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Molecular and Cellular Biology, December 2000, p. 9182-9191, Vol. 20, No. 24
Cell and Molecular Biology
Program1 and Department of Biochemistry
and Molecular Biology,2 Michigan State
University, East Lansing, Michigan 48824
Received 14 April 2000/Returned for modification 28 May
2000/Accepted 2 October 2000
The retinoblastoma protein (RB) represses RNA polymerase III
transcription effectively both in vivo and in vitro. Here we demonstrate that the general transcription factors snRNA-activating protein complex (SNAPc) and TATA binding protein (TBP) are
important for RB repression of human U6 snRNA gene transcription by RNA polymerase III. RB is associated with SNAPc as detected by
both coimmunoprecipitation of endogenous RB with SNAPc and
cofractionation of RB and SNAPc during chromatographic
purification. RB also interacts with two SNAPc subunits,
SNAP43 and SNAP50. TBP or a combination of TBP and SNAPc
restores efficient U6 transcription from RB-treated extracts,
indicating that TBP is also involved in RB regulation. In contrast, the
TBP-containing complex TFIIIB restores adenovirus VAI but not human U6
transcription in RB-treated extracts, suggesting that TFIIIB is
important for RB regulation of tRNA-like genes. These results suggest
that different classes of RNA polymerase III-transcribed genes have
distinct general transcription factor requirements for repression by RB.
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Copyright © 2000, American Society for Microbiology. All rights reserved.
The Retinoblastoma Tumor Suppressor Protein Targets Distinct
General Transcription Factors To Regulate RNA Polymerase III
Gene Expression
*
Corresponding author. Mailing address: Department of
Biochemistry and Molecular Biology, Michigan State University,
East Lansing, MI 48824. Phone: (517) 353-3980. Fax: (517) 353-9334. E-mail: henryrw{at}pilot.msu.edu.
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