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Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data
BACKGROUND: MicroRNAs (miRNAs) are short, non-coding RNA regulators of protein coding genes. miRNAs play a very important role in diverse biological processes and various diseases. Many algorithms are able to predict miRNA genes and their targets, but their transcription regulation is still under in...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668758/ https://www.ncbi.nlm.nih.gov/pubmed/19390574 http://dx.doi.org/10.1371/journal.pone.0005279 |
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author | Corcoran, David L. Pandit, Kusum V. Gordon, Ben Bhattacharjee, Arindam Kaminski, Naftali Benos, Panayiotis V. |
author_facet | Corcoran, David L. Pandit, Kusum V. Gordon, Ben Bhattacharjee, Arindam Kaminski, Naftali Benos, Panayiotis V. |
author_sort | Corcoran, David L. |
collection | PubMed |
description | BACKGROUND: MicroRNAs (miRNAs) are short, non-coding RNA regulators of protein coding genes. miRNAs play a very important role in diverse biological processes and various diseases. Many algorithms are able to predict miRNA genes and their targets, but their transcription regulation is still under investigation. It is generally believed that intragenic miRNAs (located in introns or exons of protein coding genes) are co-transcribed with their host genes and most intergenic miRNAs transcribed from their own RNA polymerase II (Pol II) promoter. However, the length of the primary transcripts and promoter organization is currently unknown. METHODOLOGY: We performed Pol II chromatin immunoprecipitation (ChIP)-chip using a custom array surrounding regions of known miRNA genes. To identify the true core transcription start sites of the miRNA genes we developed a new tool (CPPP). We showed that miRNA genes can be transcribed from promoters located several kilobases away and that their promoters share the same general features as those of protein coding genes. Finally, we found evidence that as many as 26% of the intragenic miRNAs may be transcribed from their own unique promoters. CONCLUSION: miRNA promoters have similar features to those of protein coding genes, but miRNA transcript organization is more complex. |
format | Text |
id | pubmed-2668758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26687582009-04-23 Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data Corcoran, David L. Pandit, Kusum V. Gordon, Ben Bhattacharjee, Arindam Kaminski, Naftali Benos, Panayiotis V. PLoS One Research Article BACKGROUND: MicroRNAs (miRNAs) are short, non-coding RNA regulators of protein coding genes. miRNAs play a very important role in diverse biological processes and various diseases. Many algorithms are able to predict miRNA genes and their targets, but their transcription regulation is still under investigation. It is generally believed that intragenic miRNAs (located in introns or exons of protein coding genes) are co-transcribed with their host genes and most intergenic miRNAs transcribed from their own RNA polymerase II (Pol II) promoter. However, the length of the primary transcripts and promoter organization is currently unknown. METHODOLOGY: We performed Pol II chromatin immunoprecipitation (ChIP)-chip using a custom array surrounding regions of known miRNA genes. To identify the true core transcription start sites of the miRNA genes we developed a new tool (CPPP). We showed that miRNA genes can be transcribed from promoters located several kilobases away and that their promoters share the same general features as those of protein coding genes. Finally, we found evidence that as many as 26% of the intragenic miRNAs may be transcribed from their own unique promoters. CONCLUSION: miRNA promoters have similar features to those of protein coding genes, but miRNA transcript organization is more complex. Public Library of Science 2009-04-23 /pmc/articles/PMC2668758/ /pubmed/19390574 http://dx.doi.org/10.1371/journal.pone.0005279 Text en Corcoran et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Corcoran, David L. Pandit, Kusum V. Gordon, Ben Bhattacharjee, Arindam Kaminski, Naftali Benos, Panayiotis V. Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title | Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title_full | Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title_fullStr | Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title_full_unstemmed | Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title_short | Features of Mammalian microRNA Promoters Emerge from Polymerase II Chromatin Immunoprecipitation Data |
title_sort | features of mammalian microrna promoters emerge from polymerase ii chromatin immunoprecipitation data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668758/ https://www.ncbi.nlm.nih.gov/pubmed/19390574 http://dx.doi.org/10.1371/journal.pone.0005279 |
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