Important note: Information in this article was accurate in 1996. The state of the art may have changed since the publication date.
Sequence requirements of ATF2 and CREB binding to the human T-cell leukemia virus type 1 LTR R region.
Virology. 1996 Apr 15;218(2):362-71. Unique Identifier : AIDSLINE MED/96193748 Xu X; Kang SH; Heidenreich O; Brown DA; Nerenberg MI; Department of Molecular and Experimental Medicine, Scripps; Research Institute, La Jolla, California 92037, USA.
Abstract:
We have identified crucial transcription factor contact sites within the distal portion of the HTLV-1 LTR R region. Single base substitutions within this region greatly reduce formation of a complex which we previously described as a 70-kDa nuclear protein interacting with a CREB-like protein. Comparison of published sequences of HTLV-1 isolates obtained from scattered geographic locations revealed that clustered mutations in an 8-base segment near the U5 junction do, in fact, occur naturally. A single base substitution corresponding to a common naturally occurring mutation was introduced into the R region of an HTLV-1-LTR Cat construct. This resulted in derepression of the promoter in a cell line expressing high levels of the R region binding complex when compared to the wild-type LTR promoter. Affinity purification and electrophoretic mobility super-shift analysis identified a dominant 70-kDa DNA binding protein as ATF-2. Phosphorylated ATF-2 apparently interacts with CREB to form this downstream complex.
Keywords: Base Sequence DNA Mutational Analysis DNA-Binding Protein, Cyclic AMP-Responsive/CHEMISTRY/*METABOLISM DNA, Viral/*GENETICS/METABOLISM Human HTLV-I/*GENETICS HTLV-I Infections/VIROLOGY Methylation Molecular Sequence Data Molecular Weight Phosphorylation Point Mutation/GENETICS Promoter Regions (Genetics)/GENETICS Protein Binding Repetitive Sequences, Nucleic Acid/*GENETICS Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. Transcription Factors/CHEMISTRY/*METABOLISM JOURNAL ARTICLE 960830
M9681131
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