Multistrand Binding of Nuclear Factors to a Repressor of Mouse Mammary Tumor Virus Transcription Can Be Distinguished Kinetically

NRE1 is a DNA sequence element in the long terminal repeat of mouse mammary tumor virus that represses viral transcription in mature T cells. In addition to double-stranded binding activity, factors in Jurkat T cell nuclear extracts bind specifically to each of the two singlestrands of NRE1. Here we...

Full description

Saved in:
Bibliographic Details
Published in:Biochemical and biophysical research communications Vol. 209; no. 1; pp. 379 - 384
Main Authors: Rodda, D.J., Giffin, W., Hache, R.J.G.
Format: Journal Article
Language:English
Published: Elsevier Inc 06-04-1995
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:NRE1 is a DNA sequence element in the long terminal repeat of mouse mammary tumor virus that represses viral transcription in mature T cells. In addition to double-stranded binding activity, factors in Jurkat T cell nuclear extracts bind specifically to each of the two singlestrands of NRE1. Here we show that binding to the three forms of NRE1 can be distinguished kinetically. The on rates for double, upper and lower-strand NRE1 binding were 1.5, 3, and 11 min,respectively. Binding was extremely stable with off-rates varying from 30 and 60 min for double and upper-strand binding to 12 h for lower-strand binding. In addition, a trucated form of NRE1 that is only bound as a double-strand was observed to have an on rate of binding of 4 min and an off rate of 4 h.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.1995.1514