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小鼠I-Aα的结构、调控多态性和等位基因高变区

Structure, regulatory polymorphisms, and allelic hypervariability regions in murine I-A alpha.

作者信息

McDevitt H O, Mathis D J, Benoist C, Kanter M R, Williams V E

出版信息

Fed Proc. 1984 Dec;43(15):3021-4.

PMID:6437873
Abstract

Class II major histocompatibility complex (MHC) molecules, the Ia antigens, are intimately involved in regulating the intensity and specificity of the cellular and humoral responses to T cell-dependent antigens. One approach to understanding the mechanism of this regulation is to analyze the structure and allelic polymorphism of Ia molecules. In addition there are regulatory polymorphisms in the expression of the I-E alpha and I-E beta class II MHC polypeptide chains. Analysis of the cDNA sequence indicates that I-A and I-E alpha chains are similar with short stretches of homology and other regions of nonhomology. Analysis of Northern blots of mRNA indicates that at least three separate types of regulatory polymorphisms result in failure of expression of I-E alpha. Comparison of allelic sequences of six alleles of the I-A alpha chain shows that almost all of the allelic polymorphism is in the first domain and that within the first domain it is clustered in three allelic hypervariable regions within the first domain of I-A alpha. The structural and functional implications of these findings are discussed.

摘要

II类主要组织相容性复合体(MHC)分子,即Ia抗原,密切参与调节针对T细胞依赖性抗原的细胞和体液免疫反应的强度和特异性。理解这种调节机制的一种方法是分析Ia分子的结构和等位基因多态性。此外,II类MHC I-Eα和I-Eβ多肽链的表达存在调节性多态性。对cDNA序列的分析表明,I-A和I-Eα链相似,有短的同源片段和其他非同源区域。对mRNA的Northern印迹分析表明,至少三种不同类型的调节性多态性导致I-Eα表达失败。对I-Aα链六个等位基因的等位基因序列比较表明,几乎所有的等位基因多态性都在第一个结构域,并且在第一个结构域内,它聚集在I-Aα第一个结构域内的三个等位基因高变区。讨论了这些发现的结构和功能意义。

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