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High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1

Short Interspersed Nuclear Elements (SINEs) are non-autonomous retrotransposons that comprise a large fraction of the human genome. SINEs are demethylated in human disease, but whether SINEs become transcriptionally induced and how the resulting transcripts may affect the expression of protein codin...

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Autores principales: Peterson, Maureen, Chandler, Vicki L., Bosco, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899967/
https://www.ncbi.nlm.nih.gov/pubmed/24705161
http://dx.doi.org/10.3390/genes4020226
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author Peterson, Maureen
Chandler, Vicki L.
Bosco, Giovanni
author_facet Peterson, Maureen
Chandler, Vicki L.
Bosco, Giovanni
author_sort Peterson, Maureen
collection PubMed
description Short Interspersed Nuclear Elements (SINEs) are non-autonomous retrotransposons that comprise a large fraction of the human genome. SINEs are demethylated in human disease, but whether SINEs become transcriptionally induced and how the resulting transcripts may affect the expression of protein coding genes is unknown. Here, we show that downregulation of the mRNA of the tumor suppressor gene BRCA1 is associated with increased transcription of SINEs and production of sense and antisense SINE small RNAs. We find that BRCA1 mRNA is post-transcriptionally down-regulated in a Dicer and Drosha dependent manner and that expression of a SINE inverted repeat with sequence identity to a BRCA1 intron is sufficient for downregulation of BRCA1 mRNA. These observations suggest that transcriptional activation of SINEs could contribute to a novel mechanism of RNA mediated post-transcriptional silencing of human genes.
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spelling pubmed-38999672014-03-26 High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1 Peterson, Maureen Chandler, Vicki L. Bosco, Giovanni Genes (Basel) Article Short Interspersed Nuclear Elements (SINEs) are non-autonomous retrotransposons that comprise a large fraction of the human genome. SINEs are demethylated in human disease, but whether SINEs become transcriptionally induced and how the resulting transcripts may affect the expression of protein coding genes is unknown. Here, we show that downregulation of the mRNA of the tumor suppressor gene BRCA1 is associated with increased transcription of SINEs and production of sense and antisense SINE small RNAs. We find that BRCA1 mRNA is post-transcriptionally down-regulated in a Dicer and Drosha dependent manner and that expression of a SINE inverted repeat with sequence identity to a BRCA1 intron is sufficient for downregulation of BRCA1 mRNA. These observations suggest that transcriptional activation of SINEs could contribute to a novel mechanism of RNA mediated post-transcriptional silencing of human genes. MDPI 2013-04-29 /pmc/articles/PMC3899967/ /pubmed/24705161 http://dx.doi.org/10.3390/genes4020226 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Peterson, Maureen
Chandler, Vicki L.
Bosco, Giovanni
High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title_full High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title_fullStr High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title_full_unstemmed High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title_short High SINE RNA Expression Correlates with Post-Transcriptional Downregulation of BRCA1
title_sort high sine rna expression correlates with post-transcriptional downregulation of brca1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899967/
https://www.ncbi.nlm.nih.gov/pubmed/24705161
http://dx.doi.org/10.3390/genes4020226
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