Literature DB >> 8211143

Regional codon randomization: defining a TATA-binding protein surface required for RNA polymerase III transcription.

B P Cormack1, K Struhl.   

Abstract

The TATA-binding protein (TBP) is required for transcription by all three nuclear RNA polymerases. TBP was subjected to regional codon randomization, a codon-based mutagenesis method that generates complex yet compact protein libraries. Analysis of 186 temperature-sensitive TBP mutants yielded 65 specifically defective in transcription by RNA polymerase III (Pol III). These mutants map to a limited TBP surface that may interact with Tds4, a component of the Pol III transcription factor TFIIIB. Strains that contain the Pol III-defective derivatives have increased amounts of messenger RNA, which suggests that competition among TBP-interacting factors for limiting quantities of TBP determines the ratio of Pol II and Pol III transcription in vivo.

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Year:  1993        PMID: 8211143     DOI: 10.1126/science.8211143

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  36 in total

1.  Qsr1p, a 60S ribosomal subunit protein, is required for joining of 40S and 60S subunits.

Authors:  D P Eisinger; F A Dick; B L Trumpower
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

Review 2.  Comparison of the RNA polymerase III transcription machinery in Schizosaccharomyces pombe, Saccharomyces cerevisiae and human.

Authors:  Y Huang; R J Maraia
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

3.  A severely defective TATA-binding protein-TFIIB interaction does not preclude transcriptional activation in vivo.

Authors:  M Lee; K Struhl
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

4.  Codon-based mutagenesis using dimer-phosphoramidites.

Authors:  P Neuner; R Cortese; P Monaci
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

5.  Polymerase (Pol) III TATA box-binding protein (TBP)-associated factor Brf binds to a surface on TBP also required for activated Pol II transcription.

Authors:  Y Shen; G A Kassavetis; G O Bryant; A J Berk
Journal:  Mol Cell Biol       Date:  1998-03       Impact factor: 4.272

6.  Different positioning of the ligand-binding domain helix 12 and the F domain of the estrogen receptor accounts for functional differences between agonists and antagonists.

Authors:  M Nichols; J M Rientjes; A F Stewart
Journal:  EMBO J       Date:  1998-02-02       Impact factor: 11.598

7.  Using altered specificity Oct-1 and Oct-2 mutants to analyze the regulation of immunoglobulin gene transcription.

Authors:  P C Shah; E Bertolino; H Singh
Journal:  EMBO J       Date:  1997-12-01       Impact factor: 11.598

8.  Molding a peptide into an RNA site by in vivo peptide evolution.

Authors:  K Harada; S S Martin; R Tan; A D Frankel
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

9.  A differential response of wild type and mutant promoters to TFIIIB70 overexpression in vivo and in vitro.

Authors:  I Sethy-Coraci; R D Moir; A López-de-León; I M Willis
Journal:  Nucleic Acids Res       Date:  1998-05-15       Impact factor: 16.971

10.  Interaction between TBP and Condensin Drives the Organization and Faithful Segregation of Mitotic Chromosomes.

Authors:  Osamu Iwasaki; Hideki Tanizawa; Kyoung-Dong Kim; Yuhki Yokoyama; Christopher J Corcoran; Atsunari Tanaka; Emmanuel Skordalakes; Louise C Showe; Ken-Ichi Noma
Journal:  Mol Cell       Date:  2015-08-06       Impact factor: 17.970

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