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Inhibition of LINE-1 Retrotransposition by Capsaicin
Long interspersed nuclear element 1 (LINE-1 or L1) is a non-long terminal repeat (LTR) retrotransposon that constitutes approximately 17% of the human genome. Since approximately 100 copies are still competent for retrotransposition to other genomic loci, dysregulated retrotransposition of L1 is con...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214084/ https://www.ncbi.nlm.nih.gov/pubmed/30347711 http://dx.doi.org/10.3390/ijms19103243 |
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author | Nishikawa, Yuki Nakayama, Ryota Obika, Shunsuke Ohsaki, Eriko Ueda, Keiji Honda, Tomoyuki |
author_facet | Nishikawa, Yuki Nakayama, Ryota Obika, Shunsuke Ohsaki, Eriko Ueda, Keiji Honda, Tomoyuki |
author_sort | Nishikawa, Yuki |
collection | PubMed |
description | Long interspersed nuclear element 1 (LINE-1 or L1) is a non-long terminal repeat (LTR) retrotransposon that constitutes approximately 17% of the human genome. Since approximately 100 copies are still competent for retrotransposition to other genomic loci, dysregulated retrotransposition of L1 is considered to be a major risk factor of endogenous mutagenesis in humans. Thus, it is important to find drugs to regulate this process. Although various chemicals are reportedly capable of affecting L1 retrotransposition, it is poorly understood whether phytochemicals modulate L1 retrotransposition. Here, we screened a library of compounds that were derived from phytochemicals for reverse transcriptase (RT) inhibition with an in vitro RT assay. We identified capsaicin as a novel RT inhibitor that also suppressed L1 retrotransposition. The inhibitory effect of capsaicin on L1 retrotransposition was mediated neither through its receptor, nor through its modulation of the L1 promoter and/or antisense promoter activity, excluding the possibility that capsaicin indirectly affected L1 retrotransposition. Collectively, capsaicin suppressed L1 retrotransposition most likely by inhibiting the RT activity of L1 ORF2p, which is the L1-encoded RT responsible for L1 retrotransposition. Given that L1-mediated mutagenesis can cause tumorigenesis, our findings suggest the potential of capsaicin for suppressing cancer development. |
format | Online Article Text |
id | pubmed-6214084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62140842018-11-14 Inhibition of LINE-1 Retrotransposition by Capsaicin Nishikawa, Yuki Nakayama, Ryota Obika, Shunsuke Ohsaki, Eriko Ueda, Keiji Honda, Tomoyuki Int J Mol Sci Article Long interspersed nuclear element 1 (LINE-1 or L1) is a non-long terminal repeat (LTR) retrotransposon that constitutes approximately 17% of the human genome. Since approximately 100 copies are still competent for retrotransposition to other genomic loci, dysregulated retrotransposition of L1 is considered to be a major risk factor of endogenous mutagenesis in humans. Thus, it is important to find drugs to regulate this process. Although various chemicals are reportedly capable of affecting L1 retrotransposition, it is poorly understood whether phytochemicals modulate L1 retrotransposition. Here, we screened a library of compounds that were derived from phytochemicals for reverse transcriptase (RT) inhibition with an in vitro RT assay. We identified capsaicin as a novel RT inhibitor that also suppressed L1 retrotransposition. The inhibitory effect of capsaicin on L1 retrotransposition was mediated neither through its receptor, nor through its modulation of the L1 promoter and/or antisense promoter activity, excluding the possibility that capsaicin indirectly affected L1 retrotransposition. Collectively, capsaicin suppressed L1 retrotransposition most likely by inhibiting the RT activity of L1 ORF2p, which is the L1-encoded RT responsible for L1 retrotransposition. Given that L1-mediated mutagenesis can cause tumorigenesis, our findings suggest the potential of capsaicin for suppressing cancer development. MDPI 2018-10-19 /pmc/articles/PMC6214084/ /pubmed/30347711 http://dx.doi.org/10.3390/ijms19103243 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nishikawa, Yuki Nakayama, Ryota Obika, Shunsuke Ohsaki, Eriko Ueda, Keiji Honda, Tomoyuki Inhibition of LINE-1 Retrotransposition by Capsaicin |
title | Inhibition of LINE-1 Retrotransposition by Capsaicin |
title_full | Inhibition of LINE-1 Retrotransposition by Capsaicin |
title_fullStr | Inhibition of LINE-1 Retrotransposition by Capsaicin |
title_full_unstemmed | Inhibition of LINE-1 Retrotransposition by Capsaicin |
title_short | Inhibition of LINE-1 Retrotransposition by Capsaicin |
title_sort | inhibition of line-1 retrotransposition by capsaicin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214084/ https://www.ncbi.nlm.nih.gov/pubmed/30347711 http://dx.doi.org/10.3390/ijms19103243 |
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