NDLI: Artificial regulation of gene expression in Escherichia coli by RNase P.

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Artificial regulation of gene expression in Escherichia coli by RNase P.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Altman, S. Guerrier-takada, C. Li, Y.
Description	Author Affiliation: Guerrier-Takada C ( Department of Biology, Yale University, New Haven, CT 06520, USA.);
Abstract	Plasmids encoding various external guide sequences (EGSs) were constructed and inserted into Escherichia coli. In strains harboring the appropriate plasmids, the expression of fully induced beta-galactosidase and alkaline phosphatase activity was reduced by more than 50%, while no reduction in such activity was observed in strains with non-specific EGSs. The inhibition of gene expression was virtually abolished at restrictive temperatures in strains that were temperature-sensitive for RNase P (EC 3.1.26.5). Northern blot analysis showed that the steady-state copy number of EGS RNAs was several hundred per cell in vivo. A plasmid that contained a gene for M1 RNA covalently linked to a specific EGS reduced the level of expression of a suppressor tRNA that was encoded by a separate plasmid. Similar methods can be used to regulate gene expression in E. coli and to mimic the properties of cold-sensitive mutants.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	24
Volume Number	92
Language	English
Publisher	National Academy of Sciences
Publisher Date	1995-12-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Endoribonucleases Physiology Escherichia Coli Proteins Escherichia Coli Genetics Gene Expression Regulation, Bacterial RNA, Catalytic Enzymology Molecular Sequence Data Oligoribonucleotides Chemistry RNA, Antisense RNA, Bacterial RNA, Messenger Ribonuclease P Temperature Research Support, U.S. Gov't, P.H.S. Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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