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The role of deadenylation in the degradation of unstable mRNAs in trypanosomes

  • Angela Schwede
  • , Theresa Manful
  • , Bhaskar Anand Jha
  • , Claudia Helbig
  • , Natalia Bercovich
  • , Mhairi Stewart
  • , Christine Clayton
  • Heidelberg University 
  • Universidad de Buenos Aires
  • University of Glasgow

Research output: Contribution to journalArticlepeer-review

59 Citations (Scopus)

Abstract

Removal of the poly(A) tail is the first step in the degradation of many eukaryotic mRNAs. In metazoans and yeast, the Ccr4/Caf1/Not complex has the predominant deadenylase activity, while the Pan2/Pan3 complex may trim poly(A) tails to the correct size, or initiate deadenylation. In trypanosomes, turnover of several constitutively-expressed or long-lived mRNAs is not affected by depletion of the 5'-3' exoribonuclease XRNA, but is almost completely inhibited by depletion of the deadenylase CAF1. In contrast, two highly unstable mRNAs, encoding EP procyclin and a phosphoglycerate kinase, PGKB, accumulate when XRNA levels are reduced. We here show that degradation of EP mRNA was partially inhibited after CAF1 depletion. RNAi-targeting trypanosome PAN2 had a mild effect on global deadenylation, and on degradation of a few mRNAs including EP. By amplifying and sequencing degradation intermediates, we demonstrated that a reduction in XRNA had no effect on degradation of a stable mRNA encoding a ribosomal protein, but caused accumulation of EP mRNA fragments that had lost substantial portions of the 5' and 3' ends. The results support a model in which trypanosome mRNAs can be degraded by at least two different, partially independent, cytoplasmic degradation pathways attacking both ends of the mRNA.

Original languageEnglish
Article numbergkp571
Pages (from-to)5511-5528
Number of pages18
JournalNucleic Acids Research
Volume37
Issue number16
DOIs
Publication statusPublished - 13 Jul 2009
Externally publishedYes

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