Saccharomyces cerevisiae Mub1, a substrate adaptor of E3 ubiquitin ligase Ubr2, modulates sensitivity to cell wall stressors through multiple transcription factors.

Nada Šupljika, Antonia Paić, Ana Novačić, Tea Martinić Cezar, Béatrice Vallée, Renata Teparić, Igor Stuparević, Bojan Žunar
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Abstract

Yeasts evolved a complex regulatory programme to build and maintain their cell wall, the primary structure through which they interact with their environment. However, how this programme ties to essential cellular processes mostly remains unclear. Here, we focus on Saccharomyces cerevisiae MYND-type zinc finger protein MUB1 (Mub1), an adaptor protein of E3 ubiquitin-protein ligase Ubr2 that was previously associated with regulating proteasome genes through the transcription factor Rpn4. We show that S. cerevisiae cells lacking Mub1 become hyper-tolerant to standard cell wall stressors, outperforming wild-type cells. This protective mub1Δ phenotype stems from the activity of several transcription factors, leading to the inhibition of cell wall remodelling, a typically protective process that becomes maladaptive during chronic cell wall stress in laboratory conditions. Based on these results, we suggest that Mub1 regulates not only Rpn4 but a much broader range of transcription factors, and thus serves as an in-so-far unrecognised regulatory hub directly linking cell wall robustness with the ubiquitin-proteasome system.

Saccharomyces cerevisiae Mub1是E3泛素连接酶Ubr2的底物适配器,通过多种转录因子调节对细胞壁应激源的敏感性。
酵母进化出一个复杂的调节程序来建立和维持它们的细胞壁,细胞壁是它们与环境相互作用的主要结构。然而,这个程序如何与基本的细胞过程联系在一起仍然不清楚。在这里,我们重点研究了酿酒酵母mynd型锌指蛋白MUB1 (MUB1),这是E3泛素蛋白连接酶Ubr2的一种衔接蛋白,以前通过转录因子Rpn4调节蛋白酶体基因。我们发现,缺乏Mub1的酿酒酵母细胞对标准细胞壁应激源具有超耐受性,优于野生型细胞。这种保护性mub1Δ表型源于几种转录因子的活性,导致细胞壁重塑受到抑制,这是一种典型的保护性过程,在实验室条件下,在慢性细胞壁应激过程中变得不适应。基于这些结果,我们认为Mub1不仅调控Rpn4,还调控更广泛的转录因子,因此作为一个迄今未被识别的调控中心,直接将细胞壁稳健性与泛素-蛋白酶体系统联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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