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PMID: 2302185 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Characterization of the human immunodeficiency virus type 1 enhancer-binding proteins from the human T-cell line Jurkat.

The Biochemical journal ·Vol. 265 ·No. 2 ·1990-01-15 ·Pages 547-54

Korner M, Bellan AH, Brini AT, Farrar WL

Abstract

The transcription of the human immunodeficiency virus type 1 (HIV-1) is under the control of cellular proteins that bind to the viral long terminal repeat (LTR). Among the protein-binding regions of the HIV-1 LTR is the transcription-enhancer region. We show that at least one inducible, C1, and one constitutive, C2, protein can bind to the HIV enhancer in Jurkat cells. The two proteins differ in their surface charge, since they are separable by anion-exchange chromatography. Bivalent cations such as Mg2+ and Zn2+ differentially affect their binding to oligonucleotides which contain the HIV-enhancer domain. Both C1 and C2 proteins also bind to a similar sequence found in the interleukin-2-receptor alpha-subunit enhancer. The inducible C1 protein was partially purified by three chromatographic steps and characterized by u.v. cross-linking as a 47 kDa protein.

MeSH Terms
Base Sequence Cell Line Chromatography, Affinity Chromatography, DEAE-Cellulose Chromatography, High Pressure Liquid DNA-Binding Proteins/biosynthesis,isolation & purification,metabolism Enhancer Elements, Genetic HIV-1/genetics,metabolism Humans Molecular Sequence Data Molecular Weight Oligonucleotide Probes T-Lymphocytes Transcription Factors/biosynthesis,isolation & purification,metabolism Transcription, Genetic
Chemicals
DNA-Binding Proteins Oligonucleotide Probes Transcription Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Korner M
BCDP, Program Resources, Inc., NCI--Frederick Cancer Research Facility, MD.
Bellan A H
Brini A T
Farrar W L
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1990-01-15
Pages
547-54
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1136918
Subset
IM
Grants
NCI NIH HHS · N01-CO-74102 · United States
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