Literature DB >> 2011525

TFIIIA induced DNA bending: effect of low ionic strength electrophoresis buffer conditions.

G P Schroth1, J M Gottesfeld, E M Bradbury.   

Abstract

We have used a circular permutation gel shift assay to show that the 5S gene transcription factor, TFIIIA, induces a bend at the internal promoter of the Xenopus oocyte-type 5S gene. The degree of bending is comparable to what we have previously observed for TFIIIA induced bending of the Xenopus somatic-type gene [Schroth, G.P. et al. (1989) Nature 340, 487-488]. In addition, we show that TFIIIA induced DNA bending is dramatically affected by the ionic conditions used during gel electrophoresis. By modifying the conditions of the electrophoresis, we can detect two distinct conformations for the TFIIIA/DNA complex. In very low ionic strength buffers, the degree of DNA bending in the complex is estimated to be about 25 to 30 degrees, whereas in higher ionic strength buffers it is about 60 to 65 degrees. These data explain the apparent discrepancy between our results and the results of another study in which it was claimed that TFIIIA did not 'substantially' bend DNA [Zweib, C. and Brown, R.S. (1990) Nucleic Acid Res. 18, 583-587]. These results also demonstrate that the TFIIIA/DNA complex has a large degree of conformational flexibility. Both DNA bending and conformational flexibility are structural features which may provide a key insight into the function of TFIIIA as a positive transcription factor.

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Year:  1991        PMID: 2011525      PMCID: PMC333641          DOI: 10.1093/nar/19.3.511

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  41 in total

Review 1.  Zinc fingers and other metal-binding domains. Elements for interactions between macromolecules.

Authors:  J M Berg
Journal:  J Biol Chem       Date:  1990-04-25       Impact factor: 5.157

2.  Association of a 5S gene transcription factor with 5S RNA and altered levels of the factor during cell differentiation.

Authors:  B M Honda; R G Roeder
Journal:  Cell       Date:  1980-11       Impact factor: 41.582

3.  Physical properties and DNA-binding stoichiometry of a 5 S gene-specific transcription factor.

Authors:  J J Bieker; R G Roeder
Journal:  J Biol Chem       Date:  1984-05-25       Impact factor: 5.157

4.  Contact points between a positive transcription factor and the Xenopus 5S RNA gene.

Authors:  S Sakonju; D D Brown
Journal:  Cell       Date:  1982-12       Impact factor: 41.582

5.  The locus of sequence-directed and protein-induced DNA bending.

Authors:  H M Wu; D M Crothers
Journal:  Nature       Date:  1984 Apr 5-11       Impact factor: 49.962

6.  Domains of the positive transcription factor specific for the Xenopus 5S RNA gene.

Authors:  D R Smith; I J Jackson; D D Brown
Journal:  Cell       Date:  1984-06       Impact factor: 41.582

7.  A specific transcription factor that can bind either the 5S RNA gene or 5S RNA.

Authors:  H R Pelham; D D Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

8.  A control region in the center of the 5S RNA gene directs specific initiation of transcription: II. The 3' border of the region.

Authors:  D F Bogenhagen; S Sakonju; D D Brown
Journal:  Cell       Date:  1980-01       Impact factor: 41.582

9.  Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes.

Authors:  J Miller; A D McLachlan; A Klug
Journal:  EMBO J       Date:  1985-06       Impact factor: 11.598

10.  Structural analysis of a triple complex between the histone octamer, a Xenopus gene for 5S RNA and transcription factor IIIA.

Authors:  D Rhodes
Journal:  EMBO J       Date:  1985-12-16       Impact factor: 11.598

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  3 in total

1.  Definition of the binding sites of individual zinc fingers in the transcription factor IIIA-5S RNA gene complex.

Authors:  K R Clemens; X Liao; V Wolf; P E Wright; J M Gottesfeld
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

Review 2.  Use of gel retardation to analyze protein-nucleic acid interactions.

Authors:  D Lane; P Prentki; M Chandler
Journal:  Microbiol Rev       Date:  1992-12

3.  Herpes simplex virus type 1 polypeptide ICP4 bends DNA.

Authors:  R D Everett; J DiDonato; M Elliott; M Muller
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

  3 in total

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