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一种新型HLA - F等位基因 - HLA - F*010102的鉴定。

Identification of a novel HLA-F allele - HLA-F*010102.

作者信息

He X, Xu L, Liu Y, Zeng Y

机构信息

Key Laboratory of Ministry of Education for Tissue Transplantation and Immunology, Guangzhou, People's Republic of China.

出版信息

Tissue Antigens. 2004 Feb;63(2):181-3. doi: 10.1111/j.1399-0039.2004.00145.x.

Abstract

We describe herein the identification of HLA-F010102 by cloning the full-length coding sequence with reverse-transcription polymerase chain reaction (RT-PCR). This new allele was found in two Han Chinese individuals in the course of cloning major histocompatibility complex class Ib (MHC Ib) cDNA. It was identical to HLA-F010101 except for a single-nucleotide substitution in codon -1 (GCG --> GCA). This nucleotide change represents a synonymous mutation, as both triplets code for an alanine. The cDNA of this allele was 48 bp shorter than HLA-F*010101 due to splicing out exon 7. Analysis of the deduced amino acid sequence revealed that the product of this new allele had the identical extracellular domain and transmembrane region but had a shorter cytoplasmic tail.

摘要

我们在此描述了通过逆转录聚合酶链反应(RT-PCR)克隆全长编码序列来鉴定HLA-F010102。在克隆主要组织相容性复合体I类b(MHC Ib)cDNA的过程中,在两名汉族个体中发现了这个新等位基因。它与HLA-F010101相同,只是密码子-1处有一个单核苷酸替换(GCG --> GCA)。这种核苷酸变化代表同义突变,因为两个三联体都编码丙氨酸。由于外显子7的剪接,这个等位基因的cDNA比HLA-F*010101短48 bp。对推导的氨基酸序列分析表明,这个新等位基因的产物具有相同的细胞外结构域和跨膜区域,但细胞质尾巴较短。

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