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杀伤细胞免疫球蛋白样受体基因多样性、KIR2DL1和KIR2DS1的研究

Investigation of killer cell immunoglobulin-like receptor gene diversity, KIR2DL1 and KIR2DS1.

作者信息

Meenagh A, Gonzalez A, Sleator C, McQuaid S, Middleton D

机构信息

Northern Ireland Regional Histocompatibility and Immunogenetics Laboratory, City Hospital, Belfast, UK.

出版信息

Tissue Antigens. 2008 Oct;72(4):383-91. doi: 10.1111/j.1399-0039.2008.01093.x. Epub 2008 Jul 15.

Abstract

Polymorphism in the alleles of the killer cell immunoglobulin-like receptor 2DL1 and 2DS1 genes has been investigated by the development of polymerase chain reaction-sequence-specific oligonucleotide probing systems. The methods have been applied to 77 Northern Irish families, establishing allele frequencies from the unrelated parents. Additionally, cell line DNA from individuals and CEPH families of the 13th International Histocompatibility Workshop panel were investigated. Eight of the reported KIR2DL1 alleles and only the KIR2DS1002 allele were identified in the groups studied. Two individuals were positive for three alleles of KIR2DL1, and a putative variant of KIR2DL1001 was observed. Results also indicated an inherited KIR2DL1/2DS1 splice variant present in a haplotype with several core loci absent, in two families.

摘要

通过聚合酶链反应-序列特异性寡核苷酸探针系统的开发,对杀伤细胞免疫球蛋白样受体2DL1和2DS1基因的等位基因多态性进行了研究。这些方法已应用于77个北爱尔兰家庭,从不相关的父母中确定等位基因频率。此外,还对第13届国际组织相容性研讨会小组的个体和CEPH家庭的细胞系DNA进行了研究。在所研究的群体中鉴定出了8个已报道的KIR2DL1等位基因,且仅鉴定出了KIR2DS1002等位基因。两名个体的KIR2DL1三个等位基因呈阳性,并观察到KIR2DL1001的一个推定变体。结果还表明,在两个家庭中,存在一种遗传性的KIR2DL1/2DS1剪接变体,该变体存在于一个单倍型中,其中几个核心基因座缺失。

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