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PMID: 2581314 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification of human glucocorticoid receptor complementary DNA clones by epitope selection.

Science (New York, N.Y.) ·Vol. 228 ·No. 4700 ·1985-05-10 ·Pages 740-2

Weinberger C, Hollenberg SM, Ong ES, Harmon JM, Brower ST, Cidlowski J, Thompson EB, Rosenfeld MG, Evans RM

Abstract

Steroid hormones regulate cellular differentiation and physiologic functions predominantly through gene transcription. Regulation is achieved by the interaction of specific steroid receptor proteins and target genes. Expression cloning techniques were used to select human glucocorticoid receptor complementary DNA clones in order to define the mechanism by which the receptor exerts its transcriptional control. Immobilized fusion proteins from individual clones were used to select epitope-specific antibody which was subsequently eluted and identified by binding to protein blots of cellular extracts. Three cross-hybridizing clones containing inserts expressing antigenic determinants of the human glucocorticoid receptor were isolated.

MeSH Terms
Cloning, Molecular DNA/genetics DNA, Recombinant/metabolism Epitopes/genetics,immunology Humans Receptors, Glucocorticoid/genetics,immunology Receptors, Steroid/genetics Transcription, Genetic
Chemicals
DNA, Recombinant Epitopes Receptors, Glucocorticoid Receptors, Steroid DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Weinberger C
Hollenberg S M
Ong E S
Harmon J M
Brower S T
Cidlowski J
Thompson E B
Rosenfeld M G
Evans R M
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1985-05-10
Pages
740-2
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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