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Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights

Dietary sulfur amino acid restriction, also referred to as methionine restriction, increases food intake and energy expenditure and alters body composition in rodents, resulting in improved metabolic health and a longer lifespan. Among the known nutrient-responsive signaling pathways, the evolutiona...

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Autores principales: Jonsson, William O., Margolies, Nicholas S., Anthony, Tracy G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627990/
https://www.ncbi.nlm.nih.gov/pubmed/31208042
http://dx.doi.org/10.3390/nu11061349
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author Jonsson, William O.
Margolies, Nicholas S.
Anthony, Tracy G.
author_facet Jonsson, William O.
Margolies, Nicholas S.
Anthony, Tracy G.
author_sort Jonsson, William O.
collection PubMed
description Dietary sulfur amino acid restriction, also referred to as methionine restriction, increases food intake and energy expenditure and alters body composition in rodents, resulting in improved metabolic health and a longer lifespan. Among the known nutrient-responsive signaling pathways, the evolutionary conserved integrated stress response (ISR) is a lesser-understood candidate in mediating the hormetic effects of dietary sulfur amino acid restriction (SAAR). A key feature of the ISR is the concept that a family of protein kinases phosphorylates eukaryotic initiation factor 2 (eIF2), dampening general protein synthesis to conserve cellular resources. This slowed translation simultaneously allows for preferential translation of genes with special sequence features in the 5′ leader. Among this class of mRNAs is activating transcription factor 4 (ATF4), an orchestrator of transcriptional control during nutrient stress. Several ATF4 gene targets help execute key processes affected by SAAR such as lipid metabolism, the transsulfuration pathway, and antioxidant defenses. Exploration of the canonical ISR demonstrates that eIF2 phosphorylation is not necessary for ATF4-driven changes in the transcriptome during SAAR. Additional research is needed to clarify the regulation of ATF4 and its gene targets during SAAR.
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spelling pubmed-66279902019-07-23 Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights Jonsson, William O. Margolies, Nicholas S. Anthony, Tracy G. Nutrients Review Dietary sulfur amino acid restriction, also referred to as methionine restriction, increases food intake and energy expenditure and alters body composition in rodents, resulting in improved metabolic health and a longer lifespan. Among the known nutrient-responsive signaling pathways, the evolutionary conserved integrated stress response (ISR) is a lesser-understood candidate in mediating the hormetic effects of dietary sulfur amino acid restriction (SAAR). A key feature of the ISR is the concept that a family of protein kinases phosphorylates eukaryotic initiation factor 2 (eIF2), dampening general protein synthesis to conserve cellular resources. This slowed translation simultaneously allows for preferential translation of genes with special sequence features in the 5′ leader. Among this class of mRNAs is activating transcription factor 4 (ATF4), an orchestrator of transcriptional control during nutrient stress. Several ATF4 gene targets help execute key processes affected by SAAR such as lipid metabolism, the transsulfuration pathway, and antioxidant defenses. Exploration of the canonical ISR demonstrates that eIF2 phosphorylation is not necessary for ATF4-driven changes in the transcriptome during SAAR. Additional research is needed to clarify the regulation of ATF4 and its gene targets during SAAR. MDPI 2019-06-15 /pmc/articles/PMC6627990/ /pubmed/31208042 http://dx.doi.org/10.3390/nu11061349 Text en © 2019 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 Review
Jonsson, William O.
Margolies, Nicholas S.
Anthony, Tracy G.
Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title_full Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title_fullStr Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title_full_unstemmed Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title_short Dietary Sulfur Amino Acid Restriction and the Integrated Stress Response: Mechanistic Insights
title_sort dietary sulfur amino acid restriction and the integrated stress response: mechanistic insights
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627990/
https://www.ncbi.nlm.nih.gov/pubmed/31208042
http://dx.doi.org/10.3390/nu11061349
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