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PMID: 2575384 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

A protein target site in an early replicated human DNA sequence: a highly conserved binding motif.

Biochemical and biophysical research communications ·Vol. 165 ·No. 3 ·1989-12-29 ·Pages 956-65

Giacca M, Gutierrez MI, Demarchi F, Diviacco S, Biamonti G, Riva S, Falaschi A

Abstract

We have previously reported that a human nuclear factor, probably corresponding to the USF/MLTF protein [1,2], is able to bind specifically to a DNA sequence present in DNA replicated at the onset of S-phase [3]. Here we demonstrate that the same factor binds also to several other similar sequences, present in eukaryotic and viral genomes. Mutations or methylation in a CpG dinucleotide, central in the palindromic binding site, completely abolish binding. Furthermore, we present evidence for the existence of at least two other nuclear proteins in human cells with the same DNA binding specificity. The data presented suggest a strong evolutionary conservation, among distantly related organisms, of the binding motif, which is probably the target of a number of nuclear factors that share the same DNA binding specificity albeit in the context of different functions.

MeSH Terms
Base Composition Base Sequence Binding Sites Binding, Competitive DNA/metabolism DNA Replication Drug Stability Genes, Homeobox HeLa Cells Hot Temperature Humans Methylation Molecular Sequence Data Mutation Nuclear Proteins/metabolism Oligonucleotides/metabolism Tumor Cells, Cultured
Chemicals
Nuclear Proteins Oligonucleotides DNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Giacca M
International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Gutierrez M I
Demarchi F
Diviacco S
Biamonti G
Riva S
Falaschi A
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1989-12-29
Pages
956-65
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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