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R-Loops Promote Antisense Transcription across the Mammalian Genome
Widespread antisense long noncoding RNA (lncRNA) overlap with many protein-coding genes in mammals and emanate from gene promoter, enhancer, and termination regions. However, their origin and biological purpose remain unclear. We show that these antisense lncRNA can be generated by R-loops that form...
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/PMC6868509/ https://www.ncbi.nlm.nih.gov/pubmed/31679819 http://dx.doi.org/10.1016/j.molcel.2019.10.002 |
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author | Tan-Wong, Sue Mei Dhir, Somdutta Proudfoot, Nick J. |
author_facet | Tan-Wong, Sue Mei Dhir, Somdutta Proudfoot, Nick J. |
author_sort | Tan-Wong, Sue Mei |
collection | PubMed |
description | Widespread antisense long noncoding RNA (lncRNA) overlap with many protein-coding genes in mammals and emanate from gene promoter, enhancer, and termination regions. However, their origin and biological purpose remain unclear. We show that these antisense lncRNA can be generated by R-loops that form when nascent transcript invades the DNA duplex behind elongating RNA polymerase II (Pol II). Biochemically, R-loops act as intrinsic Pol II promoters to induce de novo RNA synthesis. Furthermore, their removal across the human genome by RNase H1 overexpression causes the selective reduction of antisense transcription. Consequently, we predict that R-loops act to facilitate the synthesis of many gene proximal antisense lncRNA. Not only are R-loops widely associated with DNA damage and repair, but we now show that they have the capacity to promote de novo transcript synthesis that may have aided the evolution of gene regulation. |
format | Online Article Text |
id | pubmed-6868509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68685092019-11-25 R-Loops Promote Antisense Transcription across the Mammalian Genome Tan-Wong, Sue Mei Dhir, Somdutta Proudfoot, Nick J. Mol Cell Article Widespread antisense long noncoding RNA (lncRNA) overlap with many protein-coding genes in mammals and emanate from gene promoter, enhancer, and termination regions. However, their origin and biological purpose remain unclear. We show that these antisense lncRNA can be generated by R-loops that form when nascent transcript invades the DNA duplex behind elongating RNA polymerase II (Pol II). Biochemically, R-loops act as intrinsic Pol II promoters to induce de novo RNA synthesis. Furthermore, their removal across the human genome by RNase H1 overexpression causes the selective reduction of antisense transcription. Consequently, we predict that R-loops act to facilitate the synthesis of many gene proximal antisense lncRNA. Not only are R-loops widely associated with DNA damage and repair, but we now show that they have the capacity to promote de novo transcript synthesis that may have aided the evolution of gene regulation. Cell Press 2019-11-21 /pmc/articles/PMC6868509/ /pubmed/31679819 http://dx.doi.org/10.1016/j.molcel.2019.10.002 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 Tan-Wong, Sue Mei Dhir, Somdutta Proudfoot, Nick J. R-Loops Promote Antisense Transcription across the Mammalian Genome |
title | R-Loops Promote Antisense Transcription across the Mammalian Genome |
title_full | R-Loops Promote Antisense Transcription across the Mammalian Genome |
title_fullStr | R-Loops Promote Antisense Transcription across the Mammalian Genome |
title_full_unstemmed | R-Loops Promote Antisense Transcription across the Mammalian Genome |
title_short | R-Loops Promote Antisense Transcription across the Mammalian Genome |
title_sort | r-loops promote antisense transcription across the mammalian genome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868509/ https://www.ncbi.nlm.nih.gov/pubmed/31679819 http://dx.doi.org/10.1016/j.molcel.2019.10.002 |
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