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

Author:

Scully Kathleen M.1,Jacobson Eric M.2,Jepsen Kristen13,Lunyak Victoria1,Viadiu Hector2,Carrière Catherine1,Rose David W.4,Hooshmand Farideh15,Aggarwal Aneel K.2,Rosenfeld Michael G.1

Affiliation:

1. Howard Hughes Medical Institute;

2. Structural Biology Program, Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York, NY 10029, USA.

3. Department of Biology, University of California, San Diego, La Jolla, CA 92093, USA.

4. Department of Endocrinology and Metabolism;

5. Transgenic Research Unit; and Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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