Literature DB >> 12270836

Pseudoknot-dependent translational coupling in repBA genes of the IncB plasmid pMU720 involves reinitiation.

J Praszkier1, A J Pittard.   

Abstract

Replication of the IncB miniplasmid pMU720 requires synthesis of the replication initiator protein, RepA, whose translation is coupled to that of a leader peptide, RepB. The unusual feature of this system is that translational coupling in repBA has to be activated by the formation of a pseudoknot immediately upstream of the repA Shine-Dalgarno sequence. A small antisense RNA, RNAI, controls replication of pMU720 by interacting with repBA mRNA to inhibit expression of repA both directly, by preventing formation of the pseudoknot, and indirectly, by inhibiting translation of repB. The mechanism of translational coupling in repBA was investigated using the specialized ribosome system, which directs a subpopulation of ribosomes that carry an altered anti-Shine-Dalgarno sequence to translate mRNA molecules whose Shine-Dalgarno sequences have been altered to be complementary to the mutant anti-Shine-Dalgarno sequence. Our data indicate that translation of repA involves reinitiation by the ribosome that has terminated translation of repB. The role of the pseudoknot in this process and its effect on the control of copy number in pMU720 are discussed.

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Year:  2002        PMID: 12270836      PMCID: PMC139621          DOI: 10.1128/JB.184.20.5772-5780.2002

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  35 in total

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Journal:  Biochim Biophys Acta       Date:  1951-11

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3.  Structural analysis of late intermediate complex formed between plasmid ColIb-P9 Inc RNA and its target RNA. How does a single antisense RNA repress translation of two genes at different rates?

Authors:  K Asano; K Mizobuchi
Journal:  J Biol Chem       Date:  2000-01-14       Impact factor: 5.157

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Authors:  B Berkhout; R A Kastelein; J van Duin
Journal:  Gene       Date:  1985       Impact factor: 3.688

5.  A ribosome binding site sequence is necessary for efficient expression of the distal gene of a translationally-coupled gene pair.

Authors:  A Das; C Yanofsky
Journal:  Nucleic Acids Res       Date:  1984-06-11       Impact factor: 16.971

6.  New versatile cloning and sequencing vectors based on bacteriophage M13.

Authors:  M P Kieny; R Lathe; J P Lecocq
Journal:  Gene       Date:  1983-12       Impact factor: 3.688

7.  New M13 vectors for cloning.

Authors:  J Messing
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

8.  Demonstration of a third incompatibility function on plasmids already incompatible with group P and group I plasmids.

Authors:  P I Bird; J Pittard
Journal:  Plasmid       Date:  1983-03       Impact factor: 3.466

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Journal:  Gene       Date:  1984-05       Impact factor: 3.688

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  4 in total

1.  A ProQ/FinO family protein involved in plasmid copy number control favours fitness of bacteria carrying mcr-1-bearing IncI2 plasmids.

Authors:  Jun Yang; Hai-Hong Wang; Yaoyao Lu; Ling-Xian Yi; Yinyue Deng; Luchao Lv; Vincent Burrus; Jian-Hua Liu
Journal:  Nucleic Acids Res       Date:  2021-04-19       Impact factor: 16.971

2.  The highly efficient translation initiation region from the Escherichia coli rpsA gene lacks a shine-dalgarno element.

Authors:  Patricia Skorski; Prune Leroy; Olivier Fayet; Marc Dreyfus; Sylvie Hermann-Le Denmat
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

Review 3.  Exposing plasmids as the Achilles' heel of drug-resistant bacteria.

Authors:  Julia J Williams; Paul J Hergenrother
Journal:  Curr Opin Chem Biol       Date:  2008-07-14       Impact factor: 8.822

Review 4.  Why is start codon selection so precise in eukaryotes?

Authors:  Katsura Asano
Journal:  Translation (Austin)       Date:  2014-03-12
  4 in total

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