The 5' leader of the human immunodeficiency virus type 1 (HIV-1) genomic RNA harbors an internal ribosome entry site (IRES) that is functional during the G2/M phase of the cell cycle. Here we show that translation initiation mediated by the HIV-1 IRES requires the participation of trans-acting cellular factors other than the canonical translational machinery. We used 'standard' chemical and enzymatic probes and an 'RNA SHAPE' analysis to model the structure of the HIV-1 5' leader and we show, by means of a footprinting assay, that G2/M extracts provide protections to regions previously identified as crucial for HIV-1 IRES activity. We also assessed the impact of mutations on IRES function. Strikingly, mutations did not significantly affect IRES activity suggesting that the requirement for pre-formed stable secondary or tertiary structure within the HIV-1 IRES may not be as strict as has been described for other viral IRESes. Finally, we used a proteomic approach to identify cellular proteins within the G2/M extracts that interact with the HIV-1 5' leader. Together, data show that HIV-1 IRES-mediated translation initiation is modulated by cellular proteins.
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Autor | Vallejos, Maricarmen Deforges, Jules Plank, Terra Dawn M. Letelier, Alejandro Ramdohr, Pablo Abraham, Christopher G. Valiente Echeverria, Fernando Kieft, Jeffrey S. Sargueil, Bruno Lopez Lastra, Marcelo |
Título | Activity of the human immunodeficiency virus type 1 cell cycle-dependent internal ribosomal entry site is modulated by IRES trans-acting factors |
Revista | NUCLEIC ACIDS RESEARCH |
ISSN | 0305-1048 |
ISSN electrónico | 1362-4962 |
Volumen | 39 |
Número de publicación | 14 |
Página inicio | 6186 |
Página final | 6200 |
Fecha de publicación | 2011 |
Resumen | The 5' leader of the human immunodeficiency virus type 1 (HIV-1) genomic RNA harbors an internal ribosome entry site (IRES) that is functional during the G2/M phase of the cell cycle. Here we show that translation initiation mediated by the HIV-1 IRES requires the participation of trans-acting cellular factors other than the canonical translational machinery. We used 'standard' chemical and enzymatic probes and an 'RNA SHAPE' analysis to model the structure of the HIV-1 5' leader and we show, by means of a footprinting assay, that G2/M extracts provide protections to regions previously identified as crucial for HIV-1 IRES activity. We also assessed the impact of mutations on IRES function. Strikingly, mutations did not significantly affect IRES activity suggesting that the requirement for pre-formed stable secondary or tertiary structure within the HIV-1 IRES may not be as strict as has been described for other viral IRESes. Finally, we used a proteomic approach to identify cellular proteins within the G2/M extracts that interact with the HIV-1 5' leader. Together, data show that HIV-1 IRES-mediated translation initiation is modulated by cellular proteins. |
Derechos | acceso abierto |
Agencia financiadora | FONDECYT Proyecto Nucleo Milenio CNRS-CONICYT Escuela de Medicina de la Pontificia Universidad Catolica de Chile CONICYT Agence Nationale de Recherche contre le SIDA (ANRS) for B.S. Laboratory work 'ATIP' from CNRS SIDACTION National Institutes of Health le Ministere de l'Education et de la Recherche VRI-Pontificia Universidad Catolica de Chile Comision Nacional de Investigacion Cientifica y Tecnologica, Gobierno de Chile, CONICYT through grant FONDECYT CNRS-DRI NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES |
DOI | 10.1093/nar/gkr189 |
Editorial | OXFORD UNIV PRESS |
Enlace | |
Id de publicación en Pubmed | MEDLINE:21482538 |
Id de publicación en WoS | WOS:000293919600037 |
Paginación | 15 páginas |
Palabra clave | HIV-1 TAT PROTEIN RNA SECONDARY STRUCTURE MESSENGER-RNA IN-VITRO TRANSLATION INITIATION TOPOISOMERASE-I POLIOVIRUS RNA REGION CAP CLEAVAGE |
Tema ODS | 03 Good Health and Well-being |
Tema ODS español | 03 Salud y bienestar |
Tipo de documento | artículo |