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5′ isomiR variation is of functional and evolutionary importance

We have sequenced miRNA libraries from human embryonic, neural and foetal mesenchymal stem cells. We report that the majority of miRNA genes encode mature isomers that vary in size by one or more bases at the 3′ and/or 5′ end of the miRNA. Northern blotting for individual miRNAs showed that the prop...

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Autores principales: Tan, Geok Chin, Chan, Elcie, Molnar, Attila, Sarkar, Rupa, Alexieva, Diana, Isa, Ihsan Mad, Robinson, Sophie, Zhang, Shuchen, Ellis, Peter, Langford, Cordelia F., Guillot, Pascale V., Chandrashekran, Anil, Fisk, Nick M., Castellano, Leandro, Meister, Gunter, Winston, Robert M., Cui, Wei, Baulcombe, David, Dibb, Nick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132760/
https://www.ncbi.nlm.nih.gov/pubmed/25056318
http://dx.doi.org/10.1093/nar/gku656
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author Tan, Geok Chin
Chan, Elcie
Molnar, Attila
Sarkar, Rupa
Alexieva, Diana
Isa, Ihsan Mad
Robinson, Sophie
Zhang, Shuchen
Ellis, Peter
Langford, Cordelia F.
Guillot, Pascale V.
Chandrashekran, Anil
Fisk, Nick M.
Castellano, Leandro
Meister, Gunter
Winston, Robert M.
Cui, Wei
Baulcombe, David
Dibb, Nick J.
author_facet Tan, Geok Chin
Chan, Elcie
Molnar, Attila
Sarkar, Rupa
Alexieva, Diana
Isa, Ihsan Mad
Robinson, Sophie
Zhang, Shuchen
Ellis, Peter
Langford, Cordelia F.
Guillot, Pascale V.
Chandrashekran, Anil
Fisk, Nick M.
Castellano, Leandro
Meister, Gunter
Winston, Robert M.
Cui, Wei
Baulcombe, David
Dibb, Nick J.
author_sort Tan, Geok Chin
collection PubMed
description We have sequenced miRNA libraries from human embryonic, neural and foetal mesenchymal stem cells. We report that the majority of miRNA genes encode mature isomers that vary in size by one or more bases at the 3′ and/or 5′ end of the miRNA. Northern blotting for individual miRNAs showed that the proportions of isomiRs expressed by a single miRNA gene often differ between cell and tissue types. IsomiRs were readily co-immunoprecipitated with Argonaute proteins in vivo and were active in luciferase assays, indicating that they are functional. Bioinformatics analysis predicts substantial differences in targeting between miRNAs with minor 5′ differences and in support of this we report that a 5′ isomiR-9–1 gained the ability to inhibit the expression of DNMT3B and NCAM2 but lost the ability to inhibit CDH1 in vitro. This result was confirmed by the use of isomiR-specific sponges. Our analysis of the miRGator database indicates that a small percentage of human miRNA genes express isomiRs as the dominant transcript in certain cell types and analysis of miRBase shows that 5′ isomiRs have replaced canonical miRNAs many times during evolution. This strongly indicates that isomiRs are of functional importance and have contributed to the evolution of miRNA genes.
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spelling pubmed-41327602014-12-01 5′ isomiR variation is of functional and evolutionary importance Tan, Geok Chin Chan, Elcie Molnar, Attila Sarkar, Rupa Alexieva, Diana Isa, Ihsan Mad Robinson, Sophie Zhang, Shuchen Ellis, Peter Langford, Cordelia F. Guillot, Pascale V. Chandrashekran, Anil Fisk, Nick M. Castellano, Leandro Meister, Gunter Winston, Robert M. Cui, Wei Baulcombe, David Dibb, Nick J. Nucleic Acids Res RNA We have sequenced miRNA libraries from human embryonic, neural and foetal mesenchymal stem cells. We report that the majority of miRNA genes encode mature isomers that vary in size by one or more bases at the 3′ and/or 5′ end of the miRNA. Northern blotting for individual miRNAs showed that the proportions of isomiRs expressed by a single miRNA gene often differ between cell and tissue types. IsomiRs were readily co-immunoprecipitated with Argonaute proteins in vivo and were active in luciferase assays, indicating that they are functional. Bioinformatics analysis predicts substantial differences in targeting between miRNAs with minor 5′ differences and in support of this we report that a 5′ isomiR-9–1 gained the ability to inhibit the expression of DNMT3B and NCAM2 but lost the ability to inhibit CDH1 in vitro. This result was confirmed by the use of isomiR-specific sponges. Our analysis of the miRGator database indicates that a small percentage of human miRNA genes express isomiRs as the dominant transcript in certain cell types and analysis of miRBase shows that 5′ isomiRs have replaced canonical miRNAs many times during evolution. This strongly indicates that isomiRs are of functional importance and have contributed to the evolution of miRNA genes. Oxford University Press 2014-08-18 2014-07-23 /pmc/articles/PMC4132760/ /pubmed/25056318 http://dx.doi.org/10.1093/nar/gku656 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Tan, Geok Chin
Chan, Elcie
Molnar, Attila
Sarkar, Rupa
Alexieva, Diana
Isa, Ihsan Mad
Robinson, Sophie
Zhang, Shuchen
Ellis, Peter
Langford, Cordelia F.
Guillot, Pascale V.
Chandrashekran, Anil
Fisk, Nick M.
Castellano, Leandro
Meister, Gunter
Winston, Robert M.
Cui, Wei
Baulcombe, David
Dibb, Nick J.
5′ isomiR variation is of functional and evolutionary importance
title 5′ isomiR variation is of functional and evolutionary importance
title_full 5′ isomiR variation is of functional and evolutionary importance
title_fullStr 5′ isomiR variation is of functional and evolutionary importance
title_full_unstemmed 5′ isomiR variation is of functional and evolutionary importance
title_short 5′ isomiR variation is of functional and evolutionary importance
title_sort 5′ isomir variation is of functional and evolutionary importance
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132760/
https://www.ncbi.nlm.nih.gov/pubmed/25056318
http://dx.doi.org/10.1093/nar/gku656
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