Transcription-factor-dependent enhancer transcription defines a gene regulatory network for cardiac rhythm

Author:

Yang Xinan H123,Nadadur Rangarajan D123,Hilvering Catharina RE4,Bianchi Valerio4ORCID,Werner Michael56,Mazurek Stefan R123,Gadek Margaret123,Shen Kaitlyn M123,Goldman Joseph Aaron78,Tyan Leonid123,Bekeny Jenna123,Hall Johnathon M56,Lee Nutishia7,Perez-Cervantes Carlos123,Burnicka-Turek Ozanna123,Poss Kenneth D78,Weber Christopher R123,de Laat Wouter4,Ruthenburg Alexander J56ORCID,Moskowitz Ivan P123ORCID

Affiliation:

1. Department of Pediatrics, The University of Chicago, Chicago, United States

2. Department of Pathology, The University of Chicago, Chicago, United States

3. Department of Human Genetics, The University of Chicago, Chicago, United States

4. Hubrecht Institute-Koninklijke Nederlandse Akademie van Wetenschappen, University Medical Center Utrecht, Uppsalalaan, Netherlands

5. Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States

6. Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, United States

7. Department of Cell Biology, Duke University School of Medicine, Durham, United States

8. Regeneration Next, Duke University, Durham, United States

Abstract

The noncoding genome is pervasively transcribed. Noncoding RNAs (ncRNAs) generated from enhancers have been proposed as a general facet of enhancer function and some have been shown to be required for enhancer activity. Here we examine the transcription-factor-(TF)-dependence of ncRNA expression to define enhancers and enhancer-associated ncRNAs that are involved in a TF-dependent regulatory network. TBX5, a cardiac TF, regulates a network of cardiac channel genes to maintain cardiac rhythm. We deep sequenced wildtype and Tbx5-mutant mouse atria, identifying ~2600 novel Tbx5-dependent ncRNAs. Tbx5-dependent ncRNAs were enriched for tissue-specific marks of active enhancers genome-wide. Tbx5-dependent ncRNAs emanated from regions that are enriched for TBX5-binding and that demonstrated Tbx5-dependent enhancer activity. Tbx5-dependent ncRNA transcription provided a quantitative metric of Tbx5-dependent enhancer activity, correlating with target gene expression. We identified RACER, a novel Tbx5-dependent long noncoding RNA (lncRNA) required for the expression of the calcium-handling gene Ryr2. We illustrate that TF-dependent enhancer transcription can illuminate components of TF-dependent gene regulatory networks.

Funder

National Institutes of Health

Fondation Leducq

American Heart Association

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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