Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes

Abstract Young individuals possess distinct properties that adults do not. The juvenile animals show higher activities for growth, healing, learning and plasticity than adults. The machinery for establishing these juvenile properties is not fully understood. To better understand the molecular consti...

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Main Authors: Faidruz Azura Jam, Yosuke Kadota, Anarmaa Mendsaikhan, Ikuo Tooyama, Masaki Mori
Format: Article
Language:English
Published: Nature Publishing Group 2018-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-21445-3
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spelling doaj-d047ec3d707d4ec6a497165c3e81efe82020-12-08T05:29:23ZengNature Publishing GroupScientific Reports2045-23222018-02-018111210.1038/s41598-018-21445-3Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytesFaidruz Azura Jam0Yosuke Kadota1Anarmaa Mendsaikhan2Ikuo Tooyama3Masaki Mori4Molecular Neuroscience Research Center (MNRC), Shiga University of Medical ScienceMolecular Neuroscience Research Center (MNRC), Shiga University of Medical ScienceMolecular Neuroscience Research Center (MNRC), Shiga University of Medical ScienceMolecular Neuroscience Research Center (MNRC), Shiga University of Medical ScienceMolecular Neuroscience Research Center (MNRC), Shiga University of Medical ScienceAbstract Young individuals possess distinct properties that adults do not. The juvenile animals show higher activities for growth, healing, learning and plasticity than adults. The machinery for establishing these juvenile properties is not fully understood. To better understand the molecular constituents for the above properties, we performed a comprehensive transcriptome analysis of differently aged cells of mice by high-throughput sequencing and identified the genes selectively highly expressed in the young cells. These genes, collectively called as juvenility-associated genes (JAGs), show significant enrichments in the functions such as alternative splicing, phosphorylation and extracellular matrix (ECM). This implies the juvenescence might be achieved by these functions at the cell level. The JAG mutations are associated with progeria syndromes and growth disorders. Thus, the JAGs might organize the juvenile property of young animals and analysis of JAGs may provide scientific and therapeutic approaches toward treating the genetic diseases.https://doi.org/10.1038/s41598-018-21445-3
collection DOAJ
language English
format Article
sources DOAJ
author Faidruz Azura Jam
Yosuke Kadota
Anarmaa Mendsaikhan
Ikuo Tooyama
Masaki Mori
spellingShingle Faidruz Azura Jam
Yosuke Kadota
Anarmaa Mendsaikhan
Ikuo Tooyama
Masaki Mori
Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
Scientific Reports
author_facet Faidruz Azura Jam
Yosuke Kadota
Anarmaa Mendsaikhan
Ikuo Tooyama
Masaki Mori
author_sort Faidruz Azura Jam
title Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
title_short Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
title_full Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
title_fullStr Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
title_full_unstemmed Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
title_sort identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-02-01
description Abstract Young individuals possess distinct properties that adults do not. The juvenile animals show higher activities for growth, healing, learning and plasticity than adults. The machinery for establishing these juvenile properties is not fully understood. To better understand the molecular constituents for the above properties, we performed a comprehensive transcriptome analysis of differently aged cells of mice by high-throughput sequencing and identified the genes selectively highly expressed in the young cells. These genes, collectively called as juvenility-associated genes (JAGs), show significant enrichments in the functions such as alternative splicing, phosphorylation and extracellular matrix (ECM). This implies the juvenescence might be achieved by these functions at the cell level. The JAG mutations are associated with progeria syndromes and growth disorders. Thus, the JAGs might organize the juvenile property of young animals and analysis of JAGs may provide scientific and therapeutic approaches toward treating the genetic diseases.
url https://doi.org/10.1038/s41598-018-21445-3
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AT ikuotooyama identificationofjuvenilityassociatedgenesinthemousehepatocytesandcardiomyocytes
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