Home LiteratureArticle Details
PMID: 11073444 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Allosteric effects of Pit-1 DNA sites on long-term repression in cell type specification.

Science (New York, N.Y.) ·Vol. 290 ·No. 5494 ·2000-11-10 ·Pages 1127-31

Scully KM, Jacobson EM, Jepsen K, Lunyak V, Viadiu H, Carrière C, Rose DW, Hooshmand F, Aggarwal AK, Rosenfeld MG

Abstract

Reciprocal gene activation and restriction during cell type differentiation from a common lineage is a hallmark of mammalian organogenesis. A key question, then, is whether a critical transcriptional activator of cell type-specific gene targets can also restrict expression of the same genes in other cell types. Here, we show that whereas the pituitary-specific POU domain factor Pit-1 activates growth hormone gene expression in one cell type, the somatotrope, it restricts its expression from a second cell type, the lactotrope. This distinction depends on a two-base pair spacing in accommodation of the bipartite POU domains on a conserved growth hormone promoter site. The allosteric effect on Pit-1, in combination with other DNA binding factors, results in the recruitment of a corepressor complex, including nuclear receptor corepressor N-CoR, which, unexpectedly, is required for active long-term repression of the growth hormone gene in lactotropes.

MeSH Terms
Allosteric Regulation Animals Base Sequence Binding Sites Cell Line Conserved Sequence Crystallization DNA/metabolism DNA-Binding Proteins/chemistry,genetics,metabolism Female Gene Expression Regulation Genes, Reporter Growth Hormone/genetics Male Mice Mice, Transgenic Models, Molecular Molecular Sequence Data Nuclear Proteins/genetics,metabolism Nuclear Receptor Co-Repressor 1 Pituitary Gland/cytology,metabolism Prolactin/genetics Promoter Regions, Genetic Protein Conformation Protein Structure, Tertiary Rats Repressor Proteins/chemistry,genetics,metabolism Transcription Factor Pit-1 Transcription Factors/chemistry,genetics,metabolism Transcriptional Activation
Chemicals
DNA-Binding Proteins Ncor1 protein, mouse Ncor1 protein, rat Nuclear Proteins Nuclear Receptor Co-Repressor 1 Pit1 protein, mouse Pou1f1 protein, rat Repressor Proteins Transcription Factor Pit-1 Transcription Factors Prolactin Growth Hormone DNA
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Scully K M
Howard Hughes Medical Institute, Department of Endocrinology and Metabolism, School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Jacobson E M
Jepsen K
Lunyak V
Viadiu H
Carrière C
Rose D W
Hooshmand F
Aggarwal A K
Rosenfeld M G
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
2000-11-10
Pages
1127-31
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDDK NIH HHS · R01 DK18477 · United States
NIDDK NIH HHS · R01 DK54802 · United States
NIGMS NIH HHS · R01 GM49327 · United States
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