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The human nuclear exosome targeting complex is loaded onto newly synthesized RNA to direct early ribonucleolysis

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  • Michal Lubas
  • Peter Refsing Andersen
  • Aleks Schein
  • Andrzej Dziembowski
  • Grzegorz Kudla
  • Torben Heick Jensen

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Original languageEnglish
Pages (from-to)178-92
Number of pages15
JournalCell Reports
Volume10
Issue number2
DOIs
Publication statusPublished - 13 Jan 2015

Abstract

The RNA exosome complex constitutes the major nuclear eukaryotic 3'-5' exonuclease. Outside of nucleoli, the human nucleoplasmic exosome is directed to some of its substrates by the nuclear exosome targeting (NEXT) complex. How NEXT targets RNA has remained elusive. Using an in vivo crosslinking approach, we report global RNA binding sites of RBM7, a key component of NEXT. RBM7 associates broadly with RNA polymerase II-derived RNA, including pre-mRNA and short-lived exosome substrates such as promoter upstream transcripts (PROMPTs), enhancer RNAs (eRNAs), and 3'-extended products from snRNA and replication-dependent histone genes. Within pre-mRNA, RBM7 accumulates at the 3' ends of introns, and pulse-labeling experiments demonstrate that RBM7/NEXT defines an early exosome-targeting pathway for 3'-extended snoRNAs derived from such introns. We propose that RBM7 is generally loaded onto newly synthesized RNA to accommodate exosome action in case of available unprotected RNA 3' ends.

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