Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome
- Autores
- Alvarez, Diego Ezequiel; Lodeiro, María F.; Ludueña, Silvio Juan; Pietrasanta, Lia; Gamarnik, Andrea Vanesa
- Año de publicación
- 2005
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Secondary and tertiary RNA structures present in viral RNA genomes play essential regulatory roles during translation, RNA replication, and assembly of new viral particles. In the case of flaviviruses, RNA-RNA interactions between the 5′ and 3′ ends of the genome have been proposed to be required for RNA replication. We found that two RNA elements present at the ends of the dengue virus genome interact in vitro with high affinity. Visualization of individual molecules by atomic force microscopy reveled that physical interaction between these RNA elements results in cyclization of the viral RNA. Using RNA binding assays, we found that the putative cyclization sequences, known as 5′ and 3′ CS, present in all mosquito-borne flaviviruses, were necessary but not sufficient for RNA-RNA interaction. Additional sequences present at the 5′ and 3′ untranslated regions of the viral RNA were also required for RNA-RNA complex formation. We named these sequences 5′ and 3′ UAR (upstream AUG region). In order to investigate the functional role of 5′-3′ UAR complementarity, these sequences were mutated either separately, to destroy base pairing, or simultaneously, to restore complementarity in the context of full-length dengue virus RNA. Nonviable viruses were recovered after transfection of dengue virus RNA carrying mutations either at the 5′ or 3′ UAR, while the RNA containing the compensatory mutations was able to replicate. Since sequence complementarity between the ends of the genome is required for dengue virus viability, we propose that cyclization of the RNA is a required conformation for viral replication.
Fil: Alvarez, Diego Ezequiel. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Lodeiro, María F.. Fundación Instituto Leloir; Argentina
Fil: Ludueña, Silvio Juan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Pietrasanta, Lia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fundación Instituto Leloir; Argentina - Materia
-
Flavivirus
Rna-Rna Interactions
Cyclization
Afm
Dengue Virus - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/41649
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/41649 |
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network_name_str |
CONICET Digital (CONICET) |
spelling |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus GenomeAlvarez, Diego EzequielLodeiro, María F.Ludueña, Silvio JuanPietrasanta, LiaGamarnik, Andrea VanesaFlavivirusRna-Rna InteractionsCyclizationAfmDengue Virushttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Secondary and tertiary RNA structures present in viral RNA genomes play essential regulatory roles during translation, RNA replication, and assembly of new viral particles. In the case of flaviviruses, RNA-RNA interactions between the 5′ and 3′ ends of the genome have been proposed to be required for RNA replication. We found that two RNA elements present at the ends of the dengue virus genome interact in vitro with high affinity. Visualization of individual molecules by atomic force microscopy reveled that physical interaction between these RNA elements results in cyclization of the viral RNA. Using RNA binding assays, we found that the putative cyclization sequences, known as 5′ and 3′ CS, present in all mosquito-borne flaviviruses, were necessary but not sufficient for RNA-RNA interaction. Additional sequences present at the 5′ and 3′ untranslated regions of the viral RNA were also required for RNA-RNA complex formation. We named these sequences 5′ and 3′ UAR (upstream AUG region). In order to investigate the functional role of 5′-3′ UAR complementarity, these sequences were mutated either separately, to destroy base pairing, or simultaneously, to restore complementarity in the context of full-length dengue virus RNA. Nonviable viruses were recovered after transfection of dengue virus RNA carrying mutations either at the 5′ or 3′ UAR, while the RNA containing the compensatory mutations was able to replicate. Since sequence complementarity between the ends of the genome is required for dengue virus viability, we propose that cyclization of the RNA is a required conformation for viral replication.Fil: Alvarez, Diego Ezequiel. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Lodeiro, María F.. Fundación Instituto Leloir; ArgentinaFil: Ludueña, Silvio Juan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Pietrasanta, Lia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fundación Instituto Leloir; ArgentinaAmerican Society for Microbiology2005-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/41649Alvarez, Diego Ezequiel; Lodeiro, María F.; Ludueña, Silvio Juan; Pietrasanta, Lia; Gamarnik, Andrea Vanesa; Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome; American Society for Microbiology; Journal of Virology; 79; 11; 5-2005; 6631-66430022-538XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112138/info:eu-repo/semantics/altIdentifier/doi/10.1128%2FJVI.79.11.6631-6643.2005info:eu-repo/semantics/altIdentifier/url/http://jvi.asm.org/content/79/11/6631info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:02:17Zoai:ri.conicet.gov.ar:11336/41649instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:02:17.602CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
title |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
spellingShingle |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome Alvarez, Diego Ezequiel Flavivirus Rna-Rna Interactions Cyclization Afm Dengue Virus |
title_short |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
title_full |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
title_fullStr |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
title_full_unstemmed |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
title_sort |
Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome |
dc.creator.none.fl_str_mv |
Alvarez, Diego Ezequiel Lodeiro, María F. Ludueña, Silvio Juan Pietrasanta, Lia Gamarnik, Andrea Vanesa |
author |
Alvarez, Diego Ezequiel |
author_facet |
Alvarez, Diego Ezequiel Lodeiro, María F. Ludueña, Silvio Juan Pietrasanta, Lia Gamarnik, Andrea Vanesa |
author_role |
author |
author2 |
Lodeiro, María F. Ludueña, Silvio Juan Pietrasanta, Lia Gamarnik, Andrea Vanesa |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Flavivirus Rna-Rna Interactions Cyclization Afm Dengue Virus |
topic |
Flavivirus Rna-Rna Interactions Cyclization Afm Dengue Virus |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Secondary and tertiary RNA structures present in viral RNA genomes play essential regulatory roles during translation, RNA replication, and assembly of new viral particles. In the case of flaviviruses, RNA-RNA interactions between the 5′ and 3′ ends of the genome have been proposed to be required for RNA replication. We found that two RNA elements present at the ends of the dengue virus genome interact in vitro with high affinity. Visualization of individual molecules by atomic force microscopy reveled that physical interaction between these RNA elements results in cyclization of the viral RNA. Using RNA binding assays, we found that the putative cyclization sequences, known as 5′ and 3′ CS, present in all mosquito-borne flaviviruses, were necessary but not sufficient for RNA-RNA interaction. Additional sequences present at the 5′ and 3′ untranslated regions of the viral RNA were also required for RNA-RNA complex formation. We named these sequences 5′ and 3′ UAR (upstream AUG region). In order to investigate the functional role of 5′-3′ UAR complementarity, these sequences were mutated either separately, to destroy base pairing, or simultaneously, to restore complementarity in the context of full-length dengue virus RNA. Nonviable viruses were recovered after transfection of dengue virus RNA carrying mutations either at the 5′ or 3′ UAR, while the RNA containing the compensatory mutations was able to replicate. Since sequence complementarity between the ends of the genome is required for dengue virus viability, we propose that cyclization of the RNA is a required conformation for viral replication. Fil: Alvarez, Diego Ezequiel. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Lodeiro, María F.. Fundación Instituto Leloir; Argentina Fil: Ludueña, Silvio Juan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina Fil: Pietrasanta, Lia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina Fil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fundación Instituto Leloir; Argentina |
description |
Secondary and tertiary RNA structures present in viral RNA genomes play essential regulatory roles during translation, RNA replication, and assembly of new viral particles. In the case of flaviviruses, RNA-RNA interactions between the 5′ and 3′ ends of the genome have been proposed to be required for RNA replication. We found that two RNA elements present at the ends of the dengue virus genome interact in vitro with high affinity. Visualization of individual molecules by atomic force microscopy reveled that physical interaction between these RNA elements results in cyclization of the viral RNA. Using RNA binding assays, we found that the putative cyclization sequences, known as 5′ and 3′ CS, present in all mosquito-borne flaviviruses, were necessary but not sufficient for RNA-RNA interaction. Additional sequences present at the 5′ and 3′ untranslated regions of the viral RNA were also required for RNA-RNA complex formation. We named these sequences 5′ and 3′ UAR (upstream AUG region). In order to investigate the functional role of 5′-3′ UAR complementarity, these sequences were mutated either separately, to destroy base pairing, or simultaneously, to restore complementarity in the context of full-length dengue virus RNA. Nonviable viruses were recovered after transfection of dengue virus RNA carrying mutations either at the 5′ or 3′ UAR, while the RNA containing the compensatory mutations was able to replicate. Since sequence complementarity between the ends of the genome is required for dengue virus viability, we propose that cyclization of the RNA is a required conformation for viral replication. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/41649 Alvarez, Diego Ezequiel; Lodeiro, María F.; Ludueña, Silvio Juan; Pietrasanta, Lia; Gamarnik, Andrea Vanesa; Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome; American Society for Microbiology; Journal of Virology; 79; 11; 5-2005; 6631-6643 0022-538X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/41649 |
identifier_str_mv |
Alvarez, Diego Ezequiel; Lodeiro, María F.; Ludueña, Silvio Juan; Pietrasanta, Lia; Gamarnik, Andrea Vanesa; Long-Range RNA-RNA Interactions Circularize the Dengue Virus Genome; American Society for Microbiology; Journal of Virology; 79; 11; 5-2005; 6631-6643 0022-538X CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112138/ info:eu-repo/semantics/altIdentifier/doi/10.1128%2FJVI.79.11.6631-6643.2005 info:eu-repo/semantics/altIdentifier/url/http://jvi.asm.org/content/79/11/6631 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Society for Microbiology |
publisher.none.fl_str_mv |
American Society for Microbiology |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269749083373568 |
score |
13.13397 |