Literature DB >> 7797075

Activation of the TFIID-TFIIA complex with HMG-2.

B M Shykind1, J Kim, P A Sharp.   

Abstract

The nonhistone chromosomal protein HMG-2 was identified as a factor necessary for activation in a defined transcription reaction in vitro containing RNA polymerase II and purified factors. Activation occurred on all promoters assayed except that of the immunoglobulin IgH gene. TFIIA was required for stimulated levels of transcription. The activation process depended on the presence of TAFs in the TFIID complex and generated a preinitiation complex from which TFIIB dissociated more slowly. However, titration of TFIIB over three orders of magnitude did not obviate the requirement of activator and HMG-2 to achieve stimulated levels of transcription. Analysis of the activated reaction identified the TFIID-TFIIA complex as the first stage of modification during activation. These results suggest that activation can occur solely in the presence of the basal factors, activator protein, and an "architectural" HMG factor, which probably stabilizes an activated conformation of the TFIID-TFIIA-promoter complex.

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Year:  1995        PMID: 7797075     DOI: 10.1101/gad.9.11.1354

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  58 in total

1.  High-mobility-group proteins NHP6A and NHP6B participate in activation of the RNA polymerase III SNR6 gene.

Authors:  S Lopez; M Livingstone-Zatchej; S Jourdain; F Thoma; A Sentenac; M C Marsolier
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

2.  Characterization and functional analysis of Arabidopsis TFIIA reveal that the evolutionarily unconserved region of the large subunit has a transcription activation domain.

Authors:  Y F Li; J Le Gourierrec; M Torki; Y J Kim; F Guerineau; D X Zhou
Journal:  Plant Mol Biol       Date:  1999-02       Impact factor: 4.076

3.  Solution structure of the HMG protein NHP6A and its interaction with DNA reveals the structural determinants for non-sequence-specific binding.

Authors:  F H Allain; Y M Yen; J E Masse; P Schultze; T Dieckmann; R C Johnson; J Feigon
Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

4.  A new screen for protein interactions reveals that the Saccharomyces cerevisiae high mobility group proteins Nhp6A/B are involved in the regulation of the GAL1 promoter.

Authors:  H Laser; C Bongards; J Schüller; S Heck; N Johnsson; N Lehming
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

Review 5.  Multi-protein complexes in eukaryotic gene transcription.

Authors:  Ernest Martinez
Journal:  Plant Mol Biol       Date:  2002-12       Impact factor: 4.076

6.  Separation of the transcriptional coactivator and antirepression functions of transcription factor IIA.

Authors:  D MA; I Olave; A Merino; D Reinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-25       Impact factor: 11.205

7.  TFIIA plays a role in the response to oxidative stress.

Authors:  Susan M Kraemer; David A Goldstrohm; Ann Berger; Susan Hankey; Sherry A Rovinsky; W Scott Moye-Rowley; Laurie A Stargell
Journal:  Eukaryot Cell       Date:  2006-07

8.  Alleviation of histone H1-mediated transcriptional repression and chromatin compaction by the acidic activation region in chromosomal protein HMG-14.

Authors:  H F Ding; M Bustin; U Hansen
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

Review 9.  Molecular genetics of the RNA polymerase II general transcriptional machinery.

Authors:  M Hampsey
Journal:  Microbiol Mol Biol Rev       Date:  1998-06       Impact factor: 11.056

10.  Isolation of cDNAs encoding novel transcription coactivators p52 and p75 reveals an alternate regulatory mechanism of transcriptional activation.

Authors:  H Ge; Y Si; R G Roeder
Journal:  EMBO J       Date:  1998-11-16       Impact factor: 11.598

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