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Corepressor-Dependent Silencing of Chromosomal Regions Encoding Neuronal Genes
Victoria V. Lunyak,1Robert Burgess,1*Gratien G. Prefontaine,1Charles Nelson,1Sing-Hoi Sze,2Josh Chenoweth,3Phillip Schwartz,4Pavel A. Pevzner,2Christopher Glass,5Gail Mandel,3Michael G. Rosenfeld1
The molecular mechanisms by which central nervous
system-specific genes are expressed only in the nervous system
and repressedin other tissues remain a central issue in developmental
and regulatorybiology. Here, we report that the zinc-finger
gene-specific repressorelement RE-1 silencing transcription
factor/neuronal restrictedsilencing factor (REST/NRSF) can mediate
extraneuronal restrictionby imposing either active repression via
histone deacetylase recruitmentor long-term gene silencing using a
distinct functional complex.Silencing of neuronal-specific genes
requires the recruitmentof an associated corepressor, CoREST, that
serves as a functionalmolecular beacon for the recruitment of
molecular machinery thatimposes silencing across a chromosomal
interval, including transcriptionalunits that do not themselves
contain REST/NRSF response elements.
1 Howard Hughes Medical Institute (HHMI),
2 Department of Computer Science and Engineering,
School of Medicine, University of California, San Diego, 9500 Gilman
Drive, Room 345, La Jolla, CA 92093-0648, USA.
3 Howard Hughes Medical Institute, Department of
Neurobiology, State University of New York, Stony Brook, NY 11794, USA.
4 Affinity BioReagents, Incorporated, 14818 West 6th
Avenue, Suite 10A, Golden, CO 80401, USA.
5 Department of Cellular and Molecular Medicine,
School of Medicine, University of California, San Diego, La Jolla, CA
92093, USA.
*
Present address: Beckman Institute for Biomedical Research,
Department of Functional Genomics, Temecula, CA 92590, USA.
To whom correspondence should be addressed. E-mail:
mrosenfeld{at}ucsd.edu
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