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非洲黑腹果蝇群体中Adh和P6基因的分子变异及其与染色体倒位的关系。

Molecular variation of Adh and P6 genes in an African population of Drosophila melanogaster and its relation to chromosomal inversions.

作者信息

Bénassi V, Aulard S, Mazeau S, Veuille M

机构信息

Laboratoire de Biologie et Génétique Evolutives, Centre National de la Recherche Scientifique, Gif-sur-Yvette, France.

出版信息

Genetics. 1993 Jul;134(3):789-99. doi: 10.1093/genetics/134.3.789.

Abstract

Four-cutter molecular polymorphism of Adh and P6, and chromosome inversion polymorphism of chromosome II were investigated in 95 isogenic lines of an Ivory Coast population of Drosophila melanogaster, a species assumed to have recently spread throughout the world from a West African origin. The P6 gene showed little linkage disequilibrium with the In(2L)t inversion, although it is located within this inversion. This suggests that the inversion and the P6 locus have extensively exchanged genetic information through either double crossover or gene conversion. Allozymic variation in ADH was in linkage disequilibrium with In(2L)t and In(2R)NS inversions. Evidence suggests either that inversion linkage with the Fast allele is selectively maintained, or that this allele only recently appeared. Molecular polymorphism at the Adh locus in the Ivory Coast is not higher than in North American populations. New haplotypes specific to the African population were found, some of them connect the "WaS-like" haplotypes found at high frequencies in the United States to the other slow haplotypes. Their relation with In(2L)t supports the hypothesis that WaS recently recombined away from an In(2L)t chromosome which may be the cause of its divergence from the other haplotypes.

摘要

在假定最近从西非起源扩散至全球的黑腹果蝇的95个象牙海岸种群的同基因系中,研究了乙醇脱氢酶(Adh)和P6的四切割分子多态性以及第二号染色体的染色体倒位多态性。尽管P6基因位于In(2L)t倒位内,但它与该倒位几乎没有连锁不平衡。这表明该倒位和P6基因座通过双交换或基因转换广泛地交换了遗传信息。乙醇脱氢酶(ADH)的等位酶变异与In(2L)t和In(2R)NS倒位存在连锁不平衡。有证据表明,要么与快速等位基因的倒位连锁是被选择性维持的,要么就是这个等位基因最近才出现。象牙海岸Adh基因座的分子多态性并不高于北美种群。发现了非洲种群特有的新单倍型,其中一些将在美国高频率发现的“WaS样”单倍型与其他慢速单倍型联系起来。它们与In(2L)t的关系支持了这样一种假设,即WaS最近从In(2L)t染色体上重组分离出来,这可能是其与其他单倍型发生分化的原因。

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