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利用HLA突变细胞系将人类MHC连锁补体基因定位在HLA - B和HLA - DR之间。

Localization of the human MHC-linked complement genes between HLA-B and HLA-DR by using HLA mutant cell lines.

作者信息

Whitehead A S, Colten H R, Chang C C, Demars R

出版信息

J Immunol. 1985 Jan;134(1):641-3.

PMID:3917284
Abstract

A C4 cDNA clone has been used to localize the C4 genes within the human major histocompatibility complex (MHC). The clone, pC4AL1, detects a DNA polymorphism of the C4 genes in Southern blot hybridization experiments and established the genotype of a lymphoblastoid cell line, LCL 721, as heterozygous for the C4 DNA patterns. Subclones of LCL 721 that had gamma-ray-induced lesions of the MHC were analyzed with pC4AL1. Loss or retention of chromosome-specific C4 DNA patterns relative to the loss or retention of other MHC genes on the same chromosome was assessed. This permitted the mapping of the C4 genes, and the other MHC-linked complement genes, between the HLA-DR and HLA-B loci.

摘要

一个C4 cDNA克隆已被用于将C4基因定位在人类主要组织相容性复合体(MHC)内。该克隆pC4AL1在Southern印迹杂交实验中检测到C4基因的DNA多态性,并确定了淋巴母细胞系LCL 721的基因型为C4 DNA模式杂合子。用pC4AL1分析了具有γ射线诱导的MHC损伤的LCL 721亚克隆。评估了相对于同一条染色体上其他MHC基因的丢失或保留,染色体特异性C4 DNA模式的丢失或保留情况。这使得能够将C4基因以及其他与MHC连锁的补体基因定位在HLA-DR和HLA-B基因座之间。

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