Literature DB >> 1760848

Interaction of TFIID in the minor groove of the TATA element.

D K Lee1, M Horikoshi, R G Roeder.   

Abstract

TFIID binding in the minor groove of DNA at the TATA element was demonstrated by methylation interference and hydroxyl radical footprinting assays, and by binding studies with thymine analog substituted oligonucleotides. These results provide an explanation for TFIID-dependent DNA bending at the TATA element. TFIID binding shows phosphate contacts with the same residues that were found to be essential for TFIID interactions by methylation and thymine-specific modification interference assays. Based on previous studies implicating residues conserved between the direct repeats in DNA binding, as well as models of prokaryotic DNA binding proteins, these results also suggest a model in which the direct repeats of TFIID form two basic antiparallel beta ribbon arms that could contact DNA through the minor groove.

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Year:  1991        PMID: 1760848     DOI: 10.1016/0092-8674(91)90300-n

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  58 in total

1.  TFIIA induces conformational changes in TFIID via interactions with the basic repeat.

Authors:  D K Lee; J DeJong; S Hashimoto; M Horikoshi; R G Roeder
Journal:  Mol Cell Biol       Date:  1992-11       Impact factor: 4.272

2.  A bipartite DNA binding domain composed of direct repeats in the TATA box binding factor TFIID.

Authors:  T Yamamoto; M Horikoshi; J Wang; S Hasegawa; P A Weil; R G Roeder
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-01       Impact factor: 11.205

3.  The host factor polyhedrin promoter binding protein (PPBP) is involved in transcription from the baculovirus polyhedrin gene promoter.

Authors:  S Ghosh; A Jain; B Mukherjee; S Habib; S E Hasnain
Journal:  J Virol       Date:  1998-09       Impact factor: 5.103

Review 4.  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

5.  Point mutations 5' to the tRNA selenocysteine TATA box alter RNA polymerase III transcription by affecting the binding of TBP.

Authors:  E Myslinski; C Schuster; J Huet; A Sentenac; A Krol; P Carbon
Journal:  Nucleic Acids Res       Date:  1993-12-25       Impact factor: 16.971

6.  Interaction between a novel F9-specific factor and octamer-binding proteins is required for cell-type-restricted activity of the fibroblast growth factor 4 enhancer.

Authors:  L Dailey; H Yuan; C Basilico
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

7.  An inverted TATA box directs downstream transcription of the bone sialoprotein gene.

Authors:  J J Li; R H Kim; J Sodek
Journal:  Biochem J       Date:  1995-08-15       Impact factor: 3.857

8.  Effect of the non-conserved N-terminus on the DNA binding activity of the yeast TATA binding protein.

Authors:  R Kuddus; M C Schmidt
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

9.  Equivalent mutations in the two repeats of yeast TATA-binding protein confer distinct TATA recognition specificities.

Authors:  K M Arndt; C R Wobbe; S Ricupero-Hovasse; K Struhl; F Winston
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

10.  Mechanism of initiator-mediated transcription: evidence for a functional interaction between the TATA-binding protein and DNA in the absence of a specific recognition sequence.

Authors:  B Zenzie-Gregory; A Khachi; I P Garraway; S T Smale
Journal:  Mol Cell Biol       Date:  1993-07       Impact factor: 4.272

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