• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

鉴定小鼠肝细胞和心肌细胞中的幼年相关基因。

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

机构信息

Molecular Neuroscience Research Center (MNRC), Shiga University of Medical Science, Tsukinowa-cho, Seta, Otsu, Shiga, 520-2192, Japan.

Department of Systems BioMedicine, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.

出版信息

Sci Rep. 2018 Feb 15;8(1):3132. doi: 10.1038/s41598-018-21445-3.

DOI:10.1038/s41598-018-21445-3
PMID:29449671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5814429/
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.

摘要

年轻人具有成年人所没有的独特特征。与成年人相比,幼年动物在生长、愈合、学习和可塑性方面表现出更高的活力。建立这些幼年特征的机制尚未完全了解。为了更好地理解上述特性的分子组成部分,我们通过高通量测序对不同年龄的小鼠细胞进行了全面的转录组分析,鉴定出在年轻细胞中选择性高表达的基因。这些基因,统称为“与年轻相关的基因”(JAGs),在选择性剪接、磷酸化和细胞外基质(ECM)等功能中表现出显著富集。这意味着细胞水平上的年轻可能是通过这些功能实现的。JAG 突变与早衰综合征和生长障碍有关。因此,JAGs 可能会组织年轻动物的年轻特性,对 JAGs 的分析可能会为治疗遗传疾病提供科学和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/ba7d03f090d9/41598_2018_21445_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/45fb4cd8b84b/41598_2018_21445_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/32ad46f0d0b2/41598_2018_21445_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/cb942947c14c/41598_2018_21445_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/a1f5d2741ced/41598_2018_21445_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/7e0470052eb6/41598_2018_21445_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/17f4eed0607b/41598_2018_21445_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/ba7d03f090d9/41598_2018_21445_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/45fb4cd8b84b/41598_2018_21445_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/32ad46f0d0b2/41598_2018_21445_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/cb942947c14c/41598_2018_21445_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/a1f5d2741ced/41598_2018_21445_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/7e0470052eb6/41598_2018_21445_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/17f4eed0607b/41598_2018_21445_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/5814429/ba7d03f090d9/41598_2018_21445_Fig7_HTML.jpg

相似文献

1
Identification of juvenility-associated genes in the mouse hepatocytes and cardiomyocytes.鉴定小鼠肝细胞和心肌细胞中的幼年相关基因。
Sci Rep. 2018 Feb 15;8(1):3132. doi: 10.1038/s41598-018-21445-3.
2
The juvenility-associated long noncoding RNA maintains cellular juvenescence.与年轻相关的长非编码 RNA 维持细胞的年轻状态。
J Cell Sci. 2019 Apr 16;132(8):jcs227801. doi: 10.1242/jcs.227801.
3
Integrative analyses of RNA editing, alternative splicing, and expression of young genes in human brain transcriptome by deep RNA sequencing.通过深度 RNA 测序对人类大脑转录组中的 RNA 编辑、可变剪接和年轻基因表达进行综合分析。
J Mol Cell Biol. 2015 Aug;7(4):314-25. doi: 10.1093/jmcb/mjv043. Epub 2015 Jul 17.
4
Transcriptome Sequencing: RNA-Seq.转录组测序:RNA测序
Methods Mol Biol. 2018;1754:15-27. doi: 10.1007/978-1-4939-7717-8_2.
5
Deep sequencing-generated modules demonstrate coherent expression patterns for various cardiac diseases.深度测序生成的模块展示了各种心脏疾病的连贯表达模式。
Gene. 2015 Dec 10;574(1):53-60. doi: 10.1016/j.gene.2015.07.080. Epub 2015 Jul 29.
6
Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.转录组测序揭示亨廷顿舞蹈病中异常的可变剪接。
Hum Mol Genet. 2016 Aug 15;25(16):3454-3466. doi: 10.1093/hmg/ddw187. Epub 2016 Jul 4.
7
AAV9-mediated Rbm24 overexpression induces fibrosis in the mouse heart.腺相关病毒 9 介导的 Rbm24 过表达诱导小鼠心脏纤维化。
Sci Rep. 2018 Aug 3;8(1):11696. doi: 10.1038/s41598-018-29552-x.
8
Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events.使用合成长读长测序的综合转录组分析揭示了远距离剪接事件的分子共关联。
Nat Biotechnol. 2015 Jul;33(7):736-42. doi: 10.1038/nbt.3242. Epub 2015 May 18.
9
Meta-Analysis of Transcriptome Regulation During Induction to Cardiac Myocyte Fate From Mouse and Human Fibroblasts.从小鼠和人成纤维细胞诱导为心肌细胞命运过程中转录组调控的荟萃分析
J Cell Physiol. 2017 Aug;232(8):2053-2062. doi: 10.1002/jcp.25580. Epub 2017 Mar 24.
10
Transcriptome analysis in cardiomyocyte-specific differentiation of murine embryonic stem cells reveals transcriptional regulation network.小鼠胚胎干细胞心肌细胞特异性分化中的转录组分析揭示了转录调控网络。
Gene Expr Patterns. 2014 Sep;16(1):8-22. doi: 10.1016/j.gep.2014.07.002. Epub 2014 Jul 21.

引用本文的文献

1
KNTC1 introduces segmental heterogeneity to mitochondria.KNTC1 给线粒体引入了片段异质性。
Dis Model Mech. 2025 Mar 1;18(3). doi: 10.1242/dmm.052063. Epub 2025 Mar 4.
2
Bex1 is essential for ciliogenesis and harbours biomolecular condensate-forming capacity.Bex1 对于纤毛发生是必需的,并且具有形成生物分子凝聚物的能力。
BMC Biol. 2022 Feb 10;20(1):42. doi: 10.1186/s12915-022-01246-x.
3
Gm14230 controls Tbc1d24 cytoophidia and neuronal cellular juvenescence.Gm14230 控制 Tbc1d24 细胞丝状伪足和神经元细胞年轻化。

本文引用的文献

1
A Simplified, Langendorff-Free Method for Concomitant Isolation of Viable Cardiac Myocytes and Nonmyocytes From the Adult Mouse Heart.一种从成年小鼠心脏中同时分离存活心肌细胞和非心肌细胞的简化的、无需Langendorff装置的方法。
Circ Res. 2016 Sep 30;119(8):909-20. doi: 10.1161/CIRCRESAHA.116.309202. Epub 2016 Aug 8.
2
Organ-Size Regulation in Mammals.哺乳动物的器官大小调控
Cold Spring Harb Perspect Biol. 2015 Jul 17;7(9):a019240. doi: 10.1101/cshperspect.a019240.
3
Exome sequencing of hepatoblastoma reveals novel mutations and cancer genes in the Wnt pathway and ubiquitin ligase complex.
PLoS One. 2021 Apr 22;16(4):e0248517. doi: 10.1371/journal.pone.0248517. eCollection 2021.
4
Alternative RNA Splicing in Fatty Liver Disease.脂肪性肝病中的可变剪接。
Front Endocrinol (Lausanne). 2021 Feb 26;12:613213. doi: 10.3389/fendo.2021.613213. eCollection 2021.
5
Neuroepithelial cell competition triggers loss of cellular juvenescence.神经上皮细胞竞争引发细胞幼态持续丧失。
Sci Rep. 2020 Oct 22;10(1):18044. doi: 10.1038/s41598-020-74874-4.
6
Srsf7 Establishes the Juvenile Transcriptome through Age-Dependent Alternative Splicing in Mice.Srsf7通过小鼠中年龄依赖性可变剪接建立幼年转录组。
iScience. 2020 Mar 27;23(3):100929. doi: 10.1016/j.isci.2020.100929. Epub 2020 Feb 22.
外显子组测序分析肝母细胞瘤揭示 Wnt 通路和泛素连接酶复合物中的新突变和癌症基因。
Hepatology. 2014 Nov;60(5):1686-96. doi: 10.1002/hep.27243. Epub 2014 Sep 19.
4
Uhrf1-dependent H3K23 ubiquitylation couples maintenance DNA methylation and replication.UHRF1 依赖性 H3K23 泛素化将维持 DNA 甲基化与复制偶联。
Nature. 2013 Oct 10;502(7470):249-53. doi: 10.1038/nature12488. Epub 2013 Sep 8.
5
Cardiomyocyte proliferation contributes to heart growth in young humans.心肌细胞增殖有助于人类幼体心脏生长。
Proc Natl Acad Sci U S A. 2013 Jan 22;110(4):1446-51. doi: 10.1073/pnas.1214608110. Epub 2013 Jan 9.
6
Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation.UHRF1 与甲基化 H3K9 结合指导 DNA 甲基化的维持。
Nat Struct Mol Biol. 2012 Nov;19(11):1155-60. doi: 10.1038/nsmb.2391. Epub 2012 Sep 30.
7
Natural restoration of critical period plasticity in the juvenile and adult primary auditory cortex.在幼年和成年初级听觉皮层中,关键期可塑性的自然恢复。
J Neurosci. 2011 Apr 13;31(15):5625-34. doi: 10.1523/JNEUROSCI.6470-10.2011.
8
Postnatal leptin is necessary for maturation of numerous organs in newborn rats.新生大鼠出生后瘦素对于许多器官的成熟是必需的。
Organogenesis. 2011 Apr-Jun;7(2):88-94. doi: 10.4161/org.7.2.14871. Epub 2011 Apr 1.
9
Dynamic instability of genomic methylation patterns in pluripotent stem cells.多能干细胞中基因组甲基化模式的动态不稳定性。
Epigenetics Chromatin. 2010 Sep 24;3(1):17. doi: 10.1186/1756-8935-3-17.
10
Energy metabolic phenotype of the cardiomyocyte during development, differentiation, and postnatal maturation.心肌细胞在发育、分化和出生后成熟过程中的能量代谢表型。
J Cardiovasc Pharmacol. 2010 Aug;56(2):130-40. doi: 10.1097/FJC.0b013e3181e74a14.