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PMID: 6389256 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Identification and characterization of the alc gene product of bacteriophage T4.

Genetics ·Vol. 108 ·No. 2 ·1984-10-00 ·Pages 291-304

Kutter E, Drivdahl R, Rand K

Abstract

Bacteriophage T4 infection rapidly and almost completely inhibits transcription of host and other phage DNAs. Two processes have been implicated to date in this inhibition: (1) ADP ribosylation of the alpha subunits of the RNA polymerase, involving gpalt (which is injected with the phage DNA) and, later, gpmod; and (2) the action of the T4 alc/unf gene product, synthesized immediately after infection. The latter unfolds the host genome and also blocks transcription of cytosine-containing DNA. Here, we describe the identification on two-dimensional polyacrylamide gels of gpalc/unf, the more precise mapping of the gene and the identification and analysis of the appropriate DNA sequence from an Unf+ alc mutant.

MeSH Terms
Amino Acid Sequence Base Sequence DNA, Bacterial/metabolism Electrophoresis, Polyacrylamide Gel Escherichia coli/metabolism T-Phages/analysis,genetics Transcription, Genetic Viral Proteins/genetics,isolation & purification
Chemicals
DNA, Bacterial Viral Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kutter E
Drivdahl R
Rand K
References (17)
17 references, click to expand
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1984-10-00
Pages
291-304
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1202406
Subset
IM
Databases
GENBANK
X00365
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