局部DNA影响人类α -干扰素基因家族替代模式的证据。

G B Golding, B W Glickman
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引用次数: 11

摘要

如果序列足够广泛,可以提供可靠的数据,基因的进化史可以用来检查自发突变的模式。许多人类α -干扰素基因已被测序,它们形成了一个大的多基因家族,包括一些假基因。重建了15个人类干扰素序列的系统发育历史,并利用最大简约法推断了它们的祖先序列。这个进化史提供了在人类最近的进化中发生的超过738个自发突变的记录。在这些突变中,分析了超过267个碱基置换和缺失插入事件,以确定附近DNA序列的可能影响。许多替换发生在相同碱基的长链末端,一些二核苷酸对可能比其他二核苷酸对更频繁地突变。由于局部DNA序列的模板化与原核突变有关,因此还检查了这些序列附近的重复序列,这些重复序列包括取代的核苷酸,因此可能具有模板化替代的能力。大多数被检查的序列改变要么有类似的直接重复,要么附近有回文。通常这样的模板可以解释同时发生的多个突变。这些结果表明,序列导向事件可能偶尔发生在真核生物中,邻近的DNA序列可以以几种不同的方式影响突变的发生和类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence for local DNA influences on patterns of substitutions in the human alpha-interferon gene family.

The evolutionary history of genes can be used to examine patterns of spontaneous mutation if the sequences are sufficiently extensive to provide reliable data. Many human alpha-interferon genes have been sequenced and they form a large multigene family including several pseudogenes. A phylogenetic history for 15 human interferon sequences was reconstructed and their ancestral sequences inferred using a maximum parsimony method. This evolutionary history provided a record of more than 738 spontaneous mutations that have occurred in man's recent evolution. Of these mutations, more than 267 base substitution and deletion-insertion events were analyzed to determine the possible effects of nearby DNA sequences. Many substitutions occur at the end of long runs of identical bases and some dinucleotide pairs may mutate more often than others. Because templating by local DNA sequences has been implicated in prokaryotic mutation, the sequences were also examined for nearby repeats that include the substituted nucleotide and hence are potentially capable of templating the substitution. The majority of sequence alterations examined have either a similar direct repeat or palindrome nearby. Often such templates can account for simultaneous multiple mutations. These results suggest that sequence-directed events may occur occasionally in eukaryotes and that neighbouring DNA sequences can influence both the occurrence and types of mutations in several different ways.

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