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α位点性别决定基因的单倍剂量不足限制了……中的基因组扩展。

Haploinsufficiency of the sex-determining genes at α restricts genome expansion in .

作者信息

Oya Kazumasa, Matsuura Akira

机构信息

Department of Biology, Graduate School of Science and Engineering, Chiba University, 1-33 Yayoi-chou, Inage-ku, Chiba 263-8522, Japan.

Department of Biology, Graduate School of Science, Chiba University, 1-33 Yayoi-chou, Inage-ku, Chiba 263-8522, Japan.

出版信息

iScience. 2022 Jul 19;25(8):104783. doi: 10.1016/j.isci.2022.104783. eCollection 2022 Aug 19.

Abstract

In , mating type of haploid cells is determined by the presence or absence of the α idiotype containing and , which encode the transcription factors. These proteins are characterized by rapid turnover, but the physiological relevance of this property remains unclear. Here, we show a direct link between their intracellular levels and sexual stability. Polyploid cells with fewer α copies had unstable sexual phenotypes, causing morphological changes and an increase in cell death; these effects were mediated by hyperactivation of the mating pheromone response pathway. Thus, the and genes are haploinsufficient genes, and the reduction in their product levels causes sex fluctuation. Chromosome III harboring the mating type locus is the most prone to loss in diploids. We propose that the haploinsufficiency of α compensates for the drop-out prone nature of chromosome III, thereby suppressing speciation through increased genome size via polyploidization.

摘要

在[具体物种或研究背景未提及]中,单倍体细胞的交配型由含有[具体基因名称1]和[具体基因名称2]的α独特型的存在与否决定,这两个基因编码转录因子。这些蛋白质的特点是周转迅速,但其这一特性的生理相关性仍不清楚。在这里,我们展示了它们的细胞内水平与性稳定性之间的直接联系。α拷贝数较少的多倍体细胞具有不稳定的性表型,导致形态变化和细胞死亡增加;这些效应是由交配信息素反应途径的过度激活介导的。因此,[具体基因名称1]和[具体基因名称2]基因是单倍剂量不足基因,其产物水平的降低会导致性别波动。携带交配型位点的第三条染色体在二倍体中最容易丢失。我们提出,α的单倍剂量不足补偿了第三条染色体易于缺失的特性,从而通过多倍化增加基因组大小来抑制物种形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf9/9379577/619dd0120915/fx1.jpg

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