Literature DB >> 827446

Transcription in vitro of phi29 DNA and EcoRI fragments by Bacillus subtilis RNA polymerase.

M R Inciarte, E Viñuela, M Salas.   

Abstract

EcoRI fragments A, B and C produced from linear phi29 DNA, but not D or E fragments, are transcribed by purified Bacillus subtilis RNA polymerase. The transcription of fragments A and C is initiated preferentially with GTP and to a lesser extent with ATP; the reverse happens in the case of fragment B. The dinucleotides GpU and GpA respectively, compete specifically with the incorporation of [gamma-32P]GTP directed by fragments A and C. The RNA synthesized in vitro by purified B. subtilis RNA polymerase is highly asymmetric. Most of the RNA synthesis directed by fragments A and C is early RNA. However, most of the RNA produced by fragment B is anti-late-RNA. Addition of crude extracts inhibit the transcription of fragment B but not that of fragments A and C.

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Year:  1976        PMID: 827446     DOI: 10.1111/j.1432-1033.1976.tb11091.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  8 in total

1.  Structural and functional analysis of temperature-sensitive mutants of the phage phi 29 DNA polymerase.

Authors:  M A Blasco; L Blanco; E Parés; M Salas; A Bernad
Journal:  Nucleic Acids Res       Date:  1990-08-25       Impact factor: 16.971

2.  A DNA binding motif coordinating synthesis and degradation in proofreading DNA polymerases.

Authors:  V Truniger; J M Lázaro; M Salas; L Blanco
Journal:  EMBO J       Date:  1996-07-01       Impact factor: 11.598

3.  The highly conserved amino acid sequence motif Tyr-Gly-Asp-Thr-Asp-Ser in alpha-like DNA polymerases is required by phage phi 29 DNA polymerase for protein-primed initiation and polymerization.

Authors:  A Bernad; J M Lázaro; M Salas; L Blanco
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

4.  Nucleotide sequences at the termini of phi 29 DNA.

Authors:  H Yoshikawa; T Friedmann; J Ito
Journal:  Proc Natl Acad Sci U S A       Date:  1981-03       Impact factor: 11.205

5.  Primer-terminus stabilization at the 3'-5' exonuclease active site of phi29 DNA polymerase. Involvement of two amino acid residues highly conserved in proofreading DNA polymerases.

Authors:  M de Vega; J M Lazaro; M Salas; L Blanco
Journal:  EMBO J       Date:  1996-03-01       Impact factor: 11.598

6.  In vitro synthesis of late bacteriophage phi 29 RNA.

Authors:  R D Holder; H R Whiteley
Journal:  J Virol       Date:  1983-06       Impact factor: 5.103

7.  Site-directed mutagenesis at the Exo III motif of phi 29 DNA polymerase; overlapping structural domains for the 3'-5' exonuclease and strand-displacement activities.

Authors:  M S Soengas; J A Esteban; J M Lázaro; A Bernad; M A Blasco; M Salas; L Blanco
Journal:  EMBO J       Date:  1992-11       Impact factor: 11.598

8.  Functional characterization of highly processive protein-primed DNA polymerases from phages Nf and GA-1, endowed with a potent strand displacement capacity.

Authors:  Elisa Longás; Miguel de Vega; José M Lázaro; Margarita Salas
Journal:  Nucleic Acids Res       Date:  2006-10-28       Impact factor: 16.971

  8 in total

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