Directional transition from initiation to elongation in bacterial translation
Descripción del Articulo
The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techn...
Autores: | , , , , |
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Formato: | artículo |
Fecha de Publicación: | 2015 |
Institución: | Universidad Peruana de Ciencias Aplicadas |
Repositorio: | UPC-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/579679 |
Enlace del recurso: | http://hdl.handle.net/10757/579679 |
Nivel de acceso: | acceso abierto |
Materia: | Elongation Bacterial translation Directional transition |
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dc.title.es_PE.fl_str_mv |
Directional transition from initiation to elongation in bacterial translation |
title |
Directional transition from initiation to elongation in bacterial translation |
spellingShingle |
Directional transition from initiation to elongation in bacterial translation Goyal, Akanksha Elongation Bacterial translation Directional transition |
title_short |
Directional transition from initiation to elongation in bacterial translation |
title_full |
Directional transition from initiation to elongation in bacterial translation |
title_fullStr |
Directional transition from initiation to elongation in bacterial translation |
title_full_unstemmed |
Directional transition from initiation to elongation in bacterial translation |
title_sort |
Directional transition from initiation to elongation in bacterial translation |
author |
Goyal, Akanksha |
author_facet |
Goyal, Akanksha Belardinelli, Riccardo Maracci, Cristina Milon, Pohl Rodnina, Marina V. |
author_role |
author |
author2 |
Belardinelli, Riccardo Maracci, Cristina Milon, Pohl Rodnina, Marina V. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Goyal, Akanksha Belardinelli, Riccardo Maracci, Cristina Milon, Pohl Rodnina, Marina V. |
dc.subject.es_PE.fl_str_mv |
Elongation Bacterial translation Directional transition |
topic |
Elongation Bacterial translation Directional transition |
description |
The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation. |
publishDate |
2015 |
dc.date.accessioned.es_PE.fl_str_mv |
2015-10-14T18:01:25Z |
dc.date.available.es_PE.fl_str_mv |
2015-10-14T18:01:25Z |
dc.date.issued.fl_str_mv |
2015-10-14 |
dc.type.es_PE.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
dc.identifier.issn.es_PE.fl_str_mv |
0305-1048 |
dc.identifier.doi.es_PE.fl_str_mv |
10.1093/nar/gkv869 |
dc.identifier.uri.es_PE.fl_str_mv |
http://hdl.handle.net/10757/579679 |
dc.identifier.eissn.es_PE.fl_str_mv |
1362-4962 |
dc.identifier.journal.es_PE.fl_str_mv |
Nucleic Acids Research (Nucleic Acids Research) |
identifier_str_mv |
0305-1048 10.1093/nar/gkv869 1362-4962 Nucleic Acids Research (Nucleic Acids Research) |
url |
http://hdl.handle.net/10757/579679 |
dc.language.iso.es_PE.fl_str_mv |
eng |
language |
eng |
dc.relation.url.es_PE.fl_str_mv |
http://nar.oxfordjournals.org/content/early/2015/09/03/nar.gkv869.full.pdf+html |
dc.rights.es_PE.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.es_PE.fl_str_mv |
application/pdf |
dc.publisher.es_PE.fl_str_mv |
Oxford University Press |
dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Académico - UPC |
dc.source.none.fl_str_mv |
reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
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Universidad Peruana de Ciencias Aplicadas |
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UPC |
institution |
UPC |
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UPC-Institucional |
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UPC-Institucional |
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Goyal, AkankshaBelardinelli, RiccardoMaracci, CristinaMilon, PohlRodnina, Marina V.2015-10-14T18:01:25Z2015-10-14T18:01:25Z2015-10-140305-104810.1093/nar/gkv869http://hdl.handle.net/10757/5796791362-4962Nucleic Acids Research (Nucleic Acids Research)The transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation.Boehringen Ingelheim Fonds and the G¨ottingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences (to A.G.); Max Planck Society and grants of the Deutsche Forschungsgemeinschaft (to M.V.R.); Peruvian Programa Nacional de Innovaci ´on para la Competitividad y Productividad [382-PNICP-PIBA-2014 (to P.M.)]. Funding for open access charge: Max Planck Society.Revisión por paresapplication/pdfengOxford University Presshttp://nar.oxfordjournals.org/content/early/2015/09/03/nar.gkv869.full.pdf+htmlinfo:eu-repo/semantics/openAccessUniversidad Peruana de Ciencias Aplicadas (UPC)Repositorio Académico - UPCreponame:UPC-Institucionalinstname:Universidad Peruana de Ciencias Aplicadasinstacron:UPCElongationBacterial translationDirectional transitionDirectional transition from initiation to elongation in bacterial translationinfo:eu-repo/semantics/article2018-06-22T21:41:06ZThe transition of the 30S initiation complex (IC) to the translating 70S ribosome after 50S subunit joining provides an important checkpoint for mRNA selection during translation in bacteria. Here, we study the timing and control of reactions that occur during 70S IC formation by rapid kinetic techniques, using a toolbox of fluorescence-labeled translation components. We present a kinetic model based on global fitting of time courses obtained with eight different reporters at increasing concentrations of 50S subunits. IF1 and IF3 together affect the kinetics of subunit joining, but do not alter the elemental rates of subsequent steps of 70S IC maturation. After 50S subunit joining, IF2-dependent reactions take place independent of the presence of IF1 or IF3. GTP hydrolysis triggers the efficient dissociation of fMet-tRNAfMet from IF2 and promotes the dissociation of IF2 and IF1 from the 70S IC, but does not affect IF3. The presence of non-hydrolyzable GTP analogs shifts the equilibrium towards a stable 70S–mRNA–IF1–IF2–fMet-tRNAfMet complex. Our kinetic analysis reveals the molecular choreography of the late stages in translation initiation.ORIGINALNucl. Acids Res.-2015-Goyal-nar-gkv869.pdfNucl. 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