Cargando…
lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures
Attenuation of pre-rRNA synthesis in response to elevated temperature is accompanied by increased levels of PAPAS (“promoter and pre-rRNA antisense”), a long noncoding RNA (lncRNA) that is transcribed in an orientation antisense to pre-rRNA. Here we show that PAPAS interacts directly with DNA, formi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6049515/ https://www.ncbi.nlm.nih.gov/pubmed/29907651 http://dx.doi.org/10.1101/gad.311688.118 |
_version_ | 1783340230365937664 |
---|---|
author | Zhao, Zhongliang Sentürk, Nevcin Song, Chenlin Grummt, Ingrid |
author_facet | Zhao, Zhongliang Sentürk, Nevcin Song, Chenlin Grummt, Ingrid |
author_sort | Zhao, Zhongliang |
collection | PubMed |
description | Attenuation of pre-rRNA synthesis in response to elevated temperature is accompanied by increased levels of PAPAS (“promoter and pre-rRNA antisense”), a long noncoding RNA (lncRNA) that is transcribed in an orientation antisense to pre-rRNA. Here we show that PAPAS interacts directly with DNA, forming a DNA–RNA triplex structure that tethers PAPAS to a stretch of purines within the enhancer region, thereby guiding associated CHD4/NuRD (nucleosome remodeling and deacetylation) to the rDNA promoter. Protein–RNA interaction experiments combined with RNA secondary structure mapping revealed that the N-terminal part of CHD4 interacts with an unstructured A-rich region in PAPAS. Deletion or mutation of this sequence abolishes the interaction with CHD4. Stress-dependent up-regulation of PAPAS is accompanied by dephosphorylation of CHD4 at three serine residues, which enhances the interaction of CHD4/NuRD with RNA and reinforces repression of rDNA transcription. The results emphasize the function of lncRNAs in guiding chromatin remodeling complexes to specific genomic loci and uncover a phosphorylation-dependent mechanism of CHD4/NuRD-mediated transcriptional regulation. |
format | Online Article Text |
id | pubmed-6049515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60495152018-12-01 lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures Zhao, Zhongliang Sentürk, Nevcin Song, Chenlin Grummt, Ingrid Genes Dev Research Paper Attenuation of pre-rRNA synthesis in response to elevated temperature is accompanied by increased levels of PAPAS (“promoter and pre-rRNA antisense”), a long noncoding RNA (lncRNA) that is transcribed in an orientation antisense to pre-rRNA. Here we show that PAPAS interacts directly with DNA, forming a DNA–RNA triplex structure that tethers PAPAS to a stretch of purines within the enhancer region, thereby guiding associated CHD4/NuRD (nucleosome remodeling and deacetylation) to the rDNA promoter. Protein–RNA interaction experiments combined with RNA secondary structure mapping revealed that the N-terminal part of CHD4 interacts with an unstructured A-rich region in PAPAS. Deletion or mutation of this sequence abolishes the interaction with CHD4. Stress-dependent up-regulation of PAPAS is accompanied by dephosphorylation of CHD4 at three serine residues, which enhances the interaction of CHD4/NuRD with RNA and reinforces repression of rDNA transcription. The results emphasize the function of lncRNAs in guiding chromatin remodeling complexes to specific genomic loci and uncover a phosphorylation-dependent mechanism of CHD4/NuRD-mediated transcriptional regulation. Cold Spring Harbor Laboratory Press 2018-06-01 /pmc/articles/PMC6049515/ /pubmed/29907651 http://dx.doi.org/10.1101/gad.311688.118 Text en © 2018 Zhao et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Zhao, Zhongliang Sentürk, Nevcin Song, Chenlin Grummt, Ingrid lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title | lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title_full | lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title_fullStr | lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title_full_unstemmed | lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title_short | lncRNA PAPAS tethered to the rDNA enhancer recruits hypophosphorylated CHD4/NuRD to repress rRNA synthesis at elevated temperatures |
title_sort | lncrna papas tethered to the rdna enhancer recruits hypophosphorylated chd4/nurd to repress rrna synthesis at elevated temperatures |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6049515/ https://www.ncbi.nlm.nih.gov/pubmed/29907651 http://dx.doi.org/10.1101/gad.311688.118 |
work_keys_str_mv | AT zhaozhongliang lncrnapapastetheredtotherdnaenhancerrecruitshypophosphorylatedchd4nurdtorepressrrnasynthesisatelevatedtemperatures AT senturknevcin lncrnapapastetheredtotherdnaenhancerrecruitshypophosphorylatedchd4nurdtorepressrrnasynthesisatelevatedtemperatures AT songchenlin lncrnapapastetheredtotherdnaenhancerrecruitshypophosphorylatedchd4nurdtorepressrrnasynthesisatelevatedtemperatures AT grummtingrid lncrnapapastetheredtotherdnaenhancerrecruitshypophosphorylatedchd4nurdtorepressrrnasynthesisatelevatedtemperatures |