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Molecular and Cellular Biology, August 1999, p. 5548-5556, Vol. 19, No. 8
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Human Transcription Factor hTAFII150
(CIF150) Is Involved in Transcriptional Regulation of Cell Cycle
Progression
Jay
Martin,
Robert
Halenbeck, and
Jörg
Kaufmann*
Chiron Corporation, Chiron Technologies,
Emeryville, California 94608
Received 2 February 1999/Returned for modification 15 March
1999/Accepted 25 May 1999
Here we present evidence that CIF150 (hTAFII150), the
human homolog of Drosophila TAFII150, plays an
important and selective role in establishing gene expression patterns
necessary for progression through the cell cycle. Gel filtration
experiments demonstrate that CIF150 (hTAFII150) seems to be
less tightly associated with human transcription factor IID than
hTAFII130 is associated with hTAFII250. The
transient functional knockout of CIF150 (hTAFII150) protein
led to cell cycle arrest at the G2/M transition in
mammalian cell lines. PCR display analysis with the RNA derived from
CIF150-depleted cells indicated that CIF150 (hTAFII150) is
required for the transcription of only a subset of RNA polymerase II
genes. CIF150 (hTAFII150) directly stimulated cyclin B1 and
cyclin A transcription in cotransfection assays and in vitro assays,
suggesting that the expression of these genes is dependent on CIF150
(hTAFII150) function. We defined a CIF150
(hTAFII150) consensus binding site and demonstrated that a
CIF150-responsive cis element is present in the cyclin B1
core promoter. These results suggest that one function of CIF150
(hTAFII150) is to select specific RNA polymerase II core
promoter elements involved in cell cycle progression.
*
Corresponding author. Mailing address: Chiron
Corporation, Chiron Technologies, 4560 Horton St., Emeryville, CA
94608. Phone: (510) 923-6946. Fax: (510) 923-5550. E-mail:
Joerg_Kaufmann{at}chiron.com.
Molecular and Cellular Biology, August 1999, p. 5548-5556, Vol. 19, No. 8
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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