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Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon
Excessive accumulation of polyamines causes cytotoxicity, including inhibition of cell growth and a decrease in viability. We investigated the mechanism of cytotoxicity caused by spermidine accumulation under various conditions using an Escherichia coli strain deficient in spermidine acetyltransfera...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177335/ https://www.ncbi.nlm.nih.gov/pubmed/32244348 http://dx.doi.org/10.3390/ijms21072406 |
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author | Sakamoto, Akihiko Sahara, Junpei Kawai, Gota Yamamoto, Kaneyoshi Ishihama, Akira Uemura, Takeshi Igarashi, Kazuei Kashiwagi, Keiko Terui, Yusuke |
author_facet | Sakamoto, Akihiko Sahara, Junpei Kawai, Gota Yamamoto, Kaneyoshi Ishihama, Akira Uemura, Takeshi Igarashi, Kazuei Kashiwagi, Keiko Terui, Yusuke |
author_sort | Sakamoto, Akihiko |
collection | PubMed |
description | Excessive accumulation of polyamines causes cytotoxicity, including inhibition of cell growth and a decrease in viability. We investigated the mechanism of cytotoxicity caused by spermidine accumulation under various conditions using an Escherichia coli strain deficient in spermidine acetyltransferase (SAT), a key catabolic enzyme in controlling polyamine levels. Due to the excessive accumulation of polyamines by the addition of exogenous spermidine to the growth medium, cell growth and viability were markedly decreased through translational repression of specific proteins [RMF (ribosome modulation factor) and Fis (rRNA transcription factor) etc.] encoded by members of polyamine modulon, which are essential for cell growth and viability. In particular, synthesis of proteins that have unusual locations of the Shine–Dalgarno (SD) sequence in their mRNAs was inhibited. In order to elucidate the molecular mechanism of cytotoxicity by the excessive accumulation of spermidine, the spermidine-dependent structural change of the bulged-out region in the mRNA at the initiation site of the rmf mRNA was examined using NMR analysis. It was suggested that the structure of the mRNA bulged-out region is affected by excess spermidine, so the SD sequence of the rmf mRNA cannot approach initiation codon AUG. |
format | Online Article Text |
id | pubmed-7177335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71773352020-04-28 Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon Sakamoto, Akihiko Sahara, Junpei Kawai, Gota Yamamoto, Kaneyoshi Ishihama, Akira Uemura, Takeshi Igarashi, Kazuei Kashiwagi, Keiko Terui, Yusuke Int J Mol Sci Article Excessive accumulation of polyamines causes cytotoxicity, including inhibition of cell growth and a decrease in viability. We investigated the mechanism of cytotoxicity caused by spermidine accumulation under various conditions using an Escherichia coli strain deficient in spermidine acetyltransferase (SAT), a key catabolic enzyme in controlling polyamine levels. Due to the excessive accumulation of polyamines by the addition of exogenous spermidine to the growth medium, cell growth and viability were markedly decreased through translational repression of specific proteins [RMF (ribosome modulation factor) and Fis (rRNA transcription factor) etc.] encoded by members of polyamine modulon, which are essential for cell growth and viability. In particular, synthesis of proteins that have unusual locations of the Shine–Dalgarno (SD) sequence in their mRNAs was inhibited. In order to elucidate the molecular mechanism of cytotoxicity by the excessive accumulation of spermidine, the spermidine-dependent structural change of the bulged-out region in the mRNA at the initiation site of the rmf mRNA was examined using NMR analysis. It was suggested that the structure of the mRNA bulged-out region is affected by excess spermidine, so the SD sequence of the rmf mRNA cannot approach initiation codon AUG. MDPI 2020-03-31 /pmc/articles/PMC7177335/ /pubmed/32244348 http://dx.doi.org/10.3390/ijms21072406 Text en © 2020 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 Sakamoto, Akihiko Sahara, Junpei Kawai, Gota Yamamoto, Kaneyoshi Ishihama, Akira Uemura, Takeshi Igarashi, Kazuei Kashiwagi, Keiko Terui, Yusuke Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title | Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title_full | Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title_fullStr | Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title_full_unstemmed | Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title_short | Cytotoxic Mechanism of Excess Polyamines Functions through Translational Repression of Specific Proteins Encoded by Polyamine Modulon |
title_sort | cytotoxic mechanism of excess polyamines functions through translational repression of specific proteins encoded by polyamine modulon |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177335/ https://www.ncbi.nlm.nih.gov/pubmed/32244348 http://dx.doi.org/10.3390/ijms21072406 |
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