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Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans
Eukaryotic cells express a wide variety of endogenous small regulatory RNAs that function in the nucleus. We previously found that erroneous rRNAs induce the generation of antisense ribosomal siRNAs (risiRNAs) which silence the expression of rRNAs via the nuclear RNAi defective (Nrde) pathway. To fu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450093/ https://www.ncbi.nlm.nih.gov/pubmed/34365510 http://dx.doi.org/10.1093/nar/gkab662 |
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author | Liao, Shimiao Chen, Xiangyang Xu, Ting Jin, Qile Xu, Zongxiu Xu, Demin Zhou, Xufei Zhu, Chengming Guang, Shouhong Feng, Xuezhu |
author_facet | Liao, Shimiao Chen, Xiangyang Xu, Ting Jin, Qile Xu, Zongxiu Xu, Demin Zhou, Xufei Zhu, Chengming Guang, Shouhong Feng, Xuezhu |
author_sort | Liao, Shimiao |
collection | PubMed |
description | Eukaryotic cells express a wide variety of endogenous small regulatory RNAs that function in the nucleus. We previously found that erroneous rRNAs induce the generation of antisense ribosomal siRNAs (risiRNAs) which silence the expression of rRNAs via the nuclear RNAi defective (Nrde) pathway. To further understand the biological roles and mechanisms of this class of small regulatory RNAs, we conducted forward genetic screening to identify factors involved in risiRNA generation in Caenorhabditis elegans. We found that risiRNAs accumulated in the RNA exosome mutants. risiRNAs directed the association of NRDE proteins with pre-rRNAs and the silencing of pre-rRNAs. In the presence of risiRNAs, NRDE-2 accumulated in the nucleolus and colocalized with RNA polymerase I. risiRNAs inhibited the transcription elongation of RNA polymerase I by decreasing RNAP I occupancy downstream of the RNAi-targeted site. Meanwhile, exosomes mislocalized from the nucleolus to nucleoplasm in suppressor of siRNA (susi) mutants, in which erroneous rRNAs accumulated. These results established a novel model of rRNA surveillance by combining ribonuclease-mediated RNA degradation with small RNA-directed nucleolar RNAi system. |
format | Online Article Text |
id | pubmed-8450093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84500932021-09-20 Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans Liao, Shimiao Chen, Xiangyang Xu, Ting Jin, Qile Xu, Zongxiu Xu, Demin Zhou, Xufei Zhu, Chengming Guang, Shouhong Feng, Xuezhu Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Eukaryotic cells express a wide variety of endogenous small regulatory RNAs that function in the nucleus. We previously found that erroneous rRNAs induce the generation of antisense ribosomal siRNAs (risiRNAs) which silence the expression of rRNAs via the nuclear RNAi defective (Nrde) pathway. To further understand the biological roles and mechanisms of this class of small regulatory RNAs, we conducted forward genetic screening to identify factors involved in risiRNA generation in Caenorhabditis elegans. We found that risiRNAs accumulated in the RNA exosome mutants. risiRNAs directed the association of NRDE proteins with pre-rRNAs and the silencing of pre-rRNAs. In the presence of risiRNAs, NRDE-2 accumulated in the nucleolus and colocalized with RNA polymerase I. risiRNAs inhibited the transcription elongation of RNA polymerase I by decreasing RNAP I occupancy downstream of the RNAi-targeted site. Meanwhile, exosomes mislocalized from the nucleolus to nucleoplasm in suppressor of siRNA (susi) mutants, in which erroneous rRNAs accumulated. These results established a novel model of rRNA surveillance by combining ribonuclease-mediated RNA degradation with small RNA-directed nucleolar RNAi system. Oxford University Press 2021-08-07 /pmc/articles/PMC8450093/ /pubmed/34365510 http://dx.doi.org/10.1093/nar/gkab662 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Liao, Shimiao Chen, Xiangyang Xu, Ting Jin, Qile Xu, Zongxiu Xu, Demin Zhou, Xufei Zhu, Chengming Guang, Shouhong Feng, Xuezhu Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title | Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title_full | Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title_fullStr | Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title_full_unstemmed | Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title_short | Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
title_sort | antisense ribosomal sirnas inhibit rna polymerase i-directed transcription in c. elegans |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450093/ https://www.ncbi.nlm.nih.gov/pubmed/34365510 http://dx.doi.org/10.1093/nar/gkab662 |
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