Tissue-Specific Regulation of Retinal and Pituitary Precursor Cell Proliferation

Author:

Li Xue1,Perissi Valentina1,Liu Forrest1,Rose David W.2,Rosenfeld Michael G.1

Affiliation:

1. Howard Hughes Medical Institute, Department of Molecular Medicine, University of California, San Diego, School of Medicine, 9500 Gilman Drive, Room 345, La Jolla, CA 92093–0648, USA.

2. Department of Endocrinology and Metabolism, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093–0673, USA.

Abstract

Mammalian organogenesis requires the expansion of pluripotent precursor cells before the subsequent determination of specific cell types, but the tissue-specific molecular mechanisms that regulate the initial expansion of primordial cells remain poorly defined. We have genetically established that Six6 homeodomain factor, acting as a strong tissue-specific repressor, regulates early progenitor cell proliferation during mammalian retinogenesis and pituitary development. Six6, in association with Dach corepressors, regulates proliferation by directly repressing cyclin-dependent kinase inhibitors, including the p27Kip1 promoter. These data reveal a molecular mechanism by which a tissue-specific transcriptional repressor-corepressor complex can provide an organ-specific strategy for physiological expansion of precursor populations.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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