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CirGRDB: a database for the genome-wide deciphering circadian genes and regulators
Circadian rhythms govern various kinds of physiological and behavioral functions of the living organisms, and disruptions of the rhythms are highly detrimental to health. Although several databases have been built for circadian genes, a resource for comprehensive post-transcriptional regulatory info...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753205/ https://www.ncbi.nlm.nih.gov/pubmed/29059379 http://dx.doi.org/10.1093/nar/gkx944 |
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author | Li, Xianfeng Shi, Leisheng Zhang, Kun Wei, Wenqing Liu, Qi Mao, Fengbiao Li, Jinchen Cai, Wanshi Chen, Huiqian Teng, Huajing Li, Jiada Sun, Zhongsheng |
author_facet | Li, Xianfeng Shi, Leisheng Zhang, Kun Wei, Wenqing Liu, Qi Mao, Fengbiao Li, Jinchen Cai, Wanshi Chen, Huiqian Teng, Huajing Li, Jiada Sun, Zhongsheng |
author_sort | Li, Xianfeng |
collection | PubMed |
description | Circadian rhythms govern various kinds of physiological and behavioral functions of the living organisms, and disruptions of the rhythms are highly detrimental to health. Although several databases have been built for circadian genes, a resource for comprehensive post-transcriptional regulatory information of circadian RNAs and expression patterns of disease-related circadian RNAs is still lacking. Here, we developed CirGRDB (http://cirgrdb.biols.ac.cn) by integrating more than 4936 genome-wide assays, with the aim of fulfilling the growing need to understand the rhythms of life. CirGRDB presents a friendly web interface that allows users to search and browse temporal expression patterns of interested genes in 37 human/mouse tissues or cell lines, and three clinical disorders including sleep disorder, aging and tumor. More importantly, eight kinds of potential transcriptional and post-transcriptional regulators involved in the rhythmic expression of the specific genes, including transcription factors, histone modifications, chromatin accessibility, enhancer RNAs, miRNAs, RNA-binding proteins, RNA editing and RNA methylation, can also be retrieved. Furthermore, a regulatory network could be generated based on the regulatory information. In summary, CirGRDB offers a useful repository for exploring disease-related circadian RNAs, and deciphering the transcriptional and post-transcriptional regulation of circadian rhythms. |
format | Online Article Text |
id | pubmed-5753205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57532052018-01-05 CirGRDB: a database for the genome-wide deciphering circadian genes and regulators Li, Xianfeng Shi, Leisheng Zhang, Kun Wei, Wenqing Liu, Qi Mao, Fengbiao Li, Jinchen Cai, Wanshi Chen, Huiqian Teng, Huajing Li, Jiada Sun, Zhongsheng Nucleic Acids Res Database Issue Circadian rhythms govern various kinds of physiological and behavioral functions of the living organisms, and disruptions of the rhythms are highly detrimental to health. Although several databases have been built for circadian genes, a resource for comprehensive post-transcriptional regulatory information of circadian RNAs and expression patterns of disease-related circadian RNAs is still lacking. Here, we developed CirGRDB (http://cirgrdb.biols.ac.cn) by integrating more than 4936 genome-wide assays, with the aim of fulfilling the growing need to understand the rhythms of life. CirGRDB presents a friendly web interface that allows users to search and browse temporal expression patterns of interested genes in 37 human/mouse tissues or cell lines, and three clinical disorders including sleep disorder, aging and tumor. More importantly, eight kinds of potential transcriptional and post-transcriptional regulators involved in the rhythmic expression of the specific genes, including transcription factors, histone modifications, chromatin accessibility, enhancer RNAs, miRNAs, RNA-binding proteins, RNA editing and RNA methylation, can also be retrieved. Furthermore, a regulatory network could be generated based on the regulatory information. In summary, CirGRDB offers a useful repository for exploring disease-related circadian RNAs, and deciphering the transcriptional and post-transcriptional regulation of circadian rhythms. Oxford University Press 2018-01-04 2017-10-20 /pmc/articles/PMC5753205/ /pubmed/29059379 http://dx.doi.org/10.1093/nar/gkx944 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Li, Xianfeng Shi, Leisheng Zhang, Kun Wei, Wenqing Liu, Qi Mao, Fengbiao Li, Jinchen Cai, Wanshi Chen, Huiqian Teng, Huajing Li, Jiada Sun, Zhongsheng CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title | CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title_full | CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title_fullStr | CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title_full_unstemmed | CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title_short | CirGRDB: a database for the genome-wide deciphering circadian genes and regulators |
title_sort | cirgrdb: a database for the genome-wide deciphering circadian genes and regulators |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753205/ https://www.ncbi.nlm.nih.gov/pubmed/29059379 http://dx.doi.org/10.1093/nar/gkx944 |
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