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PMID: 3428603 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The major late transcription factor binds to and activates the mouse metallothionein I promoter.

Genes & development ·Vol. 1 ·No. 9 ·1987-11-00 ·Pages 973-80

Carthew RW, Chodosh LA, Sharp PA

Abstract

Human (HeLa) cells contain a protein, MLTF, which specifically binds to a DNA sequence in the adenovirus 2 major late promoter and activates transcription of that promoter. The presence of MLTF in uninfected cells suggests that this factor contributes to the transcription of some cellular genes. We find that MLTF binds in a sequence-specific manner to the 5'-flanking region of the mouse metallothionein I (mMTI) gene. Binding was localized between -101 and -94 (relative to the initiation site at +1) by DNA-binding gel electrophoresis assay and DNA methylation interference analysis. As in adenovirus, binding occurred in a region containing the sequence CPuCGTGAC. Deletion of this sequence both eliminated the binding of MLTF and produced a fourfold reduction in transcriptional efficiency in vitro. In contrast to the intact promoter, transcription from the deletion mutant promoter was not stimulated by addition of purified MLTF to an in vitro reconstituted reaction. These results suggest that MLTF contributes to the transcription of cellular genes.

MeSH Terms
Adenoviruses, Human/genetics Base Sequence Genes HeLa Cells/metabolism Humans Metallothionein/genetics Methylation Plasmids Promoter Regions, Genetic Transcription Factors/metabolism Transcription, Genetic
Chemicals
Transcription Factors Metallothionein
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Carthew R W
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Chodosh L A
Sharp P A
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
1987-11-00
Pages
973-80
Language
English
Region
United States
NLM ID
8711660
Subset
IM
Grants
NCI NIH HHS · P01-CA42063 · United States
NCI NIH HHS · P30-CA14051 · United States
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