Literature DB >> 9632765

Xenopus TFIIIA gene transcription is dependent on cis-element positioning and chromatin structure.

S L Pfaff1, W L Taylor.   

Abstract

The Xenopus TFIIIA gene is transcribed very efficiently in oocytes. In addition to a TATA element at -30, we show that from -425 to +7 the TFIIIA gene contains only two positive cis elements centered at -267 (element 1) and -230 (element 2). This arrangement of the cis elements in the TFIIIA gene is striking because these two elements are positioned very close to each other yet separated from the TATA element by approximately 190 nucleotides. We show that the 190-nucleotide spacing between the TATA element and the upstream cis elements (elements 1 and 2) is critical for efficient transcription of the gene in oocytes and that a nucleosome is positioned in this intervening region. This nucleosome may act positively on TFIIIA transcription in oocytes by placing transcription factors bound at elements 1 and 2 in a favorable position relative to the transcription complex at the TATA element.

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Year:  1998        PMID: 9632765      PMCID: PMC108965          DOI: 10.1128/MCB.18.7.3811

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  41 in total

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Authors:  S L Pfaff; R K Hall; G C Hart; W L Taylor
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Authors:  R K Hall; W L Taylor
Journal:  Mol Cell Biol       Date:  1989-11       Impact factor: 4.272

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Authors:  T Perlmann; O Wrange
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

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Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

10.  Nucleosomes are positioned with base pair precision adjacent to the alpha 2 operator in Saccharomyces cerevisiae.

Authors:  M Shimizu; S Y Roth; C Szent-Gyorgyi; R T Simpson
Journal:  EMBO J       Date:  1991-10       Impact factor: 11.598

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4.  Nucleosome structure of the yeast CHA1 promoter: analysis of activation-dependent chromatin remodeling of an RNA-polymerase-II-transcribed gene in TBP and RNA pol II mutants defective in vivo in response to acidic activators.

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