An HSF1–JMJD6–HSP feedback circuit promotes cell adaptation to proteotoxic stress

Author:

Alasady Milad J.123ORCID,Koeva Martina456,Takagishi Seesha R.123,Segal Dmitri7,Amici David R.123ORCID,Smith Roger S.123ORCID,Ansel Daniel J.123,Lindquist Susan456,Whitesell Luke45,Bartom Elizabeth T.123,Taipale Mikko7ORCID,Mendillo Marc L.123

Affiliation:

1. Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611

2. Simpson Querrey Center for Epigenetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611

3. Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611

4. Whitehead Institute for Biomedical Research, Cambridge, MA 02142

5. Massachusetts Institute of Technology, Cambridge, MA 02142

6. HHMI, Cambridge, MA 02139

7. Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada

Abstract

Heat Shock Factor 1 (HSF1) is best known as the master transcriptional regulator of the heat-shock response (HSR), a conserved adaptive mechanism critical for protein homeostasis (proteostasis). Combining a genome-wide RNAi library with an HSR reporter, we identified Jumonji domain-containing protein 6 (JMJD6) as an essential mediator of HSF1 activity. In follow-up studies, we found that JMJD6 is itself a noncanonical transcriptional target of HSF1 which acts as a critical regulator of proteostasis. In a positive feedback circuit, HSF1 binds and promotes JMJD6 expression, which in turn reduces heat shock protein 70 (HSP70) R469 monomethylation to disrupt HSP70–HSF1 repressive complexes resulting in enhanced HSF1 activation. Thus, JMJD6 is intricately wired into the proteostasis network where it plays a critical role in cellular adaptation to proteotoxic stress.

Funder

Foundation for the National Institutes of Health

HHS | NIH | National Cancer Institute

Publisher

Proceedings of the National Academy of Sciences

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