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PMID: 10975253 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of UMP1 is inducible by DNA damage and required for resistance of S. cerevisiae cells to UV light.

Current genetics ·Vol. 38 ·No. 2 ·2000-08-00 ·Pages 53-9

Mieczkowski P, Dajewski W, Podlaska A, Skoneczna A, Ciesla Z, Sledziewska-Gójska E

Abstract

It has recently been shown that the UMP1 gene of Saccharomyces cerevisiae encodes a small. short-lived protein engaged in 20S proteasome formation. The results presented in this paper demonstrate that ULMP1 expression is induced by the DNA damaging agents methyl methanesulfonate (MMS) and UV light as well as by hydroxyurea (HU), an inhibitor of DNA replication. MMS induction of UMP1 expression occurs at the transcriptional level and is independent of the activity of the regulatory checkpoint kinases encoded by MEC1. RAD53 or DUN1. It is also shown that the disruption of UMP1 causes increased sensitivity of yeast cells to killing by UV radiation, but only slight sensitivity to HU treatment, and does not cause any increase in the killing effect of MMS.

MeSH Terms
Cysteine Endopeptidases/metabolism DNA Damage Gene Expression Regulation, Fungal Hydroxyurea/pharmacology Methyl Methanesulfonate/pharmacology Molecular Chaperones/biosynthesis,genetics Multienzyme Complexes/metabolism Mutagens Proteasome Endopeptidase Complex Radiation Tolerance/genetics Saccharomyces cerevisiae/radiation effects Ultraviolet Rays
Chemicals
Molecular Chaperones Multienzyme Complexes Mutagens proteasome maturation protein Methyl Methanesulfonate Cysteine Endopeptidases Proteasome Endopeptidase Complex Hydroxyurea
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mieczkowski P
Institute of Biochemistry and Biophysics, Polish Academy Sceinces, Warsaw.
Dajewski W
Podlaska A
Skoneczna A
Ciesla Z
Sledziewska-Gójska E
Article Info
Journal
Current genetics
Abbr.
Curr Genet
ISSN
0172-8083
Published
2000-08-00
Pages
53-9
Language
English
Region
United States
NLM ID
8004904
Subset
IM
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