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PMID: 9724713 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Overexpression of the large subunit of the protein Ku suppresses metallothionein-I induction by heavy metals.

Ghoshal K, Li Z, Jacob ST

Abstract

Metallothioneins (MT) are involved in the scavenging of the toxic heavy metals and protection of cells from reactive oxygen intermediates. To investigate the potential role of the protein Ku in the expression of MT, we measured the level of MT-I mRNA in the parental rat fibroblast cell line (Rat 1) and the cell lines that stably and constitutively overexpress the small subunit, the large subunit, and the heterodimer of Ku. Treatment with CdS04 or ZnS04 elevated the MT-I mRNA level 20- to 30-fold in the parental cells and the cells (Ku-70) that overproduce the small subunit or those (Ku-7080) overexpressing the heterodimer. By contrast, the cells (Ku-80) overexpressing the large subunit of Ku failed to induce MT-I. In vitro transcription assay showed that the MT-I promoter activity was suppressed selectively in the nuclear extracts from Ku-80 cells. The specificity of the repressor function was shown by the induction of hsp 70, another Cd-inducible gene, in Ku-80 cells. Addition of the nuclear extract from Ku-80 cells at the start of the transcription reaction abolished the MT-l promoter activity in the Rat 1 cell extract. The transcript once formed in Rat 1 nuclear extract was not degraded by further incubation with the extract from Ku-80 cells. The repressor was sensitive to heat. The DNA-binding activities of at least four transcription factors that control the MT-I promoter activity were not affected in Ku-80 cells. These observations have set the stage for further exploration of the mechanisms by which the Ku subunit mediates suppression of MT induction.

MeSH Terms
Animals Antigens, Nuclear Cell Line Cell Nucleus/metabolism DNA Helicases DNA-Binding Proteins/chemistry,genetics Dimerization Gene Expression Regulation/drug effects Ku Autoantigen Metallothionein/biosynthesis,genetics Metals/pharmacology Mice Nuclear Proteins/chemistry,genetics Promoter Regions, Genetic RNA, Messenger/genetics Rats Saccharomyces cerevisiae Proteins Transcription Factors/chemistry,genetics Transcription, Genetic
Chemicals
Antigens, Nuclear DNA-Binding Proteins Metals Nuclear Proteins RNA, Messenger Saccharomyces cerevisiae Proteins Transcription Factors high affinity DNA-binding factor, S cerevisiae Metallothionein DNA Helicases XRCC5 protein, human Xrcc6 protein, human Xrcc6 protein, mouse Xrcc6 protein, rat Ku Autoantigen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ghoshal K
Department of Medical Biochemistry, The Ohio State University, College of Medicine, 333 Hamilton Hall, 1645 Neil Avenue, Columbus, OH 43210, USA.
Li Z
Jacob S T
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1998-09-01
Pages
10390-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC27904
Subset
IM
Grants
NCI NIH HHS · CA 61321 · United States
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