Mediator tail subunits can form amyloid-like aggregatesin vivoand affect stress response in yeast
Author(s) -
Xuefeng Zhu,
Lihua Chen,
Jonas Carlsten,
Qian Liu,
Junsheng Yang,
Beidong Liu,
Claes M. Gustafsson
Publication year - 2015
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkv629
Subject(s) - mediator , biology , heterotrimeric g protein , microbiology and biotechnology , protein subunit , yeast , transcription (linguistics) , proteome , saccharomyces cerevisiae , gene , genetics , signal transduction , g protein , linguistics , philosophy
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.
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