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PMID: 3081264 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Inefficient translation initiation causes premature transcription termination in the lacZ gene.

Cell ·Vol. 44 ·No. 5 ·1986-03-14 ·Pages 711-8

Stanssens P, Remaut E, Fiers W

Abstract

Expression plasmids containing the E. coli lacZ coding region preceded by a set of different ribosome-binding sites and put under transcriptional control of the leftward promoter of phage lambda (PL) were used to study the synthesis of lacZ mRNA. In a normal host the steady state level of full-length lacZ mRNA varied 100-fold with the different synthesis levels of beta-galactosidase, whereas in a host expressing the antitermination protein N of phage lambda, all vectors synthesized the same amount of full-length lacZ mRNA, while maintaining the differences in beta-galactosidase expression. We present evidence for a causal relationship between the rate of ribosome loading and the continuation of transcription across the lacZ gene. We suggest that extended spacing between the RNA polymerase and the elongating ribosome causes transcriptional polarity by increasing the extent of premature termination. The conditional character of the termination event can best be explained by invoking termination factor Rho.

MeSH Terms
Galactosidases/genetics Gene Expression Regulation Lac Operon Plasmids Promoter Regions, Genetic Protein Biosynthesis RNA, Messenger/genetics,metabolism Ribosomes/metabolism Transcription, Genetic beta-Galactosidase/genetics
Chemicals
RNA, Messenger Galactosidases beta-Galactosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Stanssens P
Remaut E
Fiers W
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1986-03-14
Pages
711-8
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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