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APADB: a database for alternative polyadenylation and microRNA regulation events

Alternative polyadenylation (APA) is a widespread mechanism that contributes to the sophisticated dynamics of gene regulation. Approximately 50% of all protein-coding human genes harbor multiple polyadenylation (PA) sites; their selective and combinatorial use gives rise to transcript variants with...

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Autores principales: Müller, Sören, Rycak, Lukas, Afonso-Grunz, Fabian, Winter, Peter, Zawada, Adam M., Damrath, Ewa, Scheider, Jessica, Schmäh, Juliane, Koch, Ina, Kahl, Günter, Rotter, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105710/
https://www.ncbi.nlm.nih.gov/pubmed/25052703
http://dx.doi.org/10.1093/database/bau076
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author Müller, Sören
Rycak, Lukas
Afonso-Grunz, Fabian
Winter, Peter
Zawada, Adam M.
Damrath, Ewa
Scheider, Jessica
Schmäh, Juliane
Koch, Ina
Kahl, Günter
Rotter, Björn
author_facet Müller, Sören
Rycak, Lukas
Afonso-Grunz, Fabian
Winter, Peter
Zawada, Adam M.
Damrath, Ewa
Scheider, Jessica
Schmäh, Juliane
Koch, Ina
Kahl, Günter
Rotter, Björn
author_sort Müller, Sören
collection PubMed
description Alternative polyadenylation (APA) is a widespread mechanism that contributes to the sophisticated dynamics of gene regulation. Approximately 50% of all protein-coding human genes harbor multiple polyadenylation (PA) sites; their selective and combinatorial use gives rise to transcript variants with differing length of their 3′ untranslated region (3′UTR). Shortened variants escape UTR-mediated regulation by microRNAs (miRNAs), especially in cancer, where global 3′UTR shortening accelerates disease progression, dedifferentiation and proliferation. Here we present APADB, a database of vertebrate PA sites determined by 3′ end sequencing, using massive analysis of complementary DNA ends. APADB provides (A)PA sites for coding and non-coding transcripts of human, mouse and chicken genes. For human and mouse, several tissue types, including different cancer specimens, are available. APADB records the loss of predicted miRNA binding sites and visualizes next-generation sequencing reads that support each PA site in a genome browser. The database tables can either be browsed according to organism and tissue or alternatively searched for a gene of interest. APADB is the largest database of APA in human, chicken and mouse. The stored information provides experimental evidence for thousands of PA sites and APA events. APADB combines 3′ end sequencing data with prediction algorithms of miRNA binding sites, allowing to further improve prediction algorithms. Current databases lack correct information about 3′UTR lengths, especially for chicken, and APADB provides necessary information to close this gap. Database URL: http://tools.genxpro.net/apadb/
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spelling pubmed-41057102014-07-23 APADB: a database for alternative polyadenylation and microRNA regulation events Müller, Sören Rycak, Lukas Afonso-Grunz, Fabian Winter, Peter Zawada, Adam M. Damrath, Ewa Scheider, Jessica Schmäh, Juliane Koch, Ina Kahl, Günter Rotter, Björn Database (Oxford) Original Article Alternative polyadenylation (APA) is a widespread mechanism that contributes to the sophisticated dynamics of gene regulation. Approximately 50% of all protein-coding human genes harbor multiple polyadenylation (PA) sites; their selective and combinatorial use gives rise to transcript variants with differing length of their 3′ untranslated region (3′UTR). Shortened variants escape UTR-mediated regulation by microRNAs (miRNAs), especially in cancer, where global 3′UTR shortening accelerates disease progression, dedifferentiation and proliferation. Here we present APADB, a database of vertebrate PA sites determined by 3′ end sequencing, using massive analysis of complementary DNA ends. APADB provides (A)PA sites for coding and non-coding transcripts of human, mouse and chicken genes. For human and mouse, several tissue types, including different cancer specimens, are available. APADB records the loss of predicted miRNA binding sites and visualizes next-generation sequencing reads that support each PA site in a genome browser. The database tables can either be browsed according to organism and tissue or alternatively searched for a gene of interest. APADB is the largest database of APA in human, chicken and mouse. The stored information provides experimental evidence for thousands of PA sites and APA events. APADB combines 3′ end sequencing data with prediction algorithms of miRNA binding sites, allowing to further improve prediction algorithms. Current databases lack correct information about 3′UTR lengths, especially for chicken, and APADB provides necessary information to close this gap. Database URL: http://tools.genxpro.net/apadb/ Oxford University Press 2014-07-21 /pmc/articles/PMC4105710/ /pubmed/25052703 http://dx.doi.org/10.1093/database/bau076 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Müller, Sören
Rycak, Lukas
Afonso-Grunz, Fabian
Winter, Peter
Zawada, Adam M.
Damrath, Ewa
Scheider, Jessica
Schmäh, Juliane
Koch, Ina
Kahl, Günter
Rotter, Björn
APADB: a database for alternative polyadenylation and microRNA regulation events
title APADB: a database for alternative polyadenylation and microRNA regulation events
title_full APADB: a database for alternative polyadenylation and microRNA regulation events
title_fullStr APADB: a database for alternative polyadenylation and microRNA regulation events
title_full_unstemmed APADB: a database for alternative polyadenylation and microRNA regulation events
title_short APADB: a database for alternative polyadenylation and microRNA regulation events
title_sort apadb: a database for alternative polyadenylation and microrna regulation events
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105710/
https://www.ncbi.nlm.nih.gov/pubmed/25052703
http://dx.doi.org/10.1093/database/bau076
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