞表面表达等位基因的总体频率为50.4%。两者之比为1.6:1。
本研究阐明了中国南方汉族人群中KIR2DS4的等位基因多样性,这可能为移植以及KIR相关疾病和进化的研究提供有价值的数据。