Literature DB >> 100614

Restriction fragment analysis of bacteriophage SPP1 in vitro transcription by host RNA polymerase.

N Chenciner, G Milanesi.   

Abstract

In vitro transcription of SPP1 DNA occurred on only one of the two strands, the same which is predominantly transcribed in SPP1-infected cells. Transcripts were distributed in several size classes. Analysis of elongation kinetics and of size distribution, coupled with hybridization to DNA restriction fragments, showed that some regions of the template have more initiation sites than others; some have none. Some regions were transcribed directly, some were transcribed from initiation sites located in other regions, and one was never transcribed. Several transcription initiation sites on SPP1 DNA are located on EcoRI fragment 1; four to five others are distributed among other fragments. Cutting the DNA with EcoRI did not introduce artifactual initiation sites. In vitro transcription units can be localized and oriented with respect to the EcoRI restriction map of SPP1 DNA.

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Year:  1978        PMID: 100614      PMCID: PMC354251     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  14 in total

1.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

2.  Interaction of RNA polymerase with promoters from bacteriophage fd.

Authors:  P H Seeburg; C Nüsslein; H Schaller
Journal:  Eur J Biochem       Date:  1977-03-15

3.  RNA polymerase binding sites in lambdaplac5 DNA.

Authors:  B B Jones; H Chan; S Rothstein; R D Wells; W S Reznikoff
Journal:  Proc Natl Acad Sci U S A       Date:  1977-11       Impact factor: 11.205

4.  Restriction fragment analysis of the temporal program of bacteriophage SPO1 transcription and its control by phage-modified RNA polymerases.

Authors:  C Talkington; J Pero
Journal:  Virology       Date:  1977-12       Impact factor: 3.616

5.  Asymmetric transcription of SPP1 in vivo.

Authors:  H Esche; H C Spatz
Journal:  Mol Gen Genet       Date:  1973-07-31

6.  In vivo and in vitro transcription of SPP1 DNA by host RNA polymerase.

Authors:  G Milanesi; F Melgara
Journal:  J Virol       Date:  1974-12       Impact factor: 5.103

7.  A new phage of Bacillus subtilis with infectious DNA having separable strands.

Authors:  S Riva; M Polsinelli; A Falaschi
Journal:  J Mol Biol       Date:  1968-07-28       Impact factor: 5.469

8.  Relationship between competence for transfection and for transformation.

Authors:  S Riva; M Polsinelli
Journal:  J Virol       Date:  1968-06       Impact factor: 5.103

9.  RNA polymerase from Bacillus subtilis: isolation of core and holo enzyme by DNA-cellulose chromatography.

Authors:  P Plevan; A M Albertini; A Galizzi; A Adamoli; G Mastromei; S Riva; G Cassani
Journal:  Nucleic Acids Res       Date:  1977-03       Impact factor: 16.971

10.  Transcription after bacteriophage SPP1 infection in Bacillus subtilis.

Authors:  G Milanesi; G Cassani
Journal:  J Virol       Date:  1972-08       Impact factor: 5.103

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  4 in total

1.  Transcription of nucleosomal DNA in SV40 minichromosomes by eukaryotic and prokaryotic RNA polymerases.

Authors:  G Meneguzzi; N Chenciner; G Milanesi
Journal:  Nucleic Acids Res       Date:  1979-06-25       Impact factor: 16.971

2.  Promoter sites in the genome of B. subtilis phage SPP1.

Authors:  D Stüber; G Morelli; H Bujard; M A Montenegro; T A Trautner
Journal:  Mol Gen Genet       Date:  1981

3.  Bacteriophage SPP1 polypeptides synthesized in infected minicells and in vitro.

Authors:  G Mertens; E Amann; J N Reeve
Journal:  Mol Gen Genet       Date:  1979

4.  The Revisited Genome of Bacillus subtilis Bacteriophage SPP1.

Authors:  Lia M Godinho; Mehdi El Sadek Fadel; Céline Monniot; Lina Jakutyte; Isabelle Auzat; Audrey Labarde; Karima Djacem; Leonor Oliveira; Rut Carballido-Lopez; Silvia Ayora; Paulo Tavares
Journal:  Viruses       Date:  2018-12-11       Impact factor: 5.048

  4 in total

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