Chromatin targeting of the RNF12/RLIM E3 ubiquitin ligase controls transcriptional responses

Author:

Espejo-Serrano Carmen1ORCID,Aitken Catriona1,Tan Beatrice F2ORCID,May Danielle G3ORCID,Chrisopulos Rachel J3,Roux Kyle J34ORCID,Demmers Jeroen AA5,Mackintosh Samuel G6,Gribnau Joost2,Bustos Francisco47ORCID,Gontan Cristina2ORCID,Findlay Greg M1ORCID

Affiliation:

1. MRC Protein Phosphorylation and Ubiquitylation Unit

2. Department of Developmental Biology, Erasmus University Medical Center

3. Enabling Technologies Group, Sanford Research

4. Department of Pediatrics, Sanford School of Medicine, University of South Dakota, Sioux Falls, SD, USA

5. Proteomics Center and Department of Biochemistry, Erasmus University Medical Center

6. Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA

7. Pediatrics and Rare Diseases Group, Sanford Research

Abstract

Protein ubiquitylation regulates key biological processes including transcription. This is exemplified by the E3 ubiquitin ligase RNF12/RLIM, which controls developmental gene expression by ubiquitylating the REX1 transcription factor and is mutated in an X-linked intellectual disability disorder. However, the precise mechanisms by which ubiquitylation drives specific transcriptional responses are not known. Here, we show that RNF12 is recruited to specific genomic locations via a consensus sequence motif, which enables co-localisation with REX1 substrate at gene promoters. Surprisingly, RNF12 chromatin recruitment is achieved via a non-catalytic basic region and comprises a previously unappreciated N-terminal autoinhibitory mechanism. Furthermore, RNF12 chromatin targeting is critical for REX1 ubiquitylation and downstream RNF12-dependent gene regulation. Our results demonstrate a key role for chromatin in regulation of the RNF12-REX1 axis and provide insight into mechanisms by which protein ubiquitylation enables programming of gene expression.

Funder

Wellcome Trust

Wellcome Trust/Royal Society Sir Henry Dale Fellowship

Dutch Research Council

National Institutes of Health

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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