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Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224
Mirtrons are a recently described category of microRNA (miRNA) relying on splicing rather than processing by the microprocessor complex to generate pre-miRNA precursors of the RNA interference (RNAi) pathway. Their discovery and subsequent verification provides important information about a distinct...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479180/ https://www.ncbi.nlm.nih.gov/pubmed/22848108 http://dx.doi.org/10.1093/nar/gks712 |
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author | Sibley, Christopher R. Seow, Yiqi Curtis, Helen Weinberg, Marc S. Wood, Matthew J. A. |
author_facet | Sibley, Christopher R. Seow, Yiqi Curtis, Helen Weinberg, Marc S. Wood, Matthew J. A. |
author_sort | Sibley, Christopher R. |
collection | PubMed |
description | Mirtrons are a recently described category of microRNA (miRNA) relying on splicing rather than processing by the microprocessor complex to generate pre-miRNA precursors of the RNA interference (RNAi) pathway. Their discovery and subsequent verification provides important information about a distinct class of miRNA and inherent advantages that could be exploited to silence genes of interest. These include micro-processor-independent biogenesis, pol-II-dependent transcription, accurate species generation and the delivery of multiple artificial mirtrons as introns within a single host transcript. Here we determined the sequence motifs required for correct processing of the mmu-miR-1224 mirtron and incorporated these into artificial mirtrons targeting Parkinson’s disease-associated LRRK2 and α-synuclein genes. By incorporating these rules associated with processing and splicing, artificial mirtrons could be designed and made to silence complementary targets either at the mRNA or protein level. We further demonstrate with a LRRK2 targeting artificial mirtron that neuronal-specific silencing can be directed under the control of the human synapsin promoter. Finally, multiple mirtrons were co-delivered within a single host transcript, an eGFP reporter, to allow simultaneous targeting of two or more targets in a combinatorial approach. Thus, the unique characteristics of artificial mirtrons make this an attractive approach for future RNAi applications. |
format | Online Article Text |
id | pubmed-3479180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34791802012-10-24 Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 Sibley, Christopher R. Seow, Yiqi Curtis, Helen Weinberg, Marc S. Wood, Matthew J. A. Nucleic Acids Res RNA Mirtrons are a recently described category of microRNA (miRNA) relying on splicing rather than processing by the microprocessor complex to generate pre-miRNA precursors of the RNA interference (RNAi) pathway. Their discovery and subsequent verification provides important information about a distinct class of miRNA and inherent advantages that could be exploited to silence genes of interest. These include micro-processor-independent biogenesis, pol-II-dependent transcription, accurate species generation and the delivery of multiple artificial mirtrons as introns within a single host transcript. Here we determined the sequence motifs required for correct processing of the mmu-miR-1224 mirtron and incorporated these into artificial mirtrons targeting Parkinson’s disease-associated LRRK2 and α-synuclein genes. By incorporating these rules associated with processing and splicing, artificial mirtrons could be designed and made to silence complementary targets either at the mRNA or protein level. We further demonstrate with a LRRK2 targeting artificial mirtron that neuronal-specific silencing can be directed under the control of the human synapsin promoter. Finally, multiple mirtrons were co-delivered within a single host transcript, an eGFP reporter, to allow simultaneous targeting of two or more targets in a combinatorial approach. Thus, the unique characteristics of artificial mirtrons make this an attractive approach for future RNAi applications. Oxford University Press 2012-10 2012-07-30 /pmc/articles/PMC3479180/ /pubmed/22848108 http://dx.doi.org/10.1093/nar/gks712 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Sibley, Christopher R. Seow, Yiqi Curtis, Helen Weinberg, Marc S. Wood, Matthew J. A. Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title | Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title_full | Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title_fullStr | Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title_full_unstemmed | Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title_short | Silencing of Parkinson's disease-associated genes with artificial mirtron mimics of miR-1224 |
title_sort | silencing of parkinson's disease-associated genes with artificial mirtron mimics of mir-1224 |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479180/ https://www.ncbi.nlm.nih.gov/pubmed/22848108 http://dx.doi.org/10.1093/nar/gks712 |
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