Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination

One important question in aging research is how differences in genomics and transcriptomics determine the maximum lifespan in various species. Despite recent progress, much is still unclear on the topic, partly due to the lack of samples in nonmodel organisms and due to challenges in direct comparis...

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Published in:Aging Cell
Main Authors: Toren, Dmitri, Kulaga, Anton, Jethva, Mineshbhai, Rubin, Eitan, Snezhkina, Anastasia V., Kudryavtseva, Anna V., Nowicki, Dmitry, Tacutu, Robi, Moskalev, Alexey A., Fraifeld, Vadim E.
Format: Text
Language:English
Published: John Wiley and Sons Inc. 2020
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433004/
http://www.ncbi.nlm.nih.gov/pubmed/32515539
https://doi.org/10.1111/acel.13158
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spelling ftpubmed:oai:pubmedcentral.nih.gov:7433004 2023-05-15T15:09:40+02:00 Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination Toren, Dmitri Kulaga, Anton Jethva, Mineshbhai Rubin, Eitan Snezhkina, Anastasia V. Kudryavtseva, Anna V. Nowicki, Dmitry Tacutu, Robi Moskalev, Alexey A. Fraifeld, Vadim E. 2020-06-09 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433004/ http://www.ncbi.nlm.nih.gov/pubmed/32515539 https://doi.org/10.1111/acel.13158 en eng John Wiley and Sons Inc. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433004/ http://www.ncbi.nlm.nih.gov/pubmed/32515539 http://dx.doi.org/10.1111/acel.13158 © 2020 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. CC-BY Aging Cell Original Papers Text 2020 ftpubmed https://doi.org/10.1111/acel.13158 2020-08-23T00:36:54Z One important question in aging research is how differences in genomics and transcriptomics determine the maximum lifespan in various species. Despite recent progress, much is still unclear on the topic, partly due to the lack of samples in nonmodel organisms and due to challenges in direct comparisons of transcriptomes from different species. The novel ranking‐based method that we employ here is used to analyze gene expression in the gray whale and compare its de novo assembled transcriptome with that of other long‐ and short‐lived mammals. Gray whales are among the top 1% longest‐lived mammals. Despite the extreme environment, or maybe due to a remarkable adaptation to its habitat (intermittent hypoxia, Arctic water, and high pressure), gray whales reach at least the age of 77 years. In this work, we show that long‐lived mammals share common gene expression patterns between themselves, including high expression of DNA maintenance and repair, ubiquitination, apoptosis, and immune responses. Additionally, the level of expression for gray whale orthologs of pro‐ and anti‐longevity genes found in model organisms is in support of their alleged role and direction in lifespan determination. Remarkably, among highly expressed pro‐longevity genes many are stress‐related, reflecting an adaptation to extreme environmental conditions. The conducted analysis suggests that the gray whale potentially possesses high resistance to cancer and stress, at least in part ensuring its longevity. This new transcriptome assembly also provides important resources to support the efforts of maintaining the endangered population of gray whales. Text Arctic PubMed Central (PMC) Arctic Aging Cell 19 7
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Original Papers
spellingShingle Original Papers
Toren, Dmitri
Kulaga, Anton
Jethva, Mineshbhai
Rubin, Eitan
Snezhkina, Anastasia V.
Kudryavtseva, Anna V.
Nowicki, Dmitry
Tacutu, Robi
Moskalev, Alexey A.
Fraifeld, Vadim E.
Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
topic_facet Original Papers
description One important question in aging research is how differences in genomics and transcriptomics determine the maximum lifespan in various species. Despite recent progress, much is still unclear on the topic, partly due to the lack of samples in nonmodel organisms and due to challenges in direct comparisons of transcriptomes from different species. The novel ranking‐based method that we employ here is used to analyze gene expression in the gray whale and compare its de novo assembled transcriptome with that of other long‐ and short‐lived mammals. Gray whales are among the top 1% longest‐lived mammals. Despite the extreme environment, or maybe due to a remarkable adaptation to its habitat (intermittent hypoxia, Arctic water, and high pressure), gray whales reach at least the age of 77 years. In this work, we show that long‐lived mammals share common gene expression patterns between themselves, including high expression of DNA maintenance and repair, ubiquitination, apoptosis, and immune responses. Additionally, the level of expression for gray whale orthologs of pro‐ and anti‐longevity genes found in model organisms is in support of their alleged role and direction in lifespan determination. Remarkably, among highly expressed pro‐longevity genes many are stress‐related, reflecting an adaptation to extreme environmental conditions. The conducted analysis suggests that the gray whale potentially possesses high resistance to cancer and stress, at least in part ensuring its longevity. This new transcriptome assembly also provides important resources to support the efforts of maintaining the endangered population of gray whales.
format Text
author Toren, Dmitri
Kulaga, Anton
Jethva, Mineshbhai
Rubin, Eitan
Snezhkina, Anastasia V.
Kudryavtseva, Anna V.
Nowicki, Dmitry
Tacutu, Robi
Moskalev, Alexey A.
Fraifeld, Vadim E.
author_facet Toren, Dmitri
Kulaga, Anton
Jethva, Mineshbhai
Rubin, Eitan
Snezhkina, Anastasia V.
Kudryavtseva, Anna V.
Nowicki, Dmitry
Tacutu, Robi
Moskalev, Alexey A.
Fraifeld, Vadim E.
author_sort Toren, Dmitri
title Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
title_short Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
title_full Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
title_fullStr Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
title_full_unstemmed Gray whale transcriptome reveals longevity adaptations associated with DNA repair and ubiquitination
title_sort gray whale transcriptome reveals longevity adaptations associated with dna repair and ubiquitination
publisher John Wiley and Sons Inc.
publishDate 2020
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433004/
http://www.ncbi.nlm.nih.gov/pubmed/32515539
https://doi.org/10.1111/acel.13158
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op_source Aging Cell
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433004/
http://www.ncbi.nlm.nih.gov/pubmed/32515539
http://dx.doi.org/10.1111/acel.13158
op_rights © 2020 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
op_rightsnorm CC-BY
op_doi https://doi.org/10.1111/acel.13158
container_title Aging Cell
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