Suppr超能文献

一个基因家族中被认可的突变:重复DNA的进化多样化

Accepted mutations in a gene family: evolutionary diversification of duplicated DNA.

作者信息

Jones C W, Kafatos F C

出版信息

J Mol Evol. 1982;19(1):87-103. doi: 10.1007/BF02100227.

Abstract

We report and compare the DNA sequences of 14 silkmoth (Antheraea polyphemus) chorion genes, derived from either cDNA or chromosomal DNA clones. Seven of these genes are members of the A multigene family, and seven are members of the B family. Where available, the previously reported (Jones and Kafatos 1980) intronic and extragenic flanking DNA sequences are also considered. Closely related sequences are compared, revealing the types of spontaneous mutations that were fixed during paralogous evolution. Segmental mutations (i.e. mutations other than substitutions) are nearly always interpretable as small duplications or deletions, related to small direct repeats. Segmental mutations are strongly constrained in the coding regions, although they do occur. Nucleotide substitutions also appear to be under selective constraints: relatively few substitutions leading to amino acid replacements are accepted, silent substitutions leading to some codons (especially purine-terminated ones) are disfavored, and different compositional biases are maintained in different parts of the sequences. Other sequence differences can be interpreted as indicative of neutral drift, including most differences in non-coding regions and most T/C transitions in third-base positions. In the non-coding regions, which are thought to be only loosely constrained by selection, transitions are observed more frequently than might be expected: they account for 52% of all substitutions, and they appear to be favored two to threefold over transversions when allowance is made for the skewed base composition of these regions.

摘要

我们报告并比较了14个家蚕(多音天蚕)绒毛膜基因的DNA序列,这些序列来源于cDNA或染色体DNA克隆。其中7个基因是A多基因家族的成员,7个是B家族的成员。在有可用信息的情况下,还考虑了先前报道的(琼斯和卡法托斯,1980年)内含子和基因外侧翼DNA序列。对密切相关的序列进行比较,揭示了在旁系同源进化过程中固定下来的自发突变类型。片段突变(即取代以外的突变)几乎总是可以解释为与小的直接重复相关的小的重复或缺失。片段突变在编码区受到强烈限制,尽管它们确实会发生。核苷酸取代似乎也受到选择限制:导致氨基酸替换的取代相对较少被接受,导致某些密码子(特别是嘌呤终止的密码子)的沉默取代不受欢迎,并且在序列的不同部分保持不同的组成偏差。其他序列差异可以解释为中性漂移的指示,包括非编码区的大多数差异和第三位碱基的大多数T/C转换。在被认为仅受到选择的松散限制的非编码区,转换的观察频率比预期的要高:它们占所有取代的52%,并且当考虑到这些区域的碱基组成偏斜时,它们似乎比颠换更受青睐两到三倍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验