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PMID: 2996140 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Functional relation between HTLV-II x and adenovirus E1A proteins in transcriptional activation.

Science (New York, N.Y.) ·Vol. 230 ·No. 4725 ·1985-11-01 ·Pages 570-3

Chen IS, Cann AJ, Shah NP, Gaynor RB

Abstract

The mechanism of cellular transformation by the human T-cell leukemia viruses (HTLV) is thought to involve a novel gene known as the x gene. This gene is essential for HTLV replication and acts by enhancing transcription from the HTLV long terminal repeat. The HTLV x gene product may also cause aberrant transcription of normal cellular genes, resulting in transformation of the infected cells. Although there is no evidence as yet for such a mechanism, it was shown that the HTLV-II x gene product can activate transcription from adenovirus E1A-dependent early promoters and therefore has the potential to activate cellular genes. It was also shown that the adenovirus and herpes pseudorabies immediate early proteins activate expression from the HTLV-I and HTLV-II long terminal repeats, though at lower levels than with the x gene product. These findings indicate possible common mechanisms of action for transcription-regulatory genes of distinct viruses.

MeSH Terms
Adenoviridae/genetics Cell Transformation, Viral Deltaretrovirus/genetics Endonucleases/metabolism HeLa Cells Herpesvirus 4, Human Humans Operon Repetitive Sequences, Nucleic Acid Single-Strand Specific DNA and RNA Endonucleases Transcription, Genetic/drug effects Transfection Viral Proteins/pharmacology
Chemicals
Viral Proteins Endonucleases Single-Strand Specific DNA and RNA Endonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chen I S
Cann A J
Shah N P
Gaynor R B
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1985-11-01
Pages
570-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · CA 16042 · United States
NCI NIH HHS · CA 32737 · United States
NCI NIH HHS · CA 38597 · United States
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