Differential Protein Expression in Set5p-Mediated Acetic Acid Stress Response and Novel Targets for Engineering Yeast Stress Tolerance

被引:3
作者
Zhang, Ming-Ming [1 ]
Yuan, Bing [1 ]
Wang, Ya-Ting [1 ]
Zhang, Feng-Li [1 ]
Liu, Chen-Guang [1 ]
Zhao, Xin-Qing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Joint Int Res Lab Metab & Dev Sci, State Key Lab Microbial Metab, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Saccharomyces cerevisiae; histone methyltransferaseSet5p; protein kinase; yeast stress tolerance; chromatin modification; SACCHAROMYCES-CEREVISIAE; PROTEOMIC ANALYSIS; ANALYSIS REVEALS; CELL-WALL; GROWTH; GENE; OVEREXPRESSION; PATHWAYS; COMPLEX; SET5;
D O I
10.1021/acs.jproteome.3c00617
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Acetic acid is a prevalent inhibitor in lignocellulosic hydrolysate, which represses microbial growth and bioproduction. Histone modification and chromatin remodeling have been revealed to be critical for regulating eukaryotic metabolism. However, related studies in chronic acetic acid stress responses remain unclear. Our previous studies revealed that overexpression of the histone H4 methyltransferase Set5p enhanced acetic acid stress tolerance of the budding yeast Saccharomyces cerevisiae. In this study, we examined the role of Set5p in acetic acid stress by analyzing global protein expression. Significant activation of intracellular protein expression under the stress was discovered, and the functions of the differential proteins were mainly involved in chromatin modification, signal transduction, and carbohydrate metabolism. Notably, a substantial increase of Set5p expression was observed in response to acetic acid stress. Functional studies demonstrated that the restriction of the telomere capping protein Rtc3p, as well as Ies3p and Taf14p, which are related to chromatin regulation, was critical for yeast stress response. This study enriches the understanding of the epigenetic regulatory mechanisms underlying yeast stress response mediated by histone-modifying enzymes. The results also benefit the development of robust yeast strains for lignocellulosic bioconversion.
引用
收藏
页码:2986 / 2998
页数:13
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