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Polymerase eta is a short-lived, proteasomally degraded protein that is temporarily stabilized following UV irradiation in Saccharomyces cerevisiae.

Abstract
Saccharomyces cerevisiae Rad30 is the homolog of human DNA polymerase eta whose inactivation leads to the cancer-prone syndrome xeroderma pigmentosum variant. Both human and yeast polymerase eta are responsible for error-free bypass of UV-induced cis-syn pyrimidine dimers and several other DNA lesions. Here we show, using yeast strains expressing TAP-tagged Rad30, that the level of this protein is post-translationally regulated via ubiquitination and proteasome-mediated degradation. The half-life of Rad30 is 20 min and it increases due to proteasomal defects. Mutations inactivating components of the Skp1/cullin/ F-box (SCF) ubiquitin ligase complex: Skp1 and the F-box protein Ufo1 stabilize Rad30. Our results indicate also that ultraviolet irradiation causes transient stabilization of Rad30, which leads, in turn, to temporary accumulation of this polymerase in the cell. We conclude that proteolysis plays an important role in regulating the cellular abundance of Rad30. These results are the first indication of a role for controlled proteasomal degradation in modulating cellular level of translesion DNA polymerase in eukaryotes.
AuthorsAdrianna Skoneczna, Justyna McIntyre, Marek Skoneczny, Zofia Policinska, Ewa Sledziewska-Gojska
JournalJournal of molecular biology (J Mol Biol) Vol. 366 Issue 4 Pg. 1074-86 (Mar 02 2007) ISSN: 0022-2836 [Print] Netherlands
PMID17198712 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Saccharomyces cerevisiae Proteins
  • DNA-Directed DNA Polymerase
  • Rad30 protein
  • Proteasome Endopeptidase Complex
Topics
  • DNA-Directed DNA Polymerase (metabolism)
  • Enzyme Stability
  • Gene Expression Regulation, Enzymologic
  • Proteasome Endopeptidase Complex (metabolism, physiology, radiation effects)
  • Saccharomyces cerevisiae (enzymology, radiation effects)
  • Saccharomyces cerevisiae Proteins (metabolism)
  • Ultraviolet Rays

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