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Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study
In the Avocado Sunblotch Viroid (ASBVd: 249-nt) from the Avsunviroidae family, a symmetric rolling-circle replication operates through an autocatalytic mechanism mediated by hammerhead ribozymes (HHR) embedded in both polarity strands. The concatenated multimeric ASBVd (+) and ASBVd (−) RNAs thus ge...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960562/ https://www.ncbi.nlm.nih.gov/pubmed/27456224 http://dx.doi.org/10.1038/srep30287 |
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author | Leclerc, Fabrice Zaccai, Giuseppe Vergne, Jacques Řìhovà, Martina Martel, Anne Maurel, Marie-Christine |
author_facet | Leclerc, Fabrice Zaccai, Giuseppe Vergne, Jacques Řìhovà, Martina Martel, Anne Maurel, Marie-Christine |
author_sort | Leclerc, Fabrice |
collection | PubMed |
description | In the Avocado Sunblotch Viroid (ASBVd: 249-nt) from the Avsunviroidae family, a symmetric rolling-circle replication operates through an autocatalytic mechanism mediated by hammerhead ribozymes (HHR) embedded in both polarity strands. The concatenated multimeric ASBVd (+) and ASBVd (−) RNAs thus generated are processed by cleavage to unit-length where ASBVd (−) self-cleaves with more efficiency. Absolute scale small angle neutron scattering (SANS) revealed a temperature-dependent dimer association in both ASBVd (−) and its derived 79-nt HHR (−). A joint thermodynamic analysis of SANS and catalytic data indicates the rate-determining step corresponds to the dimer/monomer transition. 2D and 3D models of monomeric and dimeric HHR (−) suggest that the inter-molecular contacts stabilizing the dimer (between HI and HII domains) compete with the intra-molecular ones stabilizing the active conformation of the full-length HHR required for an efficient self-cleavage. Similar competing intra- and inter-molecular contacts are proposed in ASBVd (−) though with a remoter region from an extension of the HI domain. |
format | Online Article Text |
id | pubmed-4960562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49605622016-08-05 Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study Leclerc, Fabrice Zaccai, Giuseppe Vergne, Jacques Řìhovà, Martina Martel, Anne Maurel, Marie-Christine Sci Rep Article In the Avocado Sunblotch Viroid (ASBVd: 249-nt) from the Avsunviroidae family, a symmetric rolling-circle replication operates through an autocatalytic mechanism mediated by hammerhead ribozymes (HHR) embedded in both polarity strands. The concatenated multimeric ASBVd (+) and ASBVd (−) RNAs thus generated are processed by cleavage to unit-length where ASBVd (−) self-cleaves with more efficiency. Absolute scale small angle neutron scattering (SANS) revealed a temperature-dependent dimer association in both ASBVd (−) and its derived 79-nt HHR (−). A joint thermodynamic analysis of SANS and catalytic data indicates the rate-determining step corresponds to the dimer/monomer transition. 2D and 3D models of monomeric and dimeric HHR (−) suggest that the inter-molecular contacts stabilizing the dimer (between HI and HII domains) compete with the intra-molecular ones stabilizing the active conformation of the full-length HHR required for an efficient self-cleavage. Similar competing intra- and inter-molecular contacts are proposed in ASBVd (−) though with a remoter region from an extension of the HI domain. Nature Publishing Group 2016-07-26 /pmc/articles/PMC4960562/ /pubmed/27456224 http://dx.doi.org/10.1038/srep30287 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Leclerc, Fabrice Zaccai, Giuseppe Vergne, Jacques Řìhovà, Martina Martel, Anne Maurel, Marie-Christine Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title | Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title_full | Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title_fullStr | Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title_full_unstemmed | Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title_short | Self-assembly Controls Self-cleavage of HHR from ASBVd (−): a Combined SANS and Modeling Study |
title_sort | self-assembly controls self-cleavage of hhr from asbvd (−): a combined sans and modeling study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960562/ https://www.ncbi.nlm.nih.gov/pubmed/27456224 http://dx.doi.org/10.1038/srep30287 |
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