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. 1995 Jun 1;14(11):2570-9.
doi: 10.1002/j.1460-2075.1995.tb07255.x.

Poly(dA:dT), a ubiquitous promoter element that stimulates transcription via its intrinsic DNA structure

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Poly(dA:dT), a ubiquitous promoter element that stimulates transcription via its intrinsic DNA structure

V Iyer et al. EMBO J. .

Abstract

Many yeast promoters contain homopolymeric dA:dT sequences that affect nucleosome formation in vitro and are required for wild-type levels of transcription in vivo. Here, we show that poly(dA:dT) is a novel promoter element whose function depends on its intrinsic structure, not its interaction with sequence-specific, DNA-binding proteins. First, poly(dA:dT) stimulates Gcn4-activated transcription in a manner that is length dependent and inversely related to intracellular Gcn4 levels. Second, Datin, the only known poly(dA:dT)-binding protein, behaves as a repressor through poly(dA:dT) sequences. Third, poly(dG:dC), a structurally dissimilar homopolymer that also affects nucleosomes, has transcriptional properties virtually identical to those of poly(dA:dT). Three probes of chromatin structure including HinfI endonuclease cleavage in vivo indicate that poly(dA:dT) increases accessibility of the Gcn4 binding site and adjacent sequences in physiological chromatin. These observations suggest that, by virtue of its intrinsic structure, poly(dA:dT) locally affects nucleosomes and increases the accessibility of transcription factors bound to nearby sequences.

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    1. Nucleic Acids Res. 1979 Apr;6(4):1387-415 - PubMed
    1. Nucleic Acids Res. 1993 Feb 11;21(3):703-11 - PubMed
    1. J Mol Biol. 1980 Jan 25;136(3):309-32 - PubMed
    1. Nature. 1981 Jul 23;292(5821):375-8 - PubMed
    1. Nature. 1981 Jul 23;292(5821):378-80 - PubMed

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