eLife (Dec 2017)

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

  • Xinan H Yang,
  • Rangarajan D Nadadur,
  • Catharina RE Hilvering,
  • Valerio Bianchi,
  • Michael Werner,
  • Stefan R Mazurek,
  • Margaret Gadek,
  • Kaitlyn M Shen,
  • Joseph Aaron Goldman,
  • Leonid Tyan,
  • Jenna Bekeny,
  • Johnathon M Hall,
  • Nutishia Lee,
  • Carlos Perez-Cervantes,
  • Ozanna Burnicka-Turek,
  • Kenneth D Poss,
  • Christopher R Weber,
  • Wouter de Laat,
  • Alexander J Ruthenburg,
  • Ivan P Moskowitz

DOI
https://doi.org/10.7554/eLife.31683
Journal volume & issue
Vol. 6

Abstract

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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.

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