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Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata

Small non-coding RNAs such as miRNAs, piRNAs and endo-siRNAs fine-tune gene expression through post-transcriptional regulation, modulating important processes in development, differentiation, homeostasis and regeneration. Using deep sequencing, we have profiled small non-coding RNAs in Hydra magnipa...

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Autores principales: Krishna, Srikar, Nair, Aparna, Cheedipudi, Sirisha, Poduval, Deepak, Dhawan, Jyotsna, Palakodeti, Dasaradhi, Ghanekar, Yashoda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592418/
https://www.ncbi.nlm.nih.gov/pubmed/23166307
http://dx.doi.org/10.1093/nar/gks1020
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author Krishna, Srikar
Nair, Aparna
Cheedipudi, Sirisha
Poduval, Deepak
Dhawan, Jyotsna
Palakodeti, Dasaradhi
Ghanekar, Yashoda
author_facet Krishna, Srikar
Nair, Aparna
Cheedipudi, Sirisha
Poduval, Deepak
Dhawan, Jyotsna
Palakodeti, Dasaradhi
Ghanekar, Yashoda
author_sort Krishna, Srikar
collection PubMed
description Small non-coding RNAs such as miRNAs, piRNAs and endo-siRNAs fine-tune gene expression through post-transcriptional regulation, modulating important processes in development, differentiation, homeostasis and regeneration. Using deep sequencing, we have profiled small non-coding RNAs in Hydra magnipapillata and investigated changes in small RNA expression pattern during head regeneration. Our results reveal a unique repertoire of small RNAs in hydra. We have identified 126 miRNA loci; 123 of these miRNAs are unique to hydra. Less than 50% are conserved across two different strains of Hydra vulgaris tested in this study, indicating a highly diverse nature of hydra miRNAs in contrast to bilaterian miRNAs. We also identified siRNAs derived from precursors with perfect stem–loop structure and that arise from inverted repeats. piRNAs were the most abundant small RNAs in hydra, mapping to transposable elements, the annotated transcriptome and unique non-coding regions on the genome. piRNAs that map to transposable elements and the annotated transcriptome display a ping–pong signature. Further, we have identified several miRNAs and piRNAs whose expression is regulated during hydra head regeneration. Our study defines different classes of small RNAs in this cnidarian model system, which may play a role in orchestrating gene expression essential for hydra regeneration.
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spelling pubmed-35924182013-03-08 Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata Krishna, Srikar Nair, Aparna Cheedipudi, Sirisha Poduval, Deepak Dhawan, Jyotsna Palakodeti, Dasaradhi Ghanekar, Yashoda Nucleic Acids Res RNA Small non-coding RNAs such as miRNAs, piRNAs and endo-siRNAs fine-tune gene expression through post-transcriptional regulation, modulating important processes in development, differentiation, homeostasis and regeneration. Using deep sequencing, we have profiled small non-coding RNAs in Hydra magnipapillata and investigated changes in small RNA expression pattern during head regeneration. Our results reveal a unique repertoire of small RNAs in hydra. We have identified 126 miRNA loci; 123 of these miRNAs are unique to hydra. Less than 50% are conserved across two different strains of Hydra vulgaris tested in this study, indicating a highly diverse nature of hydra miRNAs in contrast to bilaterian miRNAs. We also identified siRNAs derived from precursors with perfect stem–loop structure and that arise from inverted repeats. piRNAs were the most abundant small RNAs in hydra, mapping to transposable elements, the annotated transcriptome and unique non-coding regions on the genome. piRNAs that map to transposable elements and the annotated transcriptome display a ping–pong signature. Further, we have identified several miRNAs and piRNAs whose expression is regulated during hydra head regeneration. Our study defines different classes of small RNAs in this cnidarian model system, which may play a role in orchestrating gene expression essential for hydra regeneration. Oxford University Press 2013-01 2012-11-19 /pmc/articles/PMC3592418/ /pubmed/23166307 http://dx.doi.org/10.1093/nar/gks1020 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 License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle RNA
Krishna, Srikar
Nair, Aparna
Cheedipudi, Sirisha
Poduval, Deepak
Dhawan, Jyotsna
Palakodeti, Dasaradhi
Ghanekar, Yashoda
Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title_full Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title_fullStr Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title_full_unstemmed Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title_short Deep sequencing reveals unique small RNA repertoire that is regulated during head regeneration in Hydra magnipapillata
title_sort deep sequencing reveals unique small rna repertoire that is regulated during head regeneration in hydra magnipapillata
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592418/
https://www.ncbi.nlm.nih.gov/pubmed/23166307
http://dx.doi.org/10.1093/nar/gks1020
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