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DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs
Deregulation of microRNA (miRNA) expression plays a critical role in the transition from a physiological to a pathological state. The accurate miRNA promoter identification in multiple cell types is a fundamental endeavor towards understanding and characterizing the underlying mechanisms of both phy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778932/ https://www.ncbi.nlm.nih.gov/pubmed/33245765 http://dx.doi.org/10.1093/nar/gkaa1060 |
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author | Perdikopanis, Nikos Georgakilas, Georgios K Grigoriadis, Dimitris Pierros, Vasilis Kavakiotis, Ioannis Alexiou, Panagiotis Hatzigeorgiou, Artemis |
author_facet | Perdikopanis, Nikos Georgakilas, Georgios K Grigoriadis, Dimitris Pierros, Vasilis Kavakiotis, Ioannis Alexiou, Panagiotis Hatzigeorgiou, Artemis |
author_sort | Perdikopanis, Nikos |
collection | PubMed |
description | Deregulation of microRNA (miRNA) expression plays a critical role in the transition from a physiological to a pathological state. The accurate miRNA promoter identification in multiple cell types is a fundamental endeavor towards understanding and characterizing the underlying mechanisms of both physiological as well as pathological conditions. DIANA-miRGen v4 (www.microrna.gr/mirgenv4) provides cell type specific miRNA transcription start sites (TSSs) for over 1500 miRNAs retrieved from the analysis of >1000 cap analysis of gene expression (CAGE) samples corresponding to 133 tissues, cell lines and primary cells available in FANTOM repository. MiRNA TSS locations were associated with transcription factor binding site (TFBSs) annotation, for >280 TFs, derived from analyzing the majority of ENCODE ChIP-Seq datasets. For the first time, clusters of cell types having common miRNA TSSs are characterized and provided through a user friendly interface with multiple layers of customization. DIANA-miRGen v4 significantly improves our understanding of miRNA biogenesis regulation at the transcriptional level by providing a unique integration of high-quality annotations for hundreds of cell specific miRNA promoters with experimentally derived TFBSs. |
format | Online Article Text |
id | pubmed-7778932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77789322021-01-06 DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs Perdikopanis, Nikos Georgakilas, Georgios K Grigoriadis, Dimitris Pierros, Vasilis Kavakiotis, Ioannis Alexiou, Panagiotis Hatzigeorgiou, Artemis Nucleic Acids Res Database Issue Deregulation of microRNA (miRNA) expression plays a critical role in the transition from a physiological to a pathological state. The accurate miRNA promoter identification in multiple cell types is a fundamental endeavor towards understanding and characterizing the underlying mechanisms of both physiological as well as pathological conditions. DIANA-miRGen v4 (www.microrna.gr/mirgenv4) provides cell type specific miRNA transcription start sites (TSSs) for over 1500 miRNAs retrieved from the analysis of >1000 cap analysis of gene expression (CAGE) samples corresponding to 133 tissues, cell lines and primary cells available in FANTOM repository. MiRNA TSS locations were associated with transcription factor binding site (TFBSs) annotation, for >280 TFs, derived from analyzing the majority of ENCODE ChIP-Seq datasets. For the first time, clusters of cell types having common miRNA TSSs are characterized and provided through a user friendly interface with multiple layers of customization. DIANA-miRGen v4 significantly improves our understanding of miRNA biogenesis regulation at the transcriptional level by providing a unique integration of high-quality annotations for hundreds of cell specific miRNA promoters with experimentally derived TFBSs. Oxford University Press 2020-11-27 /pmc/articles/PMC7778932/ /pubmed/33245765 http://dx.doi.org/10.1093/nar/gkaa1060 Text en © The Author(s) 2020. 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 Non-Commercial 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 Perdikopanis, Nikos Georgakilas, Georgios K Grigoriadis, Dimitris Pierros, Vasilis Kavakiotis, Ioannis Alexiou, Panagiotis Hatzigeorgiou, Artemis DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title | DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title_full | DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title_fullStr | DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title_full_unstemmed | DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title_short | DIANA-miRGen v4: indexing promoters and regulators for more than 1500 microRNAs |
title_sort | diana-mirgen v4: indexing promoters and regulators for more than 1500 micrornas |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778932/ https://www.ncbi.nlm.nih.gov/pubmed/33245765 http://dx.doi.org/10.1093/nar/gkaa1060 |
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