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Literature DB >> 4566439

Asymmetric transcription of bacteriophage Mu-1.

Abstract

The deoxyribonucleic acid (DNA) of bacteriophage Mu-1 can be separated into its complementary strands by poly(U,G) binding and equilibrium centrifugation. DNA-ribonucleic acid (RNA) hybridizations in liquid show that more than 98% of "early" phage-specific RNA and over 96% of "late" messenger species bind to the heavy [poly(U,G)-binding] strand of Mu-1 DNA. A small (1.45%) but significant amount of late RNA binds to the light strand. The significance of this RNA fraction is discussed in connection with the peculiar structure of denatured and reannealed Mu-1 DNA.

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Year: 1972 PMID： 4566439 PMCID： PMC356602

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

6 in total

1. BACTERIOPHAGE-INDUCED MUTATION IN ESCHERICHIA COLI.

Authors: A L TAYLOR
Journal: Proc Natl Acad Sci U S A Date: 1963-12 Impact factor: 11.205

2. Synthesis and turnover of phage messenger RNA in E. coli infected with bacteriophage T4 in the presence of chloromycetin.

Authors: K OKAMOTO; Y SUGINO; M NOMURA
Journal: J Mol Biol Date: 1962-11 Impact factor: 5.469

3. A mutation which creates a new site for the re-initiation of polypeptide synthesis in the z gene of the lac operon of Escherichia coli.

Authors: T Grodzicker; D Zipser
Journal: J Mol Biol Date: 1968-12 Impact factor: 5.469

20 in total

9. Mechanism of phage Mu-1 integration: nalidixic acid treatment causes clustering of Mu-1-induced mutations near replication origin.

Authors: L Paolozzi; R Jucker; E Calef
Journal: Proc Natl Acad Sci U S A Date: 1978-10 Impact factor: 11.205

10. Nucleotide sequence of the immunity region of bacteriophage Mu.

Authors: H Priess; D Kamp; R Kahmann; B Bräuer; H Delius
Journal: Mol Gen Genet Date: 1982

Asymmetric transcription of bacteriophage Mu-1.

1. BACTERIOPHAGE-INDUCED MUTATION IN ESCHERICHIA COLI.

2. Synthesis and turnover of phage messenger RNA in E. coli infected with bacteriophage T4 in the presence of chloromycetin.

3. A mutation which creates a new site for the re-initiation of polypeptide synthesis in the z gene of the lac operon of Escherichia coli.

Review 4. Initiation and patterns of transcription during phage development.

5. Transcription of complementary strands of phage lambda-DNA in vivo and in vitro.

6. Electron microscopic evidence for linear insertion of bacteriophage MU-1 in lysogenic bacteria.

1. Origin and binding specificity of protein(s) coded for by Mu prophages.

2. Characterization of the inhomogeneous DNA in virions of bacteriophage Mu by DNA reannealing kinetics.

3. Characterization of the C operon transcript of bacteriophage Mu.

4. Early events in the replication of Mu prophage DNA.

5. On the control of transcription of bacteriophage Mu.

6. Transcription of bacteriophage mu. An analysis of the transcription pattern in the early phase of phage development.

7. Sensitivity of bacteriophage Mu-1 development to rifampicin and streptolydigin.

8. In vitro constructed plasmids containing both ends of bacteriophage Mu DNA express phage functions.

9. Mechanism of phage Mu-1 integration: nalidixic acid treatment causes clustering of Mu-1-induced mutations near replication origin.

10. Nucleotide sequence of the immunity region of bacteriophage Mu.