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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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.
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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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