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蛋白质复合物紊乱引起的蛋白毒性是酵母杂种不育的基础。

Proteotoxicity caused by perturbed protein complexes underlies hybrid incompatibility in yeast.

机构信息

Institute of Molecular Biology, Academia Sinica, Taipei, 11529, Taiwan.

Division of Biological and Life Sciences, School of Arts and Sciences, Ahmedabad University, Ahmedabad, 380009, India.

出版信息

Nat Commun. 2022 Jul 29;13(1):4394. doi: 10.1038/s41467-022-32107-4.

Abstract

Dobzhansky-Muller incompatibilities represent a major driver of reproductive isolation between species. They are caused when interacting components encoded by alleles from different species cannot function properly when mixed. At incipient stages of speciation, complex incompatibilities involving multiple genetic loci with weak effects are frequently observed, but the underlying mechanisms remain elusive. Here we show perturbed proteostasis leading to compromised mitosis and meiosis in Saccharomyces cerevisiae hybrid lines carrying one or two chromosomes from Saccharomyces bayanus var. uvarum. Levels of proteotoxicity are correlated with the number of protein complexes on replaced chromosomes. Proteomic approaches reveal that multi-protein complexes with subunits encoded by replaced chromosomes tend to be unstable. Furthermore, hybrid defects can be alleviated or aggravated, respectively, by up- or down-regulating the ubiquitin-proteasomal degradation machinery, suggesting that destabilized complex subunits overburden the proteostasis machinery and compromise hybrid fitness. Our findings reveal the general role of impaired protein complex assembly in complex incompatibilities.

摘要

多倍体-穆勒不兼容性是物种间生殖隔离的主要驱动因素。当来自不同物种的等位基因编码的相互作用成分混合时不能正常发挥作用时,就会产生这种不兼容性。在物种形成的初期阶段,经常观察到涉及多个遗传位点且作用较弱的复杂不兼容性,但潜在的机制仍难以捉摸。在这里,我们展示了在携带一个或两个来自酿酒酵母巴氏亚种 var.uvarum 染色体的酿酒酵母杂交系中,失调的蛋白质稳态导致有丝分裂和减数分裂受损。蛋白质毒性水平与替换染色体上的蛋白质复合物数量相关。蛋白质组学方法表明,由替换染色体编码的多蛋白复合物往往不稳定。此外,通过上调或下调泛素-蛋白酶体降解机制,分别可以减轻或加重杂种缺陷,这表明不稳定的复合物亚基会使蛋白质稳态机制负担过重,并影响杂种的适应性。我们的研究结果揭示了受损的蛋白质复合物组装在复杂不兼容性中的普遍作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9847/9338014/cdc59e4ff44c/41467_2022_32107_Fig1_HTML.jpg

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