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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2018-02-01
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Online Access: | https://doi.org/10.1038/s41598-018-21445-3 |
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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 |
work_keys_str_mv |
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