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Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model
Hidden Markov models (HMMs) have been extensively used to dissect the genome into functionally distinct regions using data such as RNA expression or DNA binding measurements. It is a challenge to disentangle processes occurring on complementary strands of the same genomic region. We present the doub...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797261/ https://www.ncbi.nlm.nih.gov/pubmed/26578558 http://dx.doi.org/10.1093/nar/gkv1184 |
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author | Glas, Julia Dümcke, Sebastian Zacher, Benedikt Poron, Don Gagneur, Julien Tresch, Achim |
author_facet | Glas, Julia Dümcke, Sebastian Zacher, Benedikt Poron, Don Gagneur, Julien Tresch, Achim |
author_sort | Glas, Julia |
collection | PubMed |
description | Hidden Markov models (HMMs) have been extensively used to dissect the genome into functionally distinct regions using data such as RNA expression or DNA binding measurements. It is a challenge to disentangle processes occurring on complementary strands of the same genomic region. We present the double-stranded HMM (dsHMM), a model for the strand-specific analysis of genomic processes. We applied dsHMM to yeast using strand specific transcription data, nucleosome data, and protein binding data for a set of 11 factors associated with the regulation of transcription.The resulting annotation recovers the mRNA transcription cycle (initiation, elongation, termination) while correctly predicting strand-specificity and directionality of the transcription process. We find that pre-initiation complex formation is an essentially undirected process, giving rise to a large number of bidirectional promoters and to pervasive antisense transcription. Notably, 12% of all transcriptionally active positions showed simultaneous activity on both strands. Furthermore, dsHMM reveals that antisense transcription is specifically suppressed by Nrd1, a yeast termination factor. |
format | Online Article Text |
id | pubmed-4797261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47972612016-03-21 Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model Glas, Julia Dümcke, Sebastian Zacher, Benedikt Poron, Don Gagneur, Julien Tresch, Achim Nucleic Acids Res Methods Online Hidden Markov models (HMMs) have been extensively used to dissect the genome into functionally distinct regions using data such as RNA expression or DNA binding measurements. It is a challenge to disentangle processes occurring on complementary strands of the same genomic region. We present the double-stranded HMM (dsHMM), a model for the strand-specific analysis of genomic processes. We applied dsHMM to yeast using strand specific transcription data, nucleosome data, and protein binding data for a set of 11 factors associated with the regulation of transcription.The resulting annotation recovers the mRNA transcription cycle (initiation, elongation, termination) while correctly predicting strand-specificity and directionality of the transcription process. We find that pre-initiation complex formation is an essentially undirected process, giving rise to a large number of bidirectional promoters and to pervasive antisense transcription. Notably, 12% of all transcriptionally active positions showed simultaneous activity on both strands. Furthermore, dsHMM reveals that antisense transcription is specifically suppressed by Nrd1, a yeast termination factor. Oxford University Press 2016-03-18 2015-11-17 /pmc/articles/PMC4797261/ /pubmed/26578558 http://dx.doi.org/10.1093/nar/gkv1184 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Glas, Julia Dümcke, Sebastian Zacher, Benedikt Poron, Don Gagneur, Julien Tresch, Achim Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title | Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title_full | Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title_fullStr | Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title_full_unstemmed | Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title_short | Simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden Markov model |
title_sort | simultaneous characterization of sense and antisense genomic processes by the double-stranded hidden markov model |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797261/ https://www.ncbi.nlm.nih.gov/pubmed/26578558 http://dx.doi.org/10.1093/nar/gkv1184 |
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