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Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles
The functional unit of mobile group II introns is a ribonucleoprotein particle (RNP) consisting of the intron-encoded protein (IEP) and the excised intron RNA. The IEP has reverse transcriptase activity but also promotes RNA splicing, and the RNA-protein complex triggers site-specific DNA insertion...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037169/ https://www.ncbi.nlm.nih.gov/pubmed/27730127 http://dx.doi.org/10.3389/fmolb.2016.00058 |
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author | Molina-Sánchez, Maria D. García-Rodríguez, Fernando M. Toro, Nicolás |
author_facet | Molina-Sánchez, Maria D. García-Rodríguez, Fernando M. Toro, Nicolás |
author_sort | Molina-Sánchez, Maria D. |
collection | PubMed |
description | The functional unit of mobile group II introns is a ribonucleoprotein particle (RNP) consisting of the intron-encoded protein (IEP) and the excised intron RNA. The IEP has reverse transcriptase activity but also promotes RNA splicing, and the RNA-protein complex triggers site-specific DNA insertion by reverse splicing, in a process called retrohoming. In vitro reconstituted ribonucleoprotein complexes from the Lactococcus lactis group II intron Ll.LtrB, which produce a double strand break, have recently been studied as a means of developing group II intron-based gene targeting methods for higher organisms. The Sinorhizobium meliloti group II intron RmInt1 is an efficient mobile retroelement, the dispersal of which appears to be linked to transient single-stranded DNA during replication. The RmInt1IEP lacks the endonuclease domain (En) and cannot cut the bottom strand to generate the 3′ end to initiate reverse transcription. We used an Escherichia coli expression system to produce soluble and active RmInt1 IEP and reconstituted RNPs with purified components in vitro. The RNPs generated were functional and reverse-spliced into a single-stranded DNA target. This work constitutes the starting point for the use of group II introns lacking DNA endonuclease domain-derived RNPs for highly specific gene targeting methods. |
format | Online Article Text |
id | pubmed-5037169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50371692016-10-11 Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles Molina-Sánchez, Maria D. García-Rodríguez, Fernando M. Toro, Nicolás Front Mol Biosci Molecular Biosciences The functional unit of mobile group II introns is a ribonucleoprotein particle (RNP) consisting of the intron-encoded protein (IEP) and the excised intron RNA. The IEP has reverse transcriptase activity but also promotes RNA splicing, and the RNA-protein complex triggers site-specific DNA insertion by reverse splicing, in a process called retrohoming. In vitro reconstituted ribonucleoprotein complexes from the Lactococcus lactis group II intron Ll.LtrB, which produce a double strand break, have recently been studied as a means of developing group II intron-based gene targeting methods for higher organisms. The Sinorhizobium meliloti group II intron RmInt1 is an efficient mobile retroelement, the dispersal of which appears to be linked to transient single-stranded DNA during replication. The RmInt1IEP lacks the endonuclease domain (En) and cannot cut the bottom strand to generate the 3′ end to initiate reverse transcription. We used an Escherichia coli expression system to produce soluble and active RmInt1 IEP and reconstituted RNPs with purified components in vitro. The RNPs generated were functional and reverse-spliced into a single-stranded DNA target. This work constitutes the starting point for the use of group II introns lacking DNA endonuclease domain-derived RNPs for highly specific gene targeting methods. Frontiers Media S.A. 2016-09-27 /pmc/articles/PMC5037169/ /pubmed/27730127 http://dx.doi.org/10.3389/fmolb.2016.00058 Text en Copyright © 2016 Molina-Sánchez, García-Rodríguez and Toro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Molina-Sánchez, Maria D. García-Rodríguez, Fernando M. Toro, Nicolás Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title_full | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title_fullStr | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title_full_unstemmed | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title_short | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
title_sort | functionality of in vitro reconstituted group ii intron rmint1-derived ribonucleoprotein particles |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037169/ https://www.ncbi.nlm.nih.gov/pubmed/27730127 http://dx.doi.org/10.3389/fmolb.2016.00058 |
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