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miRTarBase: a database curates experimentally validated microRNA–target interactions
MicroRNAs (miRNAs), i.e. small non-coding RNA molecules (∼22 nt), can bind to one or more target sites on a gene transcript to negatively regulate protein expression, subsequently controlling many cellular mechanisms. A current and curated collection of miRNA–target interactions (MTIs) with experime...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013699/ https://www.ncbi.nlm.nih.gov/pubmed/21071411 http://dx.doi.org/10.1093/nar/gkq1107 |
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author | Hsu, Sheng-Da Lin, Feng-Mao Wu, Wei-Yun Liang, Chao Huang, Wei-Chih Chan, Wen-Ling Tsai, Wen-Ting Chen, Goun-Zhou Lee, Chia-Jung Chiu, Chih-Min Chien, Chia-Hung Wu, Ming-Chia Huang, Chi-Ying Tsou, Ann-Ping Huang, Hsien-Da |
author_facet | Hsu, Sheng-Da Lin, Feng-Mao Wu, Wei-Yun Liang, Chao Huang, Wei-Chih Chan, Wen-Ling Tsai, Wen-Ting Chen, Goun-Zhou Lee, Chia-Jung Chiu, Chih-Min Chien, Chia-Hung Wu, Ming-Chia Huang, Chi-Ying Tsou, Ann-Ping Huang, Hsien-Da |
author_sort | Hsu, Sheng-Da |
collection | PubMed |
description | MicroRNAs (miRNAs), i.e. small non-coding RNA molecules (∼22 nt), can bind to one or more target sites on a gene transcript to negatively regulate protein expression, subsequently controlling many cellular mechanisms. A current and curated collection of miRNA–target interactions (MTIs) with experimental support is essential to thoroughly elucidating miRNA functions under different conditions and in different species. As a database, miRTarBase has accumulated more than 3500 MTIs by manually surveying pertinent literature after data mining of the text systematically to filter research articles related to functional studies of miRNAs. Generally, the collected MTIs are validated experimentally by reporter assays, western blot, or microarray experiments with overexpression or knockdown of miRNAs. miRTarBase curates 3576 experimentally verified MTIs between 657 miRNAs and 2297 target genes among 17 species. miRTarBase contains the largest amount of validated MTIs by comparing with other similar, previously developed databases. The MTIs collected in the miRTarBase can also provide a large amount of positive samples to develop computational methods capable of identifying miRNA–target interactions. miRTarBase is now available on http://miRTarBase.mbc.nctu.edu.tw/, and is updated frequently by continuously surveying research articles. |
format | Text |
id | pubmed-3013699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30136992011-01-03 miRTarBase: a database curates experimentally validated microRNA–target interactions Hsu, Sheng-Da Lin, Feng-Mao Wu, Wei-Yun Liang, Chao Huang, Wei-Chih Chan, Wen-Ling Tsai, Wen-Ting Chen, Goun-Zhou Lee, Chia-Jung Chiu, Chih-Min Chien, Chia-Hung Wu, Ming-Chia Huang, Chi-Ying Tsou, Ann-Ping Huang, Hsien-Da Nucleic Acids Res Articles MicroRNAs (miRNAs), i.e. small non-coding RNA molecules (∼22 nt), can bind to one or more target sites on a gene transcript to negatively regulate protein expression, subsequently controlling many cellular mechanisms. A current and curated collection of miRNA–target interactions (MTIs) with experimental support is essential to thoroughly elucidating miRNA functions under different conditions and in different species. As a database, miRTarBase has accumulated more than 3500 MTIs by manually surveying pertinent literature after data mining of the text systematically to filter research articles related to functional studies of miRNAs. Generally, the collected MTIs are validated experimentally by reporter assays, western blot, or microarray experiments with overexpression or knockdown of miRNAs. miRTarBase curates 3576 experimentally verified MTIs between 657 miRNAs and 2297 target genes among 17 species. miRTarBase contains the largest amount of validated MTIs by comparing with other similar, previously developed databases. The MTIs collected in the miRTarBase can also provide a large amount of positive samples to develop computational methods capable of identifying miRNA–target interactions. miRTarBase is now available on http://miRTarBase.mbc.nctu.edu.tw/, and is updated frequently by continuously surveying research articles. Oxford University Press 2011-01 2010-11-10 /pmc/articles/PMC3013699/ /pubmed/21071411 http://dx.doi.org/10.1093/nar/gkq1107 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Hsu, Sheng-Da Lin, Feng-Mao Wu, Wei-Yun Liang, Chao Huang, Wei-Chih Chan, Wen-Ling Tsai, Wen-Ting Chen, Goun-Zhou Lee, Chia-Jung Chiu, Chih-Min Chien, Chia-Hung Wu, Ming-Chia Huang, Chi-Ying Tsou, Ann-Ping Huang, Hsien-Da miRTarBase: a database curates experimentally validated microRNA–target interactions |
title | miRTarBase: a database curates experimentally validated microRNA–target interactions |
title_full | miRTarBase: a database curates experimentally validated microRNA–target interactions |
title_fullStr | miRTarBase: a database curates experimentally validated microRNA–target interactions |
title_full_unstemmed | miRTarBase: a database curates experimentally validated microRNA–target interactions |
title_short | miRTarBase: a database curates experimentally validated microRNA–target interactions |
title_sort | mirtarbase: a database curates experimentally validated microrna–target interactions |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013699/ https://www.ncbi.nlm.nih.gov/pubmed/21071411 http://dx.doi.org/10.1093/nar/gkq1107 |
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