RNA Targets Ribogenesis Factor WDR43 to Chromatin for Transcription and Pluripotency Control

Mol Cell. 2019 Jul 11;75(1):102-116.e9. doi: 10.1016/j.molcel.2019.05.007. Epub 2019 May 22.

Abstract

Transcription regulation underlies stem cell function and development. Here, we elucidate an unexpected role of an essential ribogenesis factor, WDR43, as a chromatin-associated RNA-binding protein (RBP) and release factor in modulating the polymerase (Pol) II activity for pluripotency regulation. WDR43 binds prominently to promoter-associated noncoding/nascent RNAs, occupies thousands of gene promoters and enhancers, and interacts with the Pol II machinery in embryonic stem cells (ESCs). Nascent transcripts and transcription recruit WDR43 to active promoters, where WDR43 facilitates releases of the elongation factor P-TEFb and paused Pol II. Knockdown of WDR43 causes genome-wide defects in Pol II release and pluripotency-associated gene expression. Importantly, auxin-mediated rapid degradation of WDR43 drastically reduces Pol II activity, precluding indirect consequences. These results reveal an RNA-mediated recruitment and feedforward regulation on transcription and demonstrate an unforeseen role of an RBP in promoting Pol II elongation and coordinating high-level transcription and translation in ESC pluripotency.

Keywords: Pol II; RBP; RNA; WDR43; chromatin; promoter; transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Cation Transport Proteins / genetics*
  • Cation Transport Proteins / metabolism
  • Cell Differentiation
  • Cell Line
  • Chromatin / chemistry*
  • Chromatin / metabolism
  • Embryo, Mammalian
  • Enhancer Elements, Genetic
  • Gene Deletion
  • Gene Expression Regulation, Developmental*
  • Human Embryonic Stem Cells / cytology
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mouse Embryonic Stem Cells / cytology
  • Mouse Embryonic Stem Cells / metabolism*
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / metabolism
  • Positive Transcriptional Elongation Factor B / genetics
  • Positive Transcriptional Elongation Factor B / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Biosynthesis
  • Proteolysis
  • RNA Polymerase II / genetics*
  • RNA Polymerase II / metabolism
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / genetics*
  • RNA-Binding Proteins / metabolism
  • Signal Transduction
  • Transcription, Genetic*
  • Zebrafish Proteins / genetics*
  • Zebrafish Proteins / metabolism

Substances

  • Cation Transport Proteins
  • Chromatin
  • RNA, Messenger
  • RNA-Binding Proteins
  • WDR43 protein, human
  • Zebrafish Proteins
  • slc39a6 protein, zebrafish
  • Positive Transcriptional Elongation Factor B
  • RNA Polymerase II