Mediator tail subunits can form amyloid-like aggregates in vivo and affect stress response in yeast

被引:20
|
作者
Zhu, Xuefeng [1 ]
Chen, Lihua [2 ]
Carlsten, Jonas O. P. [1 ]
Liu, Qian [2 ]
Yang, Junsheng [2 ]
Liu, Beidong [2 ]
Gustafsson, Claes M. [1 ]
机构
[1] Univ Gothenburg, Inst Biomed, SE-40530 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Chem & Mol Biol, SE-41390 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
ENVIRONMENTAL-STRESS; GENE-EXPRESSION; GLOBAL ANALYSIS; PRION; TRANSCRIPTION; PROTEIN; MODULE; RECRUITMENT; ACTIVATION; MECHANISM;
D O I
10.1093/nar/gkv629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Med2, Med3 and Med15 proteins form a heterotrimeric subdomain in the budding yeast Mediator complex. This Med15 module is an important target for many gene specific transcription activators. A previous proteome wide screen in yeast identified Med3 as a protein with priogenic potential. In the present work, we have extended this observation and demonstrate that both Med3 and Med15 form amyloid-like protein aggregates under H2O2 stress conditions. Amyloid formation can also be stimulated by overexpression of Med3 or of a glutamine-rich domain present in Med15, which in turn leads to loss of the entire Med15 module from Mediator and a change in stress response. In combination with genome wide transcription analysis, our data demonstrate that amyloid formation can change the subunit composition of Mediator and thereby influence transcriptional output in budding yeast.
引用
收藏
页码:7306 / 7314
页数:9
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