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Genetic signature of human longevity in PKC and NF‐κB signaling

Gene variants associated with longevity are also associated with protection against cognitive decline, dementia and Alzheimer's disease, suggesting that common physiologic pathways act at the interface of longevity and cognitive function. To test the hypothesis that variants in genes implicated...

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Autores principales: Ryu, Seungjin, Han, Jeehae, Norden‐Krichmar, Trina M., Zhang, Quanwei, Lee, Seunggeun, Zhang, Zhengdong, Atzmon, Gil, Niedernhofer, Laura J., Robbins, Paul D., Barzilai, Nir, Schork, Nicholas J., Suh, Yousin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282271/
https://www.ncbi.nlm.nih.gov/pubmed/34197020
http://dx.doi.org/10.1111/acel.13362
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author Ryu, Seungjin
Han, Jeehae
Norden‐Krichmar, Trina M.
Zhang, Quanwei
Lee, Seunggeun
Zhang, Zhengdong
Atzmon, Gil
Niedernhofer, Laura J.
Robbins, Paul D.
Barzilai, Nir
Schork, Nicholas J.
Suh, Yousin
author_facet Ryu, Seungjin
Han, Jeehae
Norden‐Krichmar, Trina M.
Zhang, Quanwei
Lee, Seunggeun
Zhang, Zhengdong
Atzmon, Gil
Niedernhofer, Laura J.
Robbins, Paul D.
Barzilai, Nir
Schork, Nicholas J.
Suh, Yousin
author_sort Ryu, Seungjin
collection PubMed
description Gene variants associated with longevity are also associated with protection against cognitive decline, dementia and Alzheimer's disease, suggesting that common physiologic pathways act at the interface of longevity and cognitive function. To test the hypothesis that variants in genes implicated in cognitive function may promote exceptional longevity, we performed a comprehensive 3‐stage study to identify functional longevity‐associated variants in ~700 candidate genes in up to 450 centenarians and 500 controls by target capture sequencing analysis. We found an enrichment of longevity‐associated genes in the nPKC and NF‐κB signaling pathways by gene‐based association analyses. Functional analysis of the top three gene variants (NFKBIA, CLU, PRKCH) suggests that non‐coding variants modulate the expression of cognate genes, thereby reducing signaling through the nPKC and NF‐κB. This matches genetic studies in multiple model organisms, suggesting that the evolutionary conservation of reduced PKC and NF‐κB signaling pathways in exceptional longevity may include humans.
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spelling pubmed-82822712021-07-16 Genetic signature of human longevity in PKC and NF‐κB signaling Ryu, Seungjin Han, Jeehae Norden‐Krichmar, Trina M. Zhang, Quanwei Lee, Seunggeun Zhang, Zhengdong Atzmon, Gil Niedernhofer, Laura J. Robbins, Paul D. Barzilai, Nir Schork, Nicholas J. Suh, Yousin Aging Cell Original Articles Gene variants associated with longevity are also associated with protection against cognitive decline, dementia and Alzheimer's disease, suggesting that common physiologic pathways act at the interface of longevity and cognitive function. To test the hypothesis that variants in genes implicated in cognitive function may promote exceptional longevity, we performed a comprehensive 3‐stage study to identify functional longevity‐associated variants in ~700 candidate genes in up to 450 centenarians and 500 controls by target capture sequencing analysis. We found an enrichment of longevity‐associated genes in the nPKC and NF‐κB signaling pathways by gene‐based association analyses. Functional analysis of the top three gene variants (NFKBIA, CLU, PRKCH) suggests that non‐coding variants modulate the expression of cognate genes, thereby reducing signaling through the nPKC and NF‐κB. This matches genetic studies in multiple model organisms, suggesting that the evolutionary conservation of reduced PKC and NF‐κB signaling pathways in exceptional longevity may include humans. John Wiley and Sons Inc. 2021-07-01 2021-07 /pmc/articles/PMC8282271/ /pubmed/34197020 http://dx.doi.org/10.1111/acel.13362 Text en © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ryu, Seungjin
Han, Jeehae
Norden‐Krichmar, Trina M.
Zhang, Quanwei
Lee, Seunggeun
Zhang, Zhengdong
Atzmon, Gil
Niedernhofer, Laura J.
Robbins, Paul D.
Barzilai, Nir
Schork, Nicholas J.
Suh, Yousin
Genetic signature of human longevity in PKC and NF‐κB signaling
title Genetic signature of human longevity in PKC and NF‐κB signaling
title_full Genetic signature of human longevity in PKC and NF‐κB signaling
title_fullStr Genetic signature of human longevity in PKC and NF‐κB signaling
title_full_unstemmed Genetic signature of human longevity in PKC and NF‐κB signaling
title_short Genetic signature of human longevity in PKC and NF‐κB signaling
title_sort genetic signature of human longevity in pkc and nf‐κb signaling
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282271/
https://www.ncbi.nlm.nih.gov/pubmed/34197020
http://dx.doi.org/10.1111/acel.13362
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