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Molecular and Cellular Biology, October 2007, p. 6770-6781, Vol. 27, No. 19
0270-7306/07/$08.00+0 doi:10.1128/MCB.00479-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Dipartimento di Sanità Pubblica e Biologia Cellulare, Università di Roma Tor Vergata, Rome, Italy,1 Cancer Biology and Genetics Program, Department of Pathology, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021,2 Dipartimento di Biotecnologie e Bioscienze, Universit à Milano-Bicocca, Milan, Italy,3 Dipartimento di Medicina Sperimentale, Università dell'Aquila, L'Aquila, Italy4
Received 20 March 2007/ Returned for modification 30 April 2007/ Accepted 19 July 2007
Male mice lacking expression of Plzf, a DNA sequence-specific transcriptional repressor, show progressive germ cell depletion due to exhaustion of the spermatogonial stem cell population. This is likely due to the deregulated expression of genes controlling the switch between spermatogonial self-renewal and differentiation. Here we show that Plzf directly represses the transcription of kit, a hallmark of spermatogonial differentiation. Plzf represses both endogenous kit expression and expression of a reporter gene under the control of the kit promoter region. A discrete sequence of the kit promoter, required for Plzf-mediated kit transcriptional repression, is bound by Plzf both in vivo and in vitro. A 3-bp mutation in this Plzf binding site abolishes the responsiveness of the kit promoter to Plzf repression. A significant increase in kit expression is also found in the undifferentiated spermatogonia isolated from Plzf–/– mice. Thus, we suggest that one mechanism by which Plzf maintains the pool of spermatogonial stem cells is through a direct repression of kit expression.
Published ahead of print on 30 July 2007.
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