uu.seUppsala University Publications
Change search
ReferencesLink to record
Permanent link

Direct link
Structure, function and metabolic stability of antisense RNAs
Uppsala University, Department of Microbiology.
1997 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Antisense RNAs usually are small, highly structured, unstable RNAs that control a varietyof different biological processes. They exert their effect by binding to complementarytarget RNAs and thereby inhibit their functions.

This thesis is concerned with the main features that determine the efficiency of antisense RNAs: their metabolic stability, the binding rate between antisense and target RNA, and the structure of the antisense RNA itself. Three different plasmid-encoded antisense RNAs were studied.

RNA decay in bacteria is complex: a large number of proteins are involved in processing and degradation. My results show that mutations in an Escherichia coli gene, pcnB, encoding a poly(A)polymerase, exert an effect on the replication of antisense RNA-regulated plasmids. PcnB aids in the degradation of the inhibitors of replication, the antisense RNAs. This enzyme can polyadenylate both CopA and RNAI, the antisense RNAs controlling the replication of plasmids R1 and ColE1, respectively. Accelerated pcnB dependent decay of CopA requires processing by an endoribonuclease, RNase E. This cleavage step appears to initiate decay of both CopA and RNA I. In addition, the 3'-5' exoribonucleases PNPase and RNase II can independently degrade RNase E-cleaved CopA.Other ribonucleases are involved in the pcnB dependent degradation since CopA decay is shown (although at lower rates) in the absence of these enzymes.

Analysis of FinP, an antisense RNA controlling plasmid conjugation, indicates astructure consisting of two stem-loops. Stem-loops are preferred motifs in most antisenseRNAs. The binding rate between FinP and its target RNA is in the same range as in otherwell-characterized systems. Upon binding, the target RNA (traJ mRNA) is renderedunstable, probably due to RNase III-dependent cleavages. This destabilization requiresthe presence of the helper protein FinO.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis , 1997. , 60 p.
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1104-232X ; 253
Keyword [en]
Keyword [sv]
National Category
Research subject
URN: urn:nbn:se:uu:diva-828ISBN: 91-554-3898-9OAI: oai:DiVA.org:uu-828DiVA: diva2:170892
Public defence
1997-01-31, Lecture room B42, Biomedical Center (BMC), Uppsala, Uppsala, 13:00
Available from: 1997-01-10 Created: 1997-01-10Bibliographically approved

Open Access in DiVA

No full text
Buy this publication >>

By organisation
Department of Microbiology

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Total: 75 hits
ReferencesLink to record
Permanent link

Direct link