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巴氏果蝇的进化史。 XXI. 多种不育因子对巴氏果蝇和科普费尔果蝇杂交种精子发生的累积作用。

The evolutionary history of Drosophila buzzatii. XXI. Cumulative action of multiple sterility factors on spermatogenesis in hybrids of D. buzzatii and D. koepferae.

作者信息

Naveira H, Fondevila A

机构信息

Departamento de Fundamental, Facultad de Biuologia, Universidad de Santiago de Compostela, Spain.

出版信息

Heredity (Edinb). 1991 Aug;67 ( Pt 1):57-72. doi: 10.1038/hdy.1991.65.

Abstract

The genetic basis of sterility in male hybrids of Drosophila buzzatii and D. koepferae has been investigated by assessment of the effects on spermatogenesis of substituting separate chromosome segments of the recipient species with the homologous material from the donor species, either in heterozygous (autosomes) or hemizygous (X chromosome) condition, after successive backcrossing of hybrid females to either parental species. Introgressed segments were identified by the characteristic asynapsis of the polytene chromosomes in their heterospecific regions. Except for one case, the introgression of chromosome segments either from autosome 3, 4, or 5 brings about sterility only when the introgressed segment exceeds a minimum size (threshold size). Segments of equal size frequently produce similar abnormalities, whose severity increases with the size of the introgressed segment. Apparently, throughout these autosomes of D. buzzatii and D. koepferae there are many non-allelic, minor sterility genes, whose individual segregation cannot be recognized phenotypically, and which act cumulatively on the same characteristics of spermatogenesis, each contributing a small effect to the phenotype. Accordingly, these genes should be considered as polygenes, and the type of sterility they bring about should be properly designated polygenic sterility.

摘要

通过评估在杂种雌性与任一亲本物种连续回交后,将受体物种的单独染色体片段用供体物种的同源物质进行替代(处于杂合状态(常染色体)或半合子状态(X染色体))对精子发生的影响,研究了巴氏果蝇和科氏果蝇雄性杂种不育的遗传基础。渐渗片段通过其异源特异性区域中多线染色体的特征性不联会来鉴定。除了一种情况外,来自常染色体3、4或5的染色体片段渐渗仅在渐渗片段超过最小大小(阈值大小)时才会导致不育。等大小的片段经常产生相似的异常,其严重程度随着渐渗片段的大小而增加。显然,在巴氏果蝇和科氏果蝇的这些常染色体中存在许多非等位的、微小不育基因,其个体分离无法通过表型识别,并且它们对精子发生的相同特征起累积作用,每个基因对表型的贡献很小。因此,这些基因应被视为多基因,它们导致的不育类型应正确地称为多基因不育。

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