Allosteric Effects of Pit-1 DNA Sites on Long-Term Repression in Cell Type Specification

Kathleen M. Scully(Howard Hughes Medical Institute), Eric M. Jacobson(Icahn School of Medicine at Mount Sinai), Kristen Jepsen(Howard Hughes Medical Institute), Victoria V. Lunyak(Howard Hughes Medical Institute), Héctor Viadiu(Icahn School of Medicine at Mount Sinai), Catherine Carrière(Howard Hughes Medical Institute), David W. Rose, Farideh Hooshmand(Howard Hughes Medical Institute), Aneel K. Aggarwal(Icahn School of Medicine at Mount Sinai), Michael G. Rosenfeld(Howard Hughes Medical Institute)
Science
November 10, 2000
Cited by 246

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.


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