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PMID: 6454004 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Bacteriophage phi X174-specific mRNA synthesis in cells deficient in termination factor rho activity.

Journal of virology ·Vol. 38 ·No. 1 ·1981-04-00 ·Pages 198-207

Hayashi MN, Hayashi M, Imai M

Abstract

A previous report (Hayashi et al., Proc. Natl. Acad. Sci. U.S.A. 73:3519-3523, 1976) indicated that in vivo bacteriophage phi X174 mRNA's terminate after genes J, F, G, and H. However, termination at these sites is not stringent. To determine whether termination of phi X174 transcription depends on rho factor activity, we introduced a temperature-sensitive rho mutation (nitA) into a phi X174-sensitive host cell line and determined termination sites in wild-type and nitA cells. We found that (i) normal phi X174 terminators were recognized in phi X174-infected nitA cells, (ii) the rho mutation relieved polar effects caused by nonsense mutations in the phage genome or by chloramphenicol treatment of the host cells, and (iii) polarity was not caused by premature termination of transcription at the site of the polar mutation. RNA synthesis continued beyond the site to the first rho-sensitive site.

MeSH Terms
Bacteriophage phi X 174/genetics Chloramphenicol/pharmacology Mutation RNA, Messenger/biosynthesis RNA, Viral/biosynthesis Rho Factor/genetics Transcription Factors/genetics Transcription, Genetic
Chemicals
RNA, Messenger RNA, Viral Rho Factor Transcription Factors Chloramphenicol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hayashi M N
Hayashi M
Imai M
References (30)
30 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1981-04-00
Pages
198-207
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC171140
Subset
IM
Grants
NIGMS NIH HHS · GM 12934 · United States
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