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Molecular and Cellular Biology, April 1999, p. 2835-2845, Vol. 19, No. 4
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
MOT1 Can Activate Basal Transcription In Vitro by
Regulating the Distribution of TATA Binding Protein between
Promoter and Nonpromoter Sites
Tamara A.
Muldrow,1
Allyson M.
Campbell,2
P. Anthony
Weil,2 and
David
T.
Auble1,*
Department of Biochemistry and Molecular
Genetics, University of Virginia Health Science Center,
Charlottesville, Virginia 22908,1 and
Department of Molecular Physiology and Biophysics,
Vanderbilt University School of Medicine, Nashville, Tennessee
37232-06152
Received 10 December 1998/Accepted 13 January 1999
MOT1 is an ATPase which can dissociate TATA binding protein
(TBP)-DNA complexes in a reaction requiring ATP hydrolysis.
Consistent with this observation, MOT1 can repress basal transcription
in vitro. Paradoxically, however, some genes, such as HIS4,
appear to require MOT1 as an activator of transcription in vivo. To
further investigate the function of MOT1 in basal transcription, we
performed in vitro transcription reactions using yeast nuclear extracts depleted of MOT1. Quantitation of MOT1 revealed that it is an abundant protein, with nuclear extracts from wild-type cells containing a molar excess of MOT1 over TBP. Surprisingly, MOT1 can weakly activate basal transcription in vitro. This activation by MOT1 is
detectable with amounts of MOT1 that are approximately stoichiometric to TBP. With amounts of MOT1 similar to those present in
wild-type nuclear extracts, MOT1 behaves as a weak repressor of basal
transcription. These results suggest that MOT1 might activate
transcription via an indirect mechanism in which limiting TBP can be
liberated from nonpromoter sites for use at promoters. In support of
this idea, excess nonpromoter DNA sequesters TBP and represses
transcription, but this effect can be reversed by addition of MOT1.
These results help to reconcile previous in vitro and in vivo results
and expand the repertoire of transcriptional control strategies to
include factor-assisted redistribution of TBP between promoter and
nonpromoter sites.
*
Corresponding author. Mailing address: Department of
Biochemistry and Molecular Genetics, University of Virginia Health
Science Center, Charlottesville, VA 22908. Phone: (804) 243-2629. Fax: (804) 924-5069. E-mail: dta4n{at}virginia.edu.
Molecular and Cellular Biology, April 1999, p. 2835-2845, Vol. 19, No. 4
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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