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生殖系V基因的起源与维持。

Origin and maintenance of germ-line V genes.

作者信息

Rothenfluh H S, Steele E J

机构信息

Department of Biological Sciences, University of Wollongong, New South Wales, Australia.

出版信息

Immunol Cell Biol. 1993 Jun;71 ( Pt 3):227-32. doi: 10.1038/icb.1993.26.

Abstract

The distribution of nucleotide variability within the upstream of germ-line VH186.2-related variable genes was studied. The data in this report of work in progress indicate non-random selection for variability in the second antigen-contact or complementarity-determining region (CDR2) for 12 such genes isolated using the polymerase chain reaction (PCR) technique from genomic C57BL/6 mouse liver DNA. The translated protein sequences of these and three additional previously published genes also display a pronounced Wu-Kabat peak of amino acid variability in CDR2. In the CDR1 and CDR2 regions of this set of related germ-line genes, there are few [corrected] silent nucleotide changes, and most amino acid replacements (or non-synonymous changes) are non-conservative. In contrast, there is selection against amino acid replacement in the framework regions (FW), as indicated by the significant number of silent (or synonymous) mutational changes from the VH186.2 reference sequence. This is surprisingly similar to the Wu-Kabat variability patterns observed in somatically mutated immune response antibodies. These data could imply similar diversification mechanisms acting on B cell-expressed V genes in the soma (i.e. in a germinal centre) and in the germ-line DNA of male and/or female germ cells. While always possible, we consider this unlikely. Similarly, we consider as unlikely an explanation based on a classical Darwinian model involving simple stepwise whole animal selection prior to reproduction for each VH and VL gene now phylogenetically stored in the V segment arrays of the genomic DNA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对种系VH186.2相关可变基因上游的核苷酸变异性分布进行了研究。本进展报告中的数据表明,使用聚合酶链反应(PCR)技术从基因组C57BL/6小鼠肝脏DNA中分离出的12个此类基因,在第二个抗原接触或互补决定区(CDR2)的变异性存在非随机选择。这些基因以及另外三个先前发表基因的翻译蛋白质序列在CDR2中也显示出明显的氨基酸变异性的吴-卡巴特峰。在这组相关种系基因的CDR1和CDR2区域,几乎没有[校正后]沉默核苷酸变化,并且大多数氨基酸替换(或非同义变化)是非保守的。相比之下,如从VH186.2参考序列中大量的沉默(或同义)突变变化所示,在框架区(FW)存在对氨基酸替换的选择抑制。这与在体细胞突变的免疫应答抗体中观察到的吴-卡巴特变异性模式惊人地相似。这些数据可能意味着在体细胞(即生发中心)以及雄性和/或雌性生殖细胞的种系DNA中,作用于B细胞表达的V基因的多样化机制相似。虽然总是有可能,但我们认为这种可能性不大。同样,我们认为基于经典达尔文模型的解释也不太可能,该模型涉及在每个VH和VL基因现在系统发育地存储在基因组DNA的V区段阵列中之前,在繁殖前对整个动物进行简单的逐步选择。(摘要截短至250字)

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