Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes

Bidnenko, E. M. ; Akhverdyan, V. Z. ; Krylov, V. N.
Springer
Published 2000
ISSN:
1608-3369
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Notes:
Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297320843902976
autor Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
autorsonst Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
book_url http://dx.doi.org/10.1023/A:1009087811647
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM198719205
iqvoc_descriptor_title iqvoc_00000708:Analysis
issn 1608-3369
journal_name Russian journal of genetics
materialart 1
notes Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
package_name Springer
publikationsjahr_anzeige 2000
publikationsjahr_facette 2000
publikationsjahr_intervall 7999:2000-2004
publikationsjahr_sort 2000
publisher Springer
reference 36 (2000), S. 1454-1457
search_space articles
shingle_author_1 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
shingle_author_2 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
shingle_author_3 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
shingle_author_4 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
shingle_catch_all_1 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
1608-3369
16083369
Springer
shingle_catch_all_2 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
1608-3369
16083369
Springer
shingle_catch_all_3 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
1608-3369
16083369
Springer
shingle_catch_all_4 Bidnenko, E. M.
Akhverdyan, V. Z.
Krylov, V. N.
Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
Abstract At nonpermissive temperature (42°C) thets47 mutation causes substantial abnormalities in the late phase of the phage intracellular development. In these conditions DNA of the D3112 phage is detected both in a free form and integrated into bacterial chromosome. The transcription kinetics in the ts47 mutant at 42°C was indistinguishable from that typical to other early gene mutants (A, B, and C): specifically, the preservation of the first transcription peak along with low activity of late transcription were observed. Similarly to the C gene, the ts47 mutation-carrying locus is involved in regulating the transcription of the D3112 transposable phage late genes. It is suggested that the mechanism underlying the action of thets47 mutation differs from that of the C gene product. One of the possible explanations is based on the fact that the product of the ts47 locus affects the activity of cellular RNA polymerase via providing more effective recognition of the phage promoters by the RNA polymerase modified with the phage protein C.
1608-3369
16083369
Springer
shingle_title_1 Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
shingle_title_2 Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
shingle_title_3 Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
shingle_title_4 Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
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source_archive Springer Online Journal Archives 1860-2000
timestamp 2024-05-06T10:06:08Z
titel Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
titel_suche Analysis of the Phenotypic Effect of the ts47 Mutation of the Pseudomonas aeruginosa Transposable Phage D3112 on the Expression of Late Phage Genes
topic W
uid nat_lic_papers_NLM198719205