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Characterization of piRNAs across postnatal development in mouse brain
PIWI-interacting RNAs (piRNAs) are responsible for maintaining the genome stability by silencing retrotransposons in germline tissues– where piRNAs were first discovered and thought to be restricted. Recently, novel functions were reported for piRNAs in germline and somatic cells. Using deep sequenc...
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/PMC4844963/ https://www.ncbi.nlm.nih.gov/pubmed/27112104 http://dx.doi.org/10.1038/srep25039 |
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author | Ghosheh, Yanal Seridi, Loqmane Ryu, Taewoo Takahashi, Hazuki Orlando, Valerio Carninci, Piero Ravasi, Timothy |
author_facet | Ghosheh, Yanal Seridi, Loqmane Ryu, Taewoo Takahashi, Hazuki Orlando, Valerio Carninci, Piero Ravasi, Timothy |
author_sort | Ghosheh, Yanal |
collection | PubMed |
description | PIWI-interacting RNAs (piRNAs) are responsible for maintaining the genome stability by silencing retrotransposons in germline tissues– where piRNAs were first discovered and thought to be restricted. Recently, novel functions were reported for piRNAs in germline and somatic cells. Using deep sequencing of small RNAs and CAGE of postnatal development of mouse brain, we identified piRNAs only in adult mouse brain. These piRNAs have similar sequence length as those of MILI-bound piRNAs. In addition, we predicted novel candidate regulators and putative targets of adult brain piRNAs. |
format | Online Article Text |
id | pubmed-4844963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48449632016-04-29 Characterization of piRNAs across postnatal development in mouse brain Ghosheh, Yanal Seridi, Loqmane Ryu, Taewoo Takahashi, Hazuki Orlando, Valerio Carninci, Piero Ravasi, Timothy Sci Rep Article PIWI-interacting RNAs (piRNAs) are responsible for maintaining the genome stability by silencing retrotransposons in germline tissues– where piRNAs were first discovered and thought to be restricted. Recently, novel functions were reported for piRNAs in germline and somatic cells. Using deep sequencing of small RNAs and CAGE of postnatal development of mouse brain, we identified piRNAs only in adult mouse brain. These piRNAs have similar sequence length as those of MILI-bound piRNAs. In addition, we predicted novel candidate regulators and putative targets of adult brain piRNAs. Nature Publishing Group 2016-04-26 /pmc/articles/PMC4844963/ /pubmed/27112104 http://dx.doi.org/10.1038/srep25039 Text en Copyright © 2016, Macmillan Publishers Limited 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 Ghosheh, Yanal Seridi, Loqmane Ryu, Taewoo Takahashi, Hazuki Orlando, Valerio Carninci, Piero Ravasi, Timothy Characterization of piRNAs across postnatal development in mouse brain |
title | Characterization of piRNAs across postnatal development in mouse brain |
title_full | Characterization of piRNAs across postnatal development in mouse brain |
title_fullStr | Characterization of piRNAs across postnatal development in mouse brain |
title_full_unstemmed | Characterization of piRNAs across postnatal development in mouse brain |
title_short | Characterization of piRNAs across postnatal development in mouse brain |
title_sort | characterization of pirnas across postnatal development in mouse brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844963/ https://www.ncbi.nlm.nih.gov/pubmed/27112104 http://dx.doi.org/10.1038/srep25039 |
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