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DAF-16 target identification in C. elegans: past, present and future

In C. elegans, mutations in the conserved insulin/IGF-1 signaling (IIS) pathway lead to a robust extension in lifespan, improved late life health, and protection from age-related disease. These effects are mediated by the FoxO transcription factor DAF-16 which lies downstream of the IIS kinase casca...

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Autor principal: Tullet, Jennifer M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361755/
https://www.ncbi.nlm.nih.gov/pubmed/25156270
http://dx.doi.org/10.1007/s10522-014-9527-y
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author Tullet, Jennifer M. A.
author_facet Tullet, Jennifer M. A.
author_sort Tullet, Jennifer M. A.
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description In C. elegans, mutations in the conserved insulin/IGF-1 signaling (IIS) pathway lead to a robust extension in lifespan, improved late life health, and protection from age-related disease. These effects are mediated by the FoxO transcription factor DAF-16 which lies downstream of the IIS kinase cascade. Identifying and functionally testing DAF-16 target genes has been a focal point of ageing research for the last 10 years. Here, I review the recent advances in identifying and understanding IIS/DAF-16 targets. These studies continue to reveal the intricate nature of the IIS/DAF-16 gene regulation network and are helping us to understand the mechanisms that control lifespan. Ageing and age related disease is an area of intense public interest, and the biochemical characterization of the genes involved will be critical for identifying drugs to improve the health of our ageing population.
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spelling pubmed-43617552015-03-20 DAF-16 target identification in C. elegans: past, present and future Tullet, Jennifer M. A. Biogerontology Review Article In C. elegans, mutations in the conserved insulin/IGF-1 signaling (IIS) pathway lead to a robust extension in lifespan, improved late life health, and protection from age-related disease. These effects are mediated by the FoxO transcription factor DAF-16 which lies downstream of the IIS kinase cascade. Identifying and functionally testing DAF-16 target genes has been a focal point of ageing research for the last 10 years. Here, I review the recent advances in identifying and understanding IIS/DAF-16 targets. These studies continue to reveal the intricate nature of the IIS/DAF-16 gene regulation network and are helping us to understand the mechanisms that control lifespan. Ageing and age related disease is an area of intense public interest, and the biochemical characterization of the genes involved will be critical for identifying drugs to improve the health of our ageing population. Springer Netherlands 2014-08-26 2015 /pmc/articles/PMC4361755/ /pubmed/25156270 http://dx.doi.org/10.1007/s10522-014-9527-y Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Review Article
Tullet, Jennifer M. A.
DAF-16 target identification in C. elegans: past, present and future
title DAF-16 target identification in C. elegans: past, present and future
title_full DAF-16 target identification in C. elegans: past, present and future
title_fullStr DAF-16 target identification in C. elegans: past, present and future
title_full_unstemmed DAF-16 target identification in C. elegans: past, present and future
title_short DAF-16 target identification in C. elegans: past, present and future
title_sort daf-16 target identification in c. elegans: past, present and future
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361755/
https://www.ncbi.nlm.nih.gov/pubmed/25156270
http://dx.doi.org/10.1007/s10522-014-9527-y
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