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果蝇种内核DNA变异

Intraspecific nuclear DNA variation in Drosophila.

作者信息

Moriyama E N, Powell J R

机构信息

Department of Biology, Yale University, New Haven, Connecticut 06520-8104, USA.

出版信息

Mol Biol Evol. 1996 Jan;13(1):261-77. doi: 10.1093/oxfordjournals.molbev.a025563.

Abstract

We have summarized and analyzed all available nuclear DNA sequence polymorphism studies for three species of Drosophila, D. melanogaster (24 loci), D. simulans (12 loci), and D. pseudoobscura (5 loci). Our major findings are: (1) The average nucleotide heterozygosity ranges from about 0.4% to 2% depending upon species and function of the region, i.e., coding or noncoding. (2) Compared to D. simulans and D. pseudoobscura (which are about equally variable), D. melanogaster displays a low degree of DNA polymorphism. (3) Noncoding introns and 3' and 5' flanking DNA shows less polymorphism than silent sites within coding DNA. (4) X-linked genes are less variable than autosomal genes. (5) Transition (Ts) and transversion (Tv) polymorphisms are about equally frequent in non-coding DNA and at fourfold degenerate sites in coding DNA while Ts polymorphisms outnumber Tv polymorphisms by about 2:1 in total coding DNA. The increased Ts polymorphism in coding regions is likely due to the structure of the genetic code: silent changes are more often Ts's than are replacement substitutions. (6) The proportion of replacement polymorphisms is significantly higher in D. melanogaster than in D. simulans. (7) The level of variation in coding DNA and the adjacent noncoding DNA is significantly correlated indicating regional effects, most notably recombination. (8) Surprisingly, the level of polymorphism at silent coding sites in D. melanogaster is positively correlated with degree of codon usage bias. (9) Three proposed tests of the neutral theory of DNA polymorphisms have been performed on the data: Tajima's test, the HKA test, and the McDonald-Kreitman test. About half of the loci fail to conform to the expectations of neutral theory by one of the tests. We conclude that many variables are affecting levels of DNA polymorphism in Drosophila, from properties of nucleotides to population history and, perhaps, mating structure. No simple, all encompassing explanation satisfactorily accounts for the data.

摘要

我们总结并分析了针对三种果蝇(黑腹果蝇(24个基因座)、拟暗果蝇(12个基因座)和伪暗果蝇(5个基因座))的所有现有核DNA序列多态性研究。我们的主要发现如下:(1)平均核苷酸杂合度根据物种和区域功能(即编码或非编码)的不同,在约0.4%至2%的范围内变化。(2)与拟暗果蝇和伪暗果蝇(二者的变异性大致相同)相比,黑腹果蝇的DNA多态性程度较低。(3)非编码内含子以及3'和5'侧翼DNA的多态性低于编码DNA中的沉默位点。(4)X连锁基因的变异性低于常染色体基因。(5)在非编码DNA以及编码DNA的四倍简并位点处,转换(Ts)和颠换(Tv)多态性的频率大致相同,而在整个编码DNA中,Ts多态性的数量比Tv多态性约多2:1。编码区域中Ts多态性的增加可能归因于遗传密码的结构:沉默变化中Ts出现的频率比替换替换更高。(6)黑腹果蝇中替换多态性的比例显著高于拟暗果蝇。(7)编码DNA及其相邻非编码DNA中的变异水平显著相关,表明存在区域效应,最显著的是重组。(8)令人惊讶的是,黑腹果蝇中沉默编码位点的多态性水平与密码子使用偏好程度呈正相关。(9)已对这些数据进行了三种针对DNA多态性中性理论的提议测试: Tajima测试、HKA测试和McDonald-Kreitman测试。约一半的基因座未能通过其中一项测试符合中性理论的预期。我们得出结论,许多变量正在影响果蝇中DNA多态性的水平,从核苷酸特性到种群历史,或许还有交配结构。没有一个简单、全面的解释能令人满意地解释这些数据。

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