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High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels
The eri-1 gene encodes a 3′ exonuclease that can negatively regulate RNA interference via siRNase activity. High-dose siRNAs (hd-siRNAs) can enhance Eri-1 expression, which in return degrade siRNAs and greatly reduces RNAi efficiency. Here we report that hd-siRNAs induce mouse Eri-1 (meri-1) express...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198429/ https://www.ncbi.nlm.nih.gov/pubmed/22039495 http://dx.doi.org/10.1371/journal.pone.0026466 |
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author | Bian, Yingnan Zhou, Wei Zhao, Yingchun Li, Xiaoping Geng, Wei Hao, Ruixin Yang, Qing Huang, Weida |
author_facet | Bian, Yingnan Zhou, Wei Zhao, Yingchun Li, Xiaoping Geng, Wei Hao, Ruixin Yang, Qing Huang, Weida |
author_sort | Bian, Yingnan |
collection | PubMed |
description | The eri-1 gene encodes a 3′ exonuclease that can negatively regulate RNA interference via siRNase activity. High-dose siRNAs (hd-siRNAs) can enhance Eri-1 expression, which in return degrade siRNAs and greatly reduces RNAi efficiency. Here we report that hd-siRNAs induce mouse Eri-1 (meri-1) expression through the recruitment of Sp1, Ets-1, and STAT3 to the meri-1 promoter and the formation of an Sp1-Ets-1-STAT3 complex. In addition, hd-siRNAs also abolish the 3′ untranslated region (UTR) mediated posttranscriptional repression of meri-1. Our findings demonstrate the molecular mechanism underlying the upregulation of meri-1 by hd-siRNA. |
format | Online Article Text |
id | pubmed-3198429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31984292011-10-28 High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels Bian, Yingnan Zhou, Wei Zhao, Yingchun Li, Xiaoping Geng, Wei Hao, Ruixin Yang, Qing Huang, Weida PLoS One Research Article The eri-1 gene encodes a 3′ exonuclease that can negatively regulate RNA interference via siRNase activity. High-dose siRNAs (hd-siRNAs) can enhance Eri-1 expression, which in return degrade siRNAs and greatly reduces RNAi efficiency. Here we report that hd-siRNAs induce mouse Eri-1 (meri-1) expression through the recruitment of Sp1, Ets-1, and STAT3 to the meri-1 promoter and the formation of an Sp1-Ets-1-STAT3 complex. In addition, hd-siRNAs also abolish the 3′ untranslated region (UTR) mediated posttranscriptional repression of meri-1. Our findings demonstrate the molecular mechanism underlying the upregulation of meri-1 by hd-siRNA. Public Library of Science 2011-10-19 /pmc/articles/PMC3198429/ /pubmed/22039495 http://dx.doi.org/10.1371/journal.pone.0026466 Text en Bian et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bian, Yingnan Zhou, Wei Zhao, Yingchun Li, Xiaoping Geng, Wei Hao, Ruixin Yang, Qing Huang, Weida High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title | High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title_full | High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title_fullStr | High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title_full_unstemmed | High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title_short | High-Dose siRNAs Upregulate Mouse Eri-1 at both Transcription and Posttranscription Levels |
title_sort | high-dose sirnas upregulate mouse eri-1 at both transcription and posttranscription levels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198429/ https://www.ncbi.nlm.nih.gov/pubmed/22039495 http://dx.doi.org/10.1371/journal.pone.0026466 |
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