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Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis
Piwi-interacting RNAs (piRNAs) are important for genome regulation across metazoans, but their biogenesis evolves rapidly. In Caenorhabditis elegans, piRNA loci are clustered within two 3-Mb regions on chromosome IV. Each piRNA locus possesses an upstream motif that recruits RNA polymerase II to pro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436959/ https://www.ncbi.nlm.nih.gov/pubmed/30713076 http://dx.doi.org/10.1016/j.devcel.2018.12.026 |
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author | Beltran, Toni Barroso, Consuelo Birkle, Timothy Y. Stevens, Lewis Schwartz, Hillel T. Sternberg, Paul W. Fradin, Hélène Gunsalus, Kristin Piano, Fabio Sharma, Garima Cerrato, Chiara Ahringer, Julie Martínez-Pérez, Enrique Blaxter, Mark Sarkies, Peter |
author_facet | Beltran, Toni Barroso, Consuelo Birkle, Timothy Y. Stevens, Lewis Schwartz, Hillel T. Sternberg, Paul W. Fradin, Hélène Gunsalus, Kristin Piano, Fabio Sharma, Garima Cerrato, Chiara Ahringer, Julie Martínez-Pérez, Enrique Blaxter, Mark Sarkies, Peter |
author_sort | Beltran, Toni |
collection | PubMed |
description | Piwi-interacting RNAs (piRNAs) are important for genome regulation across metazoans, but their biogenesis evolves rapidly. In Caenorhabditis elegans, piRNA loci are clustered within two 3-Mb regions on chromosome IV. Each piRNA locus possesses an upstream motif that recruits RNA polymerase II to produce an ∼28 nt primary transcript. We used comparative epigenomics across nematodes to gain insight into the origin, evolution, and mechanism of nematode piRNA biogenesis. We show that the piRNA upstream motif is derived from core promoter elements controlling snRNA transcription. We describe two alternative modes of piRNA organization in nematodes: in C. elegans and closely related nematodes, piRNAs are clustered within repressive H3K27me3 chromatin, while in other species, typified by Pristionchus pacificus, piRNAs are found within introns of active genes. Additionally, we discover that piRNA production depends on sequence signals associated with RNA polymerase II pausing. We show that pausing signals synergize with chromatin to control piRNA transcription. |
format | Online Article Text |
id | pubmed-6436959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64369592019-04-10 Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis Beltran, Toni Barroso, Consuelo Birkle, Timothy Y. Stevens, Lewis Schwartz, Hillel T. Sternberg, Paul W. Fradin, Hélène Gunsalus, Kristin Piano, Fabio Sharma, Garima Cerrato, Chiara Ahringer, Julie Martínez-Pérez, Enrique Blaxter, Mark Sarkies, Peter Dev Cell Article Piwi-interacting RNAs (piRNAs) are important for genome regulation across metazoans, but their biogenesis evolves rapidly. In Caenorhabditis elegans, piRNA loci are clustered within two 3-Mb regions on chromosome IV. Each piRNA locus possesses an upstream motif that recruits RNA polymerase II to produce an ∼28 nt primary transcript. We used comparative epigenomics across nematodes to gain insight into the origin, evolution, and mechanism of nematode piRNA biogenesis. We show that the piRNA upstream motif is derived from core promoter elements controlling snRNA transcription. We describe two alternative modes of piRNA organization in nematodes: in C. elegans and closely related nematodes, piRNAs are clustered within repressive H3K27me3 chromatin, while in other species, typified by Pristionchus pacificus, piRNAs are found within introns of active genes. Additionally, we discover that piRNA production depends on sequence signals associated with RNA polymerase II pausing. We show that pausing signals synergize with chromatin to control piRNA transcription. Cell Press 2019-03-25 /pmc/articles/PMC6436959/ /pubmed/30713076 http://dx.doi.org/10.1016/j.devcel.2018.12.026 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Beltran, Toni Barroso, Consuelo Birkle, Timothy Y. Stevens, Lewis Schwartz, Hillel T. Sternberg, Paul W. Fradin, Hélène Gunsalus, Kristin Piano, Fabio Sharma, Garima Cerrato, Chiara Ahringer, Julie Martínez-Pérez, Enrique Blaxter, Mark Sarkies, Peter Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title | Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title_full | Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title_fullStr | Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title_full_unstemmed | Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title_short | Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis |
title_sort | comparative epigenomics reveals that rna polymerase ii pausing and chromatin domain organization control nematode pirna biogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436959/ https://www.ncbi.nlm.nih.gov/pubmed/30713076 http://dx.doi.org/10.1016/j.devcel.2018.12.026 |
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