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重复序列与小鼠溶菌酶基因的复制及分化

Repetitive sequence involvement in the duplication and divergence of mouse lysozyme genes.

作者信息

Cross M, Renkawitz R

机构信息

Genzentrum, Max-Planck-Institut für Biochemie, Martinsried, FRG.

出版信息

EMBO J. 1990 Apr;9(4):1283-8. doi: 10.1002/j.1460-2075.1990.tb08237.x.

Abstract

Mouse M and P lysozymes are the products of separate genes, are specifically expressed in separate tissues, and are adapted to different functions. The lysozyme genes have assumed these markedly different characteristics following their generation by gene duplication 30-50 million years ago. The discovery of the lysozyme P gene only 5 kb upstream from the M gene in tandem repeat has enabled an investigation of the molecular basis of their duplication and subsequent divergence. The duplication is shown to have involved recombination between two B2 repeat sequences flanking the original gene. The resulting downstream copy has retained the myeloid specificity of expression along with just 1.7 kb of upstream sequences, while the upstream copy is inactive in macrophages and has become expressed instead in the small intestine. Although multiple gene conversion events have served to maintain a generally high homology between the genes, certain regions have been found to be specific for either one of the gene pair: two repetitive sequences peculiar to the P region may serve to protect the coding regions from gene conversion, while sequences unique to the M gene may be more directly involved in differential regulation.

摘要

小鼠M型和P型溶菌酶是不同基因的产物,在不同组织中特异性表达,并适应不同功能。溶菌酶基因在3000万至5000万年前通过基因复制产生后,呈现出这些明显不同的特征。在串联重复中,溶菌酶P基因在距M基因仅5 kb的上游被发现,这使得对它们复制及随后分化的分子基础进行研究成为可能。研究表明,复制涉及原始基因两侧两个B2重复序列之间的重组。产生的下游拷贝保留了髓系特异性表达以及仅1.7 kb的上游序列,而上游拷贝在巨噬细胞中无活性,转而在小肠中表达。尽管多个基因转换事件有助于维持基因之间普遍较高的同源性,但已发现某些区域对基因对中的任何一个具有特异性:P区域特有的两个重复序列可能有助于保护编码区域免受基因转换,而M基因特有的序列可能更直接参与差异调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1984/551806/15baf0d95de9/emboj00231-0305-a.jpg

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