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POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins
RNA-binding proteins (RBPs) play key roles in post-transcriptional regulation. Accurate identification of RBP binding sites in multiple cell lines and tissue types from diverse species is a fundamental endeavor towards understanding the regulatory mechanisms of RBPs under both physiological and path...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728292/ https://www.ncbi.nlm.nih.gov/pubmed/34403477 http://dx.doi.org/10.1093/nar/gkab702 |
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author | Zhao, Weihao Zhang, Shang Zhu, Yumin Xi, Xiaochen Bao, Pengfei Ma, Ziyuan Kapral, Thomas H Chen, Shuyuan Zagrovic, Bojan Yang, Yucheng T Lu, Zhi John |
author_facet | Zhao, Weihao Zhang, Shang Zhu, Yumin Xi, Xiaochen Bao, Pengfei Ma, Ziyuan Kapral, Thomas H Chen, Shuyuan Zagrovic, Bojan Yang, Yucheng T Lu, Zhi John |
author_sort | Zhao, Weihao |
collection | PubMed |
description | RNA-binding proteins (RBPs) play key roles in post-transcriptional regulation. Accurate identification of RBP binding sites in multiple cell lines and tissue types from diverse species is a fundamental endeavor towards understanding the regulatory mechanisms of RBPs under both physiological and pathological conditions. Our POSTAR annotation processes make use of publicly available large-scale CLIP-seq datasets and external functional genomic annotations to generate a comprehensive map of RBP binding sites and their association with other regulatory events as well as functional variants. Here, we present POSTAR3, an updated database with improvements in data collection, annotation infrastructure, and analysis that support the annotation of post-transcriptional regulation in multiple species including: we made a comprehensive update on the CLIP-seq and Ribo-seq datasets which cover more biological conditions, technologies, and species; we added RNA secondary structure profiling for RBP binding sites; we provided miRNA-mediated degradation events validated by degradome-seq; we included RBP binding sites at circRNA junction regions; we expanded the annotation of RBP binding sites, particularly using updated genomic variants and mutations associated with diseases. POSTAR3 is freely available at http://postar.ncrnalab.org. |
format | Online Article Text |
id | pubmed-8728292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87282922022-01-05 POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins Zhao, Weihao Zhang, Shang Zhu, Yumin Xi, Xiaochen Bao, Pengfei Ma, Ziyuan Kapral, Thomas H Chen, Shuyuan Zagrovic, Bojan Yang, Yucheng T Lu, Zhi John Nucleic Acids Res Database Issue RNA-binding proteins (RBPs) play key roles in post-transcriptional regulation. Accurate identification of RBP binding sites in multiple cell lines and tissue types from diverse species is a fundamental endeavor towards understanding the regulatory mechanisms of RBPs under both physiological and pathological conditions. Our POSTAR annotation processes make use of publicly available large-scale CLIP-seq datasets and external functional genomic annotations to generate a comprehensive map of RBP binding sites and their association with other regulatory events as well as functional variants. Here, we present POSTAR3, an updated database with improvements in data collection, annotation infrastructure, and analysis that support the annotation of post-transcriptional regulation in multiple species including: we made a comprehensive update on the CLIP-seq and Ribo-seq datasets which cover more biological conditions, technologies, and species; we added RNA secondary structure profiling for RBP binding sites; we provided miRNA-mediated degradation events validated by degradome-seq; we included RBP binding sites at circRNA junction regions; we expanded the annotation of RBP binding sites, particularly using updated genomic variants and mutations associated with diseases. POSTAR3 is freely available at http://postar.ncrnalab.org. Oxford University Press 2021-08-17 /pmc/articles/PMC8728292/ /pubmed/34403477 http://dx.doi.org/10.1093/nar/gkab702 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Issue Zhao, Weihao Zhang, Shang Zhu, Yumin Xi, Xiaochen Bao, Pengfei Ma, Ziyuan Kapral, Thomas H Chen, Shuyuan Zagrovic, Bojan Yang, Yucheng T Lu, Zhi John POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title | POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title_full | POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title_fullStr | POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title_full_unstemmed | POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title_short | POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins |
title_sort | postar3: an updated platform for exploring post-transcriptional regulation coordinated by rna-binding proteins |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728292/ https://www.ncbi.nlm.nih.gov/pubmed/34403477 http://dx.doi.org/10.1093/nar/gkab702 |
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