Abstract
Promoters containing Sp1 binding sites and an initiator element but lacking a TATA box direct high levels of accurate transcription initiation by using a mechanism that requires the TATA-binding protein (TBP). We have begun to address the role of TBP during transcription from Sp1-initiator promoters by varying the nucleotide sequence between -14 and -33 relative to the start site. With each of several promoters containing different upstream sequences, we detected accurate transcription both in vitro and in vivo, but the promoter strengths varied widely, particularly with the in vitro assay. The variable promoter activities correlated with, but were not proportional to, the abilities of the upstream sequences to function as TATA boxes, as assessed by multiple criteria. These results confirm that accurate transcription can proceed in the presence of an initiator, regardless of the sequence present in the -30 region. However, the results reveal a role for this upstream region, most consistent with a model in which initiator-mediated transcription requires binding of TBP to the upstream DNA in the absence of a specific recognition sequence. Moreover, in vivo it appears that the promoter strength is modulated less severely by altering the -30 sequence, consistent with a previous suggestion that TBP is not rate limiting in vivo for TATA-less promoters. Taken together, these results suggest that variations in the structure of a core promoter might alter the rate-limiting step for transcription initiation and thereby alter the potential modes of transcriptional regulation, without severely changing the pathway used to assemble a functional preinitiation complex.
MeSH Terms
Base Sequence
DNA/metabolism
DNA-Binding Proteins/metabolism
Genetic Variation
Humans
Molecular Sequence Data
Plasmids
Promoter Regions, Genetic
TATA-Box Binding Protein
Transcription Factors/metabolism
Transcription, Genetic
Transfection
Chemicals
DNA-Binding Proteins
TATA-Box Binding Protein
Transcription Factors
DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zenzie-Gregory B
Howard Hughes Medical Institute, UCLA School of Medicine 90024-1662.
Khachi A
Garraway I P
Smale S T
References (24)
24 references, click to expand
-
Transcription of herpes simplex virus tk sequences under the control of wild-type and mutant human RNA polymerase I promoters.
Mol Cell Biol. 1985 Feb;5(2):352-62
PMID: 2983190
-
Holo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter.
Genes Dev. 1992 Oct;6(10):1964-74
PMID: 1398073
-
The "initiator" as a transcription control element.
Cell. 1989 Apr 7;57(1):103-13
PMID: 2467742
-
Yeast TATA-binding protein TFIID binds to TATA elements with both consensus and nonconsensus DNA sequences.
Proc Natl Acad Sci U S A. 1989 Aug;86(15):5718-22
PMID: 2569738
-
Transcription initiation from the dihydrofolate reductase promoter is positioned by HIP1 binding at the initiation site.
Mol Cell Biol. 1990 Feb;10(2):653-61
PMID: 2300058
-
Functional dissection of a mouse ribosomal protein promoter: significance of the polypyrimidine initiator and an element in the TATA-box region.
Proc Natl Acad Sci U S A. 1990 Feb;87(4):1526-30
PMID: 2304915
-
Transcription initiated by RNA polymerase II and purified transcription factors from liver. A complex set of promoter sequences governs formation of the initial complex.
J Biol Chem. 1990 May 5;265(13):7564-9
PMID: 2159003
-
Transcriptional activation by Sp1 as directed through TATA or initiator: specific requirement for mammalian transcription factor IID.
Proc Natl Acad Sci U S A. 1990 Jun;87(12):4509-13
PMID: 2141169
-
Cloning of a transcriptionally active human TATA binding factor.
Science. 1990 Jun 29;248(4963):1646-50
PMID: 2194289
-
Mechanism of transcriptional activation by Sp1: evidence for coactivators.
Cell. 1990 Jun 29;61(7):1187-97
PMID: 2194667
-
RNA polymerase B (II) and general transcription factors.
Annu Rev Biochem. 1990;59:711-54
PMID: 2197989
-
Initiation of transcription of the erythroid promoter of the porphobilinogen deaminase gene is regulated by a cis-acting sequence around the cap site.
Nucleic Acids Res. 1990 Nov 25;18(22):6509-15
PMID: 2251113
-
Isolation of coactivators associated with the TATA-binding protein that mediate transcriptional activation.
Cell. 1991 Aug 9;66(3):563-76
PMID: 1907890
-
The initiator directs the assembly of a transcription factor IID-dependent transcription complex.
Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):8052-6
PMID: 1896450
-
LyF-1, a transcriptional regulator that interacts with a novel class of promoters for lymphocyte-specific genes.
Mol Cell Biol. 1991 Oct;11(10):5229-43
PMID: 1922043
-
Cooperative interaction of an initiator-binding transcription initiation factor and the helix-loop-helix activator USF.
Nature. 1991 Nov 21;354(6350):245-8
PMID: 1961251
-
TFIID binds in the minor groove of the TATA box.
Cell. 1991 Dec 20;67(6):1231-40
PMID: 1760847
-
Interaction of TFIID in the minor groove of the TATA element.
Cell. 1991 Dec 20;67(6):1241-50
PMID: 1760848
-
Roles of TATA and initiator elements in determining the start site location and direction of RNA polymerase II transcription.
J Biol Chem. 1992 Jan 15;267(2):1391-402
PMID: 1730658
-
Similar mechanisms for transcription initiation mediated through a TATA box or an initiator element.
J Biol Chem. 1992 Feb 5;267(4):2823-30
PMID: 1733976
-
TFIID can be rate limiting in vivo for TATA-containing, but not TATA-lacking, RNA polymerase II promoters.
Genes Dev. 1992 Feb;6(2):304-15
PMID: 1737620
-
The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells.
Cell. 1992 May 15;69(4):685-96
PMID: 1586947
-
Functional binding of the "TATA" box binding component of transcription factor TFIID to the -30 region of TATA-less promoters.
Proc Natl Acad Sci U S A. 1992 Jul 1;89(13):5814-8
PMID: 1321424
-
Simian virus 40 major late promoter: a novel tripartite structure that includes intragenic sequences.
Mol Cell Biol. 1988 May;8(5):2021-33
PMID: 2838741