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Mol. Cell. Biol., 07 1997, 3809-3816, Vol 17, No. 7
D Yean and J Gralla
Promoters need to specify both the timing of transcriptional induction and
the amount of transcript synthesized. In order to explore each of these
effects separately, in vitro assays for the level of active preinitiation
complex formation and for the rate of continuous RNA production were done.
The effects were found to be influenced differently by different promoter
elements. A consensus TATA element had a very strong effect on the rate of
continuous RNA production, whereas two types of activators were important
primarily in forming active transcription preinitiation complexes.
Consensus TATA promoters exhibited high rates of continuous transcription;
they assembled active preinitiation transcription complexes slowly but then
produced transcripts continuously at an approximately fivefold-higher rate.
Initiator-containing TATA-less promoters produced continuous transcripts
slowly. Point mutations in the TATA element led to lower levels of
transcription by reducing the number of preinitiation complexes and
amplifying this reduction by lowering the apparent reinitiation rate. The
results allow understanding of the sequence diversity of promoter elements
in terms of specifying separate controls over the sensitivity of gene
induction and over the strength of the induced promoter.
Copyright © 1997, American Society for Microbiology
Transcription reinitiation rate: a special role for the TATA box
Department of Chemistry & Biochemistry and Molecular Biology Institute, University of California, Los Angeles 90095-1569, USA.
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