Home LiteratureArticle Details
PMID: 9933592 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Polyadenylation promotes degradation of 3'-structured RNA by the Escherichia coli mRNA degradosome in vitro.

The Journal of biological chemistry ·Vol. 274 ·No. 7 ·1999-02-12 ·Pages 4009-16

Blum E, Carpousis AJ, Higgins CF

Abstract

Polyadenylation contributes to the destabilization of bacterial mRNA. We have investigated the role of polyadenylation in the degradation of RNA by the purified Escherichia coli degradosome in vitro. RNA molecules with 3'-ends incorporated into a stable stem-loop structure could not readily be degraded by purified polynucleotide phosphorylase or by the degradosome, even though the degradosome contains active RhlB helicase which normally facilitates degradation of structured RNA. The exoribonucleolytic activity of the degradosome was due to polynucleotide phosphorylase, rather than the recently reported exonucleolytic activity exhibited by a purified fragment of RNase E (Huang, H., Liao, J., and Cohen, S. N. (1998) Nature 391, 99-102). Addition of a 3'-poly(A) tail stimulated degradation by the degradosome. As few as 5 adenosine residues were sufficient to achieve this stimulation, and generic sequences were equally effective. The data show that the degradosome requires a single-stranded "toehold" 3' to a secondary structure to recognize and degrade the RNA molecule efficiently; polyadenylation can provide this single-stranded 3'-end. Significantly, oligo(G) and oligo(U) tails were unable to stimulate degradation; for oligo(G), at least, this is probably due to the formation of a G quartet structure which makes the 3'-end inaccessible. The inaccessibility of 3'-oligo(U) sequences is likely to have a role in stabilization of RNA molecules generated by Rho-independent terminators.

MeSH Terms
ATP-Binding Cassette Transporters Bacterial Proteins/genetics Base Sequence Carrier Proteins/genetics Endoribonucleases/metabolism Escherichia coli Escherichia coli Proteins Maltose/genetics Maltose-Binding Proteins Molecular Sequence Data Monosaccharide Transport Proteins Multienzyme Complexes/metabolism Nucleic Acid Conformation Poly A/metabolism Polyribonucleotide Nucleotidyltransferase/metabolism RNA Helicases/metabolism RNA, Bacterial/metabolism RNA, Messenger/metabolism
Chemicals
ATP-Binding Cassette Transporters Bacterial Proteins Carrier Proteins Escherichia coli Proteins Maltose-Binding Proteins Monosaccharide Transport Proteins Multienzyme Complexes RNA, Bacterial RNA, Messenger degradosome maltose transport system, E coli Poly A Maltose Polyribonucleotide Nucleotidyltransferase Endoribonucleases RNA Helicases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Blum E
Nuffield Department of Clinical Biochemistry, Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, United Kingdom.
Carpousis A J
Higgins C F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1999-02-12
Pages
4009-16
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com