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局部DNA对人类α-干扰素基因家族中替换模式影响的证据。

Evidence for local DNA influences on patterns of substitutions in the human alpha-interferon gene family.

作者信息

Golding G B, Glickman B W

出版信息

Can J Genet Cytol. 1986 Aug;28(4):483-96. doi: 10.1139/g86-072.

DOI:10.1139/g86-072
PMID:3756607
Abstract

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.

摘要

如果基因序列足够广泛以提供可靠数据,那么基因的进化史可用于研究自发突变模式。许多人类α-干扰素基因已被测序,它们形成了一个包括多个假基因的大型多基因家族。利用最大简约法重建了15个人类干扰素序列的系统发育史,并推断出它们的祖先序列。这一进化史记录了人类近期进化过程中发生的738多个自发突变。在这些突变中,分析了超过267个碱基替换和缺失-插入事件,以确定附近DNA序列可能产生的影响。许多替换发生在相同碱基的长串末端,一些二核苷酸对可能比其他的更容易发生突变。由于原核生物突变涉及局部DNA序列的模板作用,因此还检查了这些序列附近的重复序列,这些重复序列包含被替换的核苷酸,因此可能能够为替换提供模板。所检查的大多数序列改变在附近都有类似的直接重复序列或回文序列。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在真核生物中发生,并且相邻的DNA序列可以通过几种不同方式影响突变的发生和类型。

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Evidence for local DNA influences on patterns of substitutions in the human alpha-interferon gene family.局部DNA对人类α-干扰素基因家族中替换模式影响的证据。
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引用本文的文献

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Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes.相邻核苷酸对人类基因种系单碱基对替换率的影响。
Am J Hum Genet. 1998 Aug;63(2):474-88. doi: 10.1086/301965.
2
Substitution rate variation among sites in hypervariable region 1 of human mitochondrial DNA.人类线粒体DNA高变区1中各位点间的替换率变异
J Mol Evol. 1993 Dec;37(6):613-23. doi: 10.1007/BF00182747.
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Synonymous substitutions are clustered in enterobacterial genes.同义替换集中在肠道细菌基因中。
J Mol Evol. 1994 Nov;39(5):448-51. doi: 10.1007/BF00173413.
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The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions.导致人类遗传疾病的单碱基对替换的突变谱:模式与预测。
Hum Genet. 1990 Jun;85(1):55-74. doi: 10.1007/BF00276326.
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Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat.由二核苷酸重复序列缺失引起的常染色体隐性慢性肉芽肿病。
Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2753-7. doi: 10.1073/pnas.88.7.2753.