The HIP1 initiator element plays a role in determining the in vitro requirement of the dihydrofolate reductase gene promoter for the C-terminal domain of RNA polymerase II

A. B. Buermeyer, N. E. Thompson, L. A. Strasheim, R. R. Burgess, P. J. Farnham

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

We examined the ability of purified RNA polymerase (RNAP) II lacking the carboxy-terminal heptapeptide repeat domain (CTD), called RNAP IIB, to transcribe a variety of promoters in HeLa extracts in which endogenous RNAP II activity was inhibited with anti-CTD monoclonal antibodies. Not all promoters were efficiently transcribed by RNAP IIB, and transcription did not correlate with the in vitro strength of the promoter or with the presence of a consensus TATA box. This was best illustrated by the GC-rich, non-TATA box promoters of the bidirectional dihydrofolate reductase (DHFR)-REP-encoding locus. Whereas the REP promoter was transcribed by RNAP IIB, the DHFR promoter remained inactive after addition of RNAP HB to the antibody-inhibited reactions. However, both promoters were efficiently transcribed when purified RNAP with an intact CTD was added. We analyzed a series of promoter deletions to identify which cis elements determine the requirement for the CTD of RNAP II. All of the promoter deletions of both DHFR and REP retained the characteristics of their respective full-length promoters, suggesting that the information necessary to specify the requirement for the CTD is contained within approximately 65 bp near the initiation site. Furthermore, a synthetic minimal promoter of DHFR, consisting of a single binding site for Sp1 and a binding site for the HIP1 initiator cloned into a bacterial vector sequence, required RNAP II with an intact CTD for activity in vitro. Since the synthetic minimal promoter of DHFR and the smallest REP promoter deletion are both activated by Sp1, the differential response in this assay does not result from upstream activators. However, the sequences around the start sites of DHFR and REP are not similar and our data suggest that they bind different proteins. Therefore, we propose that specific initiator elements are important for determination of the requirement of some promoters for the CTD.

Original languageEnglish (US)
Pages (from-to)2250-2259
Number of pages10
JournalMolecular and Cellular Biology
Volume12
Issue number5
StatePublished - May 1992
Externally publishedYes

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Tetrahydrofolate Dehydrogenase
RNA Polymerase II
DNA-Directed RNA Polymerases
Genes
Binding Sites
TATA Box
Terminal Repeat Sequences
In Vitro Techniques
Monoclonal Antibodies
Antibodies
Proteins

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cell Biology

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The HIP1 initiator element plays a role in determining the in vitro requirement of the dihydrofolate reductase gene promoter for the C-terminal domain of RNA polymerase II. / Buermeyer, A. B.; Thompson, N. E.; Strasheim, L. A.; Burgess, R. R.; Farnham, P. J.

In: Molecular and Cellular Biology, Vol. 12, No. 5, 05.1992, p. 2250-2259.

Research output: Contribution to journalArticle

Buermeyer, A. B. ; Thompson, N. E. ; Strasheim, L. A. ; Burgess, R. R. ; Farnham, P. J. / The HIP1 initiator element plays a role in determining the in vitro requirement of the dihydrofolate reductase gene promoter for the C-terminal domain of RNA polymerase II. In: Molecular and Cellular Biology. 1992 ; Vol. 12, No. 5. pp. 2250-2259.
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