PMID:2478715: Difference between revisions

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<span style = 'font-size: large'> '''Brown, S'''  (1989) Time of action of 4.5 S RNA in Escherichia coli translation.''J. Mol. Biol.'' '''209''':79-90</span>
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!align=left  |Citation
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'''Brown, S'''  (1989) Time of action of 4.5 S RNA in Escherichia coli translation. ''J. Mol. Biol.'' '''209''':79-90
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!align=left  |Abstract
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A new class of suppressor mutants helps to define the role of 4.5 S RNA in translation. The suppressors reduce the requirement for 4.5 S RNA by increasing the intracellular concentration of uncharged tRNA. Suppression probably occurs by prolonging the period in which translating ribosomes have translocated but not yet released the uncharged tRNA, indicating that this is the point at which 4.5 S RNA enters translation. The release of 4.5 S RNA from polysomes is affected by antibiotics that inhibit protein synthesis. The antibiotic-sensitivity of this release indicates that 4.5 S RNA exits the ribosome following translocation and prior to release of protein synthesis elongation factor G. These results indicate that 4.5 S RNA acts immediately after ribosomal translocation. A model is proposed in which 4.5 S RNA stabilizes the post-translocation state by replacing 23 S ribosomal RNA as a binding site for elongation factor G. The 4.5 S RNA-requirement of mutants altered in 23 S ribosomal RNA support this model.
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!align=left  |Links
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2478715 PubMed]


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|{{TableHeadingColor}} |'''Abstract''' || A new class of suppressor mutants helps to define the role of 4.5 S RNA in translation. The suppressors reduce the requirement for 4.5 S RNA by increasing the intracellular concentration of uncharged tRNA. Suppression probably occurs by prolonging the period in which translating ribosomes have translocated but not yet released the uncharged tRNA, indicating that this is the point at which 4.5 S RNA enters translation. The release of 4.5 S RNA from polysomes is affected by antibiotics that inhibit protein synthesis. The antibiotic-sensitivity of this release indicates that 4.5 S RNA exits the ribosome following translocation and prior to release of protein synthesis elongation factor G. These results indicate that 4.5 S RNA acts immediately after ribosomal translocation. A model is proposed in which 4.5 S RNA stabilizes the post-translocation state by replacing 23 S ribosomal RNA as a binding site for elongation factor G. The 4.5 S RNA-requirement of mutants altered in 23 S ribosomal RNA support this model.
!align=left  |Keywords
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Anti-Bacterial Agents/pharmacology; Escherichia coli/enzymology; Escherichia coli/genetics; Genes, Bacterial; Glutamate-tRNA Ligase/genetics; Mutation; Protein Biosynthesis; RNA, Bacterial/genetics; RNA, Ribosomal/genetics; RNA, Transfer/genetics; RNA, Transfer, Amino Acyl/genetics; Suppression, Genetic; Valine-tRNA Ligase/genetics
|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2478715 PubMed]
 
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!|Gene product!!Qualifier!!GO ID!!GO term name!!Evidence Code!!with/from!!Aspect!!Notes!!Status
 
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==EcoliWiki Links {{HelpIcon|Help:Literature}} ==
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Latest revision as of 04:44, 15 September 2013

Citation

Brown, S (1989) Time of action of 4.5 S RNA in Escherichia coli translation. J. Mol. Biol. 209:79-90

Abstract

A new class of suppressor mutants helps to define the role of 4.5 S RNA in translation. The suppressors reduce the requirement for 4.5 S RNA by increasing the intracellular concentration of uncharged tRNA. Suppression probably occurs by prolonging the period in which translating ribosomes have translocated but not yet released the uncharged tRNA, indicating that this is the point at which 4.5 S RNA enters translation. The release of 4.5 S RNA from polysomes is affected by antibiotics that inhibit protein synthesis. The antibiotic-sensitivity of this release indicates that 4.5 S RNA exits the ribosome following translocation and prior to release of protein synthesis elongation factor G. These results indicate that 4.5 S RNA acts immediately after ribosomal translocation. A model is proposed in which 4.5 S RNA stabilizes the post-translocation state by replacing 23 S ribosomal RNA as a binding site for elongation factor G. The 4.5 S RNA-requirement of mutants altered in 23 S ribosomal RNA support this model.

Links

PubMed

Keywords

Anti-Bacterial Agents/pharmacology; Escherichia coli/enzymology; Escherichia coli/genetics; Genes, Bacterial; Glutamate-tRNA Ligase/genetics; Mutation; Protein Biosynthesis; RNA, Bacterial/genetics; RNA, Ribosomal/genetics; RNA, Transfer/genetics; RNA, Transfer, Amino Acyl/genetics; Suppression, Genetic; Valine-tRNA Ligase/genetics

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