Physical and functional interaction between SET1/COMPASS complex component CFP-1 and a Sin3S HDAC complex in C. elegans

Author:

Beurton Flore1,Stempor Przemyslaw2,Caron Matthieu1,Appert Alex2,Dong Yan2,Chen Ron A-j2,Cluet David1,Couté Yohann3,Herbette Marion1,Huang Ni2,Polveche Hélène4,Spichty Martin1,Bedet Cécile1,Ahringer Julie2,Palladino Francesca1

Affiliation:

1. Laboratory of Biology and Modeling of the Cell, UMR5239 CNRS/Ecole Normale Supérieure de Lyon, INSERM U1210, UMS 3444 Biosciences Lyon Gerland, Université de Lyon, Lyon, France

2. The Gurdon Institute and Department of Genetics, University of Cambridge, Cambridge, UK

3. Grenoble Alpes, CEA, Inserm, BIG-BGE, 38000 Grenoble, France

4. INSERM UMR 861, I-STEM, 28, Rue Henri Desbruères, 91100 Corbeil-Essonnes, France

Abstract

AbstractThe CFP1 CXXC zinc finger protein targets the SET1/COMPASS complex to non-methylated CpG rich promoters to implement tri-methylation of histone H3 Lys4 (H3K4me3). Although H3K4me3 is widely associated with gene expression, the effects of CFP1 loss vary, suggesting additional chromatin factors contribute to context dependent effects. Using a proteomics approach, we identified CFP1 associated proteins and an unexpected direct link between Caenorhabditis elegans CFP-1 and an Rpd3/Sin3 small (SIN3S) histone deacetylase complex. Supporting a functional connection, we find that mutants of COMPASS and SIN3 complex components genetically interact and have similar phenotypic defects including misregulation of common genes. CFP-1 directly binds SIN-3 through a region including the conserved PAH1 domain and recruits SIN-3 and the HDA-1/HDAC subunit to H3K4me3 enriched promoters. Our results reveal a novel role for CFP-1 in mediating interaction between SET1/COMPASS and a Sin3S HDAC complex at promoters.

Funder

Agence Nationale de la Recherche

Fondation ARC

Wellcome Trust Senior Research Fellowship

Wellcome Trust

Cancer Research UK

Proteomics French Infrastructure

Labex GRAL

Publisher

Oxford University Press (OUP)

Subject

Genetics

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