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PMID: 2826819 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

A DNA element responsible for the different tissue specificities of Friend and Moloney retroviral enhancers.

Journal of virology ·Vol. 62 ·No. 2 ·1988-02-00 ·Pages 614-8

Thiesen HJ, Bösze Z, Henry L, Charnay P

Abstract

The transcriptional enhancers of the Moloney murine sarcoma virus (MuSV) and Moloney murine leukemia virus (MuLV) have different cell type specificities from that of the Friend MuLV. While the three enhancers are approximately equally active in erythroid cells, the Moloney MuSV and Moloney MuLV enhancers are 20- to 40-fold more active than the Friend MuLV enhancer in T-lymphoid cells. Using mutant enhancers, we have shown that specific differences between the nucleotide sequences of the Moloney MuSV and Friend MuLV enhancers are responsible for their different activities in T cells. Our data allow the localization of a DNA element, repeated several times within the enhancer, which modulates the activity of the enhancer in T cells without affecting it in erythroid cells. This element therefore appears to be one of the determinants of the tissue specificity of the enhancer.

MeSH Terms
Base Sequence Cell Line DNA, Viral/genetics Enhancer Elements, Genetic Erythrocytes/microbiology Friend murine leukemia virus/genetics Humans Molecular Sequence Data Moloney murine leukemia virus/genetics Moloney murine sarcoma virus/genetics Mutation Sarcoma Viruses, Murine/genetics T-Lymphocytes/microbiology Transfection
Chemicals
DNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Thiesen H J
Differentiation Programme, European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Bösze Z
Henry L
Charnay P
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19 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1988-02-00
Pages
614-8
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC250577
Subset
IM
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