Home LiteratureArticle Details
PMID: 1569014 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

The polycistronic mRNA of the Zymomonas mobilis glf-zwf-edd-glk operon is subject to complex transcript processing.

Journal of bacteriology ·Vol. 174 ·No. 9 ·1992-05-00 ·Pages 2824-33

Liu J, Barnell WO, Conway T

Abstract

The full-length 6.14-kb polycistronic glf-zwf-edd-glk mRNA from Zymomonas mobilis appears to be processed by endonucleolytic cleavage, resulting in the formation of several discrete transcripts. Northern analysis and transcript mapping revealed that the processed transcripts correspond to functional mono-, di-, or tricistronic messages. The relative abundance of the gene-specific, functional messages was measured. Expression of zwf and edd correlated well with functional message levels. Disproportionally high levels of the glk-specific mRNAs might compensate for the instability of glucokinase by allowing increased translation. The relative abundance of the discrete transcripts was shown to be a function of their respective decay rates. Northern analysis of the fate of the 6.14-kb transcript after inhibition of transcription by rifampin showed that the abundance of shorter, more stable transcripts increased at the expense of longer, less stable transcripts. This is suggestive of endonucleolytic mRNA processing. The most abundant 5' and 3' transcript ends were found to lie within secondary structures that probably impart stability to the most abundant mRNAs.

Related Genes
MeSH Terms
Base Sequence Chromosome Mapping Gram-Negative Facultatively Anaerobic Rods/genetics Molecular Sequence Data Nucleic Acid Conformation Operon/genetics RNA Precursors/metabolism RNA Processing, Post-Transcriptional RNA, Messenger/metabolism
Chemicals
RNA Precursors RNA, Messenger
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Liu J
School of Biological Sciences, University of Nebraska, Lincoln 68588-0118.
Barnell W O
Conway T
References (20)
20 references, click to expand
  1. Specific endonucleolytic cleavage of the mRNA for ribosomal protein S20 of Escherichia coli requires the product of the ams gene in vivo and in vitro.
    J Bacteriol. 1991 Apr;173(8):2488-97 PMID: 2013571
  2. A comprehensive set of sequence analysis programs for the VAX.
    Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387-95 PMID: 6546423
  3. Similarity of Escherichia coli propanediol oxidoreductase (fucO product) and an unusual alcohol dehydrogenase from Zymomonas mobilis and Saccharomyces cerevisiae.
    J Bacteriol. 1989 Jul;171(7):3754-9 PMID: 2661535
  4. Stabilization of the 3' one-third of Escherichia coli ribosomal protein S20 mRNA in mutants lacking polynucleotide phosphorylase.
    J Bacteriol. 1989 Aug;171(8):4112-20 PMID: 2666387
  5. Evidence for endonucleolytic cleavages in decay of lacZ and lacI mRNAs.
    J Bacteriol. 1988 Jun;170(6):2860-5 PMID: 2836375
  6. Simultaneous purification and characterization of glucokinase, fructokinase and glucose-6-phosphate dehydrogenase from Zymomonas mobilis.
    Biochem J. 1985 Jun 15;228(3):627-34 PMID: 2992451
  7. Site-specific endonucleolytic cleavages and the regulation of stability of E. coli ompA mRNA.
    Cell. 1988 Mar 25;52(6):893-901 PMID: 3280138
  8. Glycolytic flux in Zymomonas mobilis: enzyme and metabolite levels during batch fermentation.
    J Bacteriol. 1987 Aug;169(8):3726-36 PMID: 3611027
  9. The control of flux.
    Symp Soc Exp Biol. 1973;27:65-104 PMID: 4148886
  10. Use of differential dye-ligand chromatography with affinity elution for enzyme purification: 6-phosphogluconate dehydratase from Zymomonas mobilis.
    Anal Biochem. 1984 Feb;136(2):530-4 PMID: 6326623
  11. DNA sequencing with chain-terminating inhibitors.
    Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PMID: 271968
  12. The Zymomonas mobilis glf, zwf, edd, and glk genes form an operon: localization of the promoter and identification of a conserved sequence in the regulatory region.
    J Bacteriol. 1992 May;174(9):2816-23 PMID: 1569013
  13. Segmental message stabilization as a mechanism for differential expression from the Zymomonas mobilis gap operon.
    J Bacteriol. 1991 Jan;173(1):245-54 PMID: 1702780
  14. Cloning, characterization, and nucleotide sequence analysis of a Zymomonas mobilis phosphoglucose isomerase gene that is subject to carbon source-dependent regulation.
    J Bacteriol. 1991 May;173(10):3215-23 PMID: 1708765
  15. Intermediates in the degradation of mRNA from the lactose operon of Escherichia coli.
    Nucleic Acids Res. 1991 May 25;19(10):2767-76 PMID: 1710346
  16. Structure and function of a bacterial mRNA stabilizer: analysis of the 5' untranslated region of ompA mRNA.
    J Bacteriol. 1991 Aug;173(15):4578-86 PMID: 1713205
  17. Cloning, characterization and expression of the Zymononas mobilis eda gene that encodes 2-keto-3-deoxy-6-phosphogluconate aldolase of the Entner-Doudoroff pathway.
    Mol Microbiol. 1991 Dec;5(12):2901-11 PMID: 1809834
  18. RNase I*, a form of RNase I, and mRNA degradation in Escherichia coli.
    J Bacteriol. 1991 Aug;173(15):4653-9 PMID: 1856166
  19. Gel electrophoretic analysis of Zymomonas mobilis glycolytic and fermentative enzymes: identification of alcohol dehydrogenase II as a stress protein.
    J Bacteriol. 1991 Oct;173(19):5975-82 PMID: 1917831
  20. Sequence and genetic organization of a Zymomonas mobilis gene cluster that encodes several enzymes of glucose metabolism.
    J Bacteriol. 1990 Dec;172(12):7227-40 PMID: 2254282
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1992-05-00
Pages
2824-33
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC205933
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