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PMID: 1530615 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Sequence-specific binding of HMG-I(Y) to the proximal promoter of the gp91-phox gene.

Biochemical and biophysical research communications ·Vol. 187 ·No. 2 ·1992-09-16 ·Pages 563-9

Skalnik DG, Neufeld EJ

Abstract

Screening of a cDNA expression library with a CCAAT-box element derived from the myelomonocyte-specific gp91-phox promoter resulted in the isolation of three independent HMG-I(Y) cDNA clones. Filter binding competition studies reveal that HMG-Y binds to this promoter element in a sequence-specific manner and exhibits a gradient of binding affinities for various A/T-rich sequences. Two adjacent A/T-rich regions within the gp91-phox promoter CCAAT-box element are required for maximal binding. In addition, competition experiments demonstrate that the binding affinity of HMG-Y is influenced by sequences that flank A/T-rich core binding sites.

MeSH Terms
Base Sequence Binding Sites Binding, Competitive Cloning, Molecular DNA/chemistry,isolation & purification,metabolism High Mobility Group Proteins/metabolism Molecular Sequence Data NADH, NADPH Oxidoreductases/genetics NADPH Oxidases Promoter Regions, Genetic
Chemicals
High Mobility Group Proteins DNA NADH, NADPH Oxidoreductases NADPH Oxidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Skalnik D G
Division of Hematology/Oncology, Children's Hospital, Dana-Farber Cancer Institute, Boston, MA.
Neufeld E J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1992-09-16
Pages
563-9
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Corrections
ErratumIn
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