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Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes
BACKGROUND: microRNAs (miRNAs) in fish have not been as extensively studied as those in mammals. The fish species Takifugu rubripes is an intensively studied model organism whose genome has been sequenced. The T. rubripes genome is approximately eight times smaller than the human genome, but has a s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469249/ https://www.ncbi.nlm.nih.gov/pubmed/26078057 http://dx.doi.org/10.1186/s12864-015-1622-1 |
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author | Wongwarangkana, Chaninya Fujimori, Kazuhiro E. Akiba, Masaki Kinoshita, Shigeharu Teruya, Morimi Nezuo, Maiko Masatoshi, Tsukahara Watabe, Shugo Asakawa, Shuichi |
author_facet | Wongwarangkana, Chaninya Fujimori, Kazuhiro E. Akiba, Masaki Kinoshita, Shigeharu Teruya, Morimi Nezuo, Maiko Masatoshi, Tsukahara Watabe, Shugo Asakawa, Shuichi |
author_sort | Wongwarangkana, Chaninya |
collection | PubMed |
description | BACKGROUND: microRNAs (miRNAs) in fish have not been as extensively studied as those in mammals. The fish species Takifugu rubripes is an intensively studied model organism whose genome has been sequenced. The T. rubripes genome is approximately eight times smaller than the human genome, but has a similar repertoire of protein-coding genes. Therefore, it is useful for identifying non-coding genes, including miRNA genes. To identify miRNA expression patterns in different organs of T. rubripes and give fundamental information to aid understanding of miRNA populations in this species, we extracted small RNAs from tissues and performed deep sequencing analysis to profile T. rubripes miRNAs. These data will be of assistance in functional studies of miRNAs in T. rubripes. RESULTS: After analyzing a total of 139 million reads, we found miRNA species in nine tissues (fast and slow muscles, heart, eye, brain, intestine, liver, ovaries, and testes). We identified 1420 known miRNAs, many of which were strongly expressed in certain tissues with expression patterns similar to those described for other animals in previous reports. Most miRNAs were expressed in tissues other than the ovaries or testes. However, some miRNA families were highly abundant in the gonads, but expressed only at low levels in somatic tissue, suggesting specific function in germ cells. The most abundant isomiRs (miRNA variants) of many miRNAs had identical sequences in the 5′ region. However, isomiRs of some miRNAs, including fru-miR-462-5p, varied in the 5′ region in some tissues, suggesting that they may target different mRNA transcripts. Longer small RNAs (26–31 nt), which were abundant in the gonads, may be putative piRNAs because of their length and their origin from repetitive elements. Additionally, our data include possible novel classes of small RNAs. CONCLUSIONS: We elucidated miRNA expression patterns in various organs of T. rubripes. Most miRNA sequences are conserved in vertebrates, indicating that the basic functions of vertebrate miRNAs share a common evolution. Some miRNA species exhibit different distributions of isomiRs between tissues, suggesting that they have a broad range of functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1622-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4469249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44692492015-06-17 Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes Wongwarangkana, Chaninya Fujimori, Kazuhiro E. Akiba, Masaki Kinoshita, Shigeharu Teruya, Morimi Nezuo, Maiko Masatoshi, Tsukahara Watabe, Shugo Asakawa, Shuichi BMC Genomics Research Article BACKGROUND: microRNAs (miRNAs) in fish have not been as extensively studied as those in mammals. The fish species Takifugu rubripes is an intensively studied model organism whose genome has been sequenced. The T. rubripes genome is approximately eight times smaller than the human genome, but has a similar repertoire of protein-coding genes. Therefore, it is useful for identifying non-coding genes, including miRNA genes. To identify miRNA expression patterns in different organs of T. rubripes and give fundamental information to aid understanding of miRNA populations in this species, we extracted small RNAs from tissues and performed deep sequencing analysis to profile T. rubripes miRNAs. These data will be of assistance in functional studies of miRNAs in T. rubripes. RESULTS: After analyzing a total of 139 million reads, we found miRNA species in nine tissues (fast and slow muscles, heart, eye, brain, intestine, liver, ovaries, and testes). We identified 1420 known miRNAs, many of which were strongly expressed in certain tissues with expression patterns similar to those described for other animals in previous reports. Most miRNAs were expressed in tissues other than the ovaries or testes. However, some miRNA families were highly abundant in the gonads, but expressed only at low levels in somatic tissue, suggesting specific function in germ cells. The most abundant isomiRs (miRNA variants) of many miRNAs had identical sequences in the 5′ region. However, isomiRs of some miRNAs, including fru-miR-462-5p, varied in the 5′ region in some tissues, suggesting that they may target different mRNA transcripts. Longer small RNAs (26–31 nt), which were abundant in the gonads, may be putative piRNAs because of their length and their origin from repetitive elements. Additionally, our data include possible novel classes of small RNAs. CONCLUSIONS: We elucidated miRNA expression patterns in various organs of T. rubripes. Most miRNA sequences are conserved in vertebrates, indicating that the basic functions of vertebrate miRNAs share a common evolution. Some miRNA species exhibit different distributions of isomiRs between tissues, suggesting that they have a broad range of functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1622-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-16 /pmc/articles/PMC4469249/ /pubmed/26078057 http://dx.doi.org/10.1186/s12864-015-1622-1 Text en © Wongwarangkana et al. 2015 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wongwarangkana, Chaninya Fujimori, Kazuhiro E. Akiba, Masaki Kinoshita, Shigeharu Teruya, Morimi Nezuo, Maiko Masatoshi, Tsukahara Watabe, Shugo Asakawa, Shuichi Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title | Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title_full | Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title_fullStr | Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title_full_unstemmed | Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title_short | Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes |
title_sort | deep sequencing, profiling and detailed annotation of micrornas in takifugu rubripes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469249/ https://www.ncbi.nlm.nih.gov/pubmed/26078057 http://dx.doi.org/10.1186/s12864-015-1622-1 |
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