RNA turnover in human mitochondria: more questions than answers?

Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):1066-70. doi: 10.1016/j.bbabio.2010.01.028. Epub 2010 Feb 2.

Abstract

Protein complexes responsible for RNA degradation play important role in three key aspects of RNA metabolism: they control stability of physiologically functional transcripts, remove the unnecessary RNA processing intermediates and destroy aberrantly formed RNAs. In mitochondria the post-transcriptional events seem to play a major role in regulation of gene expression, therefore RNA turnover is of particular importance. Despite many years of research, the details of this process are still a challenge. This review summarizes emerging landscape of interplay between the Suv3p helicase (SUPV3L1, Suv3), poly(A) polymerase and polynucleotide phosphorylase in controlling RNA degradation in human mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • DEAD-box RNA Helicases / metabolism
  • Humans
  • In Vitro Techniques
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Models, Biological
  • Poly U / metabolism
  • Polyadenylation
  • Polynucleotide Adenylyltransferase / metabolism
  • Polyribonucleotide Nucleotidyltransferase / metabolism
  • RNA / genetics
  • RNA / metabolism*
  • RNA Processing, Post-Transcriptional
  • RNA Stability
  • RNA, Fungal / genetics
  • RNA, Fungal / metabolism
  • RNA, Mitochondrial
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism

Substances

  • RNA, Fungal
  • RNA, Mitochondrial
  • Poly U
  • RNA
  • Polynucleotide Adenylyltransferase
  • Polyribonucleotide Nucleotidyltransferase
  • SUPV3L1 protein, human
  • DEAD-box RNA Helicases