Home LiteratureArticle Details
PMID: 100614 Published · ppublish English Journal Article

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

Journal of virology ·Vol. 28 ·No. 1 ·1978-10-00 ·Pages 95-105

Chenciner N, Milanesi G

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.

MeSH Terms
Bacillus subtilis/enzymology Bacteriophages/analysis,metabolism DNA Restriction Enzymes/metabolism DNA, Viral/analysis,metabolism DNA-Directed RNA Polymerases/metabolism Nucleic Acid Hybridization RNA, Viral/biosynthesis Templates, Genetic Transcription, Genetic
Chemicals
DNA, Viral RNA, Viral DNA-Directed RNA Polymerases DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Chenciner N
Milanesi G
References (14)
14 references, click to expand
  1. Detection of specific sequences among DNA fragments separated by gel electrophoresis.
    J Mol Biol. 1975 Nov 5;98(3):503-17 PMID: 1195397
  2. RNA polymerase binding sites in lambdaplac5 DNA.
    Proc Natl Acad Sci U S A. 1977 Nov;74(11):4914-8 PMID: 270725
  3. Interaction of RNA polymerase with promoters from bacteriophage fd.
    Eur J Biochem. 1977 Mar 15;74(1):107-13 PMID: 300680
  4. RNA polymerase from Bacillus subtilis: isolation of core and holo enzyme by DNA-cellulose chromatography.
    Nucleic Acids Res. 1977 Mar;4(3):603-23 PMID: 405660
  5. Restriction fragment analysis of the temporal program of bacteriophage SPO1 transcription and its control by phage-modified RNA polymerases.
    Virology. 1977 Dec;83(2):365-79 PMID: 412317
  6. Relationship between competence for transfection and for transformation.
    J Virol. 1968 Jun;2(6):587-93 PMID: 4177104
  7. Asymmetric transcription of SPP1 in vivo.
    Mol Gen Genet. 1973 Jul 31;124(1):57-63 PMID: 4200375
  8. In vivo and in vitro transcription of SPP1 DNA by host RNA polymerase.
    J Virol. 1974 Dec;14(6):1613-4 PMID: 4214951
  9. Transcription after bacteriophage SPP1 infection in Bacillus subtilis.
    J Virol. 1972 Aug;10(2):187-92 PMID: 4627475
  10. A new phage of Bacillus subtilis with infectious DNA having separable strands.
    J Mol Biol. 1968 Jul 28;35(2):347-56 PMID: 5000316
  11. The ribonuclease activity of crystallized pancreatic deoxyribonuclease.
    Anal Biochem. 1966 Feb;14(2):269-77 PMID: 5939865
  12. Gene expression of bacteriophage SPPI. I. Phage directed protein synthesis.
    Mol Gen Genet. 1975 Dec 23;142(1):45-55 PMID: 814401
  13. Gene expression of bacteriophage SPP1. II. Regulatory aspects.
    Mol Gen Genet. 1975 Dec 23;142(1):57-66 PMID: 814402
  14. Hybridization of the in vitro products of bacteriop&hage T7 RNA polymerase to restriction fragments of T7 DNA.
    Virology. 1977 Oct 15;82(2):288-98 PMID: 919342
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1978-10-00
Pages
95-105
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC354251
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]