• 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

长寿的加利福尼亚红海胆神经系统中独特的与年龄相关的转录特征。

Unique age-related transcriptional signature in the nervous system of the long-lived red sea urchin Mesocentrotus franciscanus.

机构信息

Gloucester Marine Genomics Institute, 417 Main Street, Gloucester, MA, 01930, USA.

Department of Marine Biology and Ecology, Rosenstiel School of Marine and Atmospheric Science, University of Miami, 4600 Rickenbacker Causeway, Miami, FL, 33149, United States.

出版信息

Sci Rep. 2020 Jun 8;10(1):9182. doi: 10.1038/s41598-020-66052-3.

DOI:10.1038/s41598-020-66052-3
PMID:32514014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7280269/
Abstract

The red sea urchin, Mesocentrotus franciscanus, is one the earth's longest-lived animals, reported to live more than 100 years with indeterminate growth, life-long reproduction and no increase in mortality rate with age. To gain insight into mechanisms associated with longevity and negligible senescence, age-related transcriptional profiles were examined in tissues of the red sea urchin. Genome-wide transcriptional profiling using RNA-Seq revealed few age-related changes in gene expression in muscle and esophagus tissue. In contrast, radial nerve showed an unexpected level of complexity with the expression of 3,370 genes significantly altered more than two-fold with age, including genes involved in nerve function, signaling, metabolism, transcriptional regulation and chromatin modification. There was an age-related upregulation in expression of genes involved in synaptogenesis, axonogenesis and neuroprotection suggesting preservation of neuronal processes with age. There was also an upregulation in expression of positive regulators and key components of the AMPK pathway, autophagy, proteasome function, and the unfolded protein response. This unique age-related gene expression profile in the red sea urchin nervous system may play a role in mitigating the detrimental effects of aging in this long-lived animal.

摘要

红色海胆,Mesocentrotus franciscanus,是地球上寿命最长的动物之一,据报道寿命超过 100 年,具有不定生长、终生繁殖和死亡率随年龄增长而不增加的特点。为了深入了解与长寿和极轻微衰老相关的机制,我们研究了红色海胆组织中与年龄相关的转录谱。使用 RNA-Seq 的全基因组转录谱分析表明,肌肉和食管组织中的基因表达与年龄相关的变化很少。相比之下,放射状神经表现出出人意料的复杂性,有 3370 个基因的表达随年龄变化超过两倍,包括涉及神经功能、信号转导、代谢、转录调节和染色质修饰的基因。与突触发生、轴突发生和神经保护相关的基因表达上调,表明神经元过程随年龄的增长而得到保护。此外,AMPK 途径、自噬、蛋白酶体功能和未折叠蛋白反应的正向调节剂和关键组成部分的表达也上调。这种红色海胆神经系统中独特的与年龄相关的基因表达谱可能在减轻这种长寿动物衰老的不利影响方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/f977a2dd71a8/41598_2020_66052_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/dbfeccc27028/41598_2020_66052_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/8b591d223d4c/41598_2020_66052_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/575a0a5a2fea/41598_2020_66052_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/8730fad1f807/41598_2020_66052_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/a351f5c549d6/41598_2020_66052_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/f977a2dd71a8/41598_2020_66052_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/dbfeccc27028/41598_2020_66052_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/8b591d223d4c/41598_2020_66052_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/575a0a5a2fea/41598_2020_66052_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/8730fad1f807/41598_2020_66052_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/a351f5c549d6/41598_2020_66052_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/7280269/f977a2dd71a8/41598_2020_66052_Fig6_HTML.jpg

相似文献

1
Unique age-related transcriptional signature in the nervous system of the long-lived red sea urchin Mesocentrotus franciscanus.长寿的加利福尼亚红海胆神经系统中独特的与年龄相关的转录特征。
Sci Rep. 2020 Jun 8;10(1):9182. doi: 10.1038/s41598-020-66052-3.
2
Genomic signatures of exceptional longevity and negligible aging in the long-lived red sea urchin.长寿红海胆基因组特征:超长寿命,衰老极慢。
Cell Rep. 2024 Apr 23;43(4):114021. doi: 10.1016/j.celrep.2024.114021. Epub 2024 Apr 1.
3
Senescence and Longevity of Sea Urchins.海胆的衰老与长寿
Genes (Basel). 2020 May 20;11(5):573. doi: 10.3390/genes11050573.
4
Oxidative damage and cellular defense mechanisms in sea urchin models of aging.衰老海胆模型中的氧化损伤和细胞防御机制。
Free Radic Biol Med. 2013 Oct;63:254-63. doi: 10.1016/j.freeradbiomed.2013.05.023. Epub 2013 May 23.
5
Transcriptional profiles of early stage red sea urchins (Mesocentrotus franciscanus) reveal differential regulation of gene expression across development.早期红海胆(加州紫海胆)的转录谱揭示了整个发育过程中基因表达的差异调控。
Mar Genomics. 2019 Dec;48:100692. doi: 10.1016/j.margen.2019.05.007. Epub 2019 Jun 19.
6
Maintenance of somatic tissue regeneration with age in short- and long-lived species of sea urchins.短寿命和长寿命海胆物种随着年龄增长对体细胞组织再生的维持。
Aging Cell. 2016 Aug;15(4):778-87. doi: 10.1111/acel.12487. Epub 2016 Apr 20.
7
Age-related changes in gene expression in tissues of the sea urchin Strongylocentrotus purpuratus.与年龄相关的海胆(Strongylocentrotus purpuratus)组织中基因表达的变化。
Mech Ageing Dev. 2012 May;133(5):338-47. doi: 10.1016/j.mad.2012.03.012. Epub 2012 Mar 28.
8
Proteomic profiles reveal age-related changes in coelomic fluid of sea urchin species with different life spans.蛋白质组学谱揭示了具有不同寿命的海胆物种的体腔液中与年龄相关的变化。
Exp Gerontol. 2013 May;48(5):525-30. doi: 10.1016/j.exger.2013.01.014. Epub 2013 Feb 8.
9
Mitochondrial genome architecture of the giant red sea urchin Mesocentrotus franciscanus (Strongylocentrotidae, Echinoida).巨红海胆(Mesocentrotus franciscanus,球海胆科,海胆纲)的线粒体基因组结构
Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(1):591-2. doi: 10.3109/19401736.2014.908359. Epub 2014 Apr 14.
10
Lack of age-associated telomere shortening in long- and short-lived species of sea urchins.长寿命和短寿命海胆物种中缺乏与年龄相关的端粒缩短现象。
FEBS Lett. 2006 Aug 21;580(19):4713-7. doi: 10.1016/j.febslet.2006.07.049. Epub 2006 Jul 24.

引用本文的文献

1
Integrated m6A RNA methylation and transcriptomic analysis of Apostichopus japonicus under combined high-temperature and hypoxia stress.高温和缺氧联合胁迫下刺参的m6A RNA甲基化与转录组整合分析
BMC Genomics. 2025 Apr 10;26(1):363. doi: 10.1186/s12864-025-11532-x.
2
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy.基于广泛的多效性假设对人类长寿的多基因预测。
Sci Rep. 2024 Aug 28;14(1):19981. doi: 10.1038/s41598-024-69069-0.
3
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy.

本文引用的文献

1
Age-Related Gene Expression Signature in Rats Demonstrate Early, Late, and Linear Transcriptional Changes from Multiple Tissues.大鼠中与年龄相关的基因表达特征显示了来自多个组织的早期、晚期和线性转录变化。
Cell Rep. 2019 Sep 17;28(12):3263-3273.e3. doi: 10.1016/j.celrep.2019.08.043.
2
AMPK directly activates mTORC2 to promote cell survival during acute energetic stress.AMPK 直接激活 mTORC2 以促进急性能量应激期间的细胞存活。
Sci Signal. 2019 Jun 11;12(585):eaav3249. doi: 10.1126/scisignal.aav3249.
3
Negative senescence in sea urchins.海胆的负性衰老。
基于普遍多效性假设的人类长寿多基因预测。
medRxiv. 2023 Dec 11:2023.12.10.23299795. doi: 10.1101/2023.12.10.23299795.
4
Two distinct evolutionary conserved neural degeneration pathways characterized in a colonial chordate.在一个群体脊索动物中鉴定出两种独特的进化保守的神经退行性病变途径。
Proc Natl Acad Sci U S A. 2022 Jul 19;119(29):e2203032119. doi: 10.1073/pnas.2203032119. Epub 2022 Jul 11.
Exp Gerontol. 2019 Jul 15;122:92-98. doi: 10.1016/j.exger.2019.04.018. Epub 2019 May 4.
4
Primary cilium and brain aging: role in neural stem cells, neurodegenerative diseases and glioblastoma.初级纤毛与脑老化:在神经干细胞、神经退行性疾病和神经胶质瘤中的作用。
Ageing Res Rev. 2019 Jul;52:53-63. doi: 10.1016/j.arr.2019.04.004. Epub 2019 Apr 18.
5
Remodeling of epigenome and transcriptome landscapes with aging in mice reveals widespread induction of inflammatory responses.随着小鼠年龄的增长,表观基因组和转录组景观的重塑揭示了广泛诱导的炎症反应。
Genome Res. 2019 Apr;29(4):697-709. doi: 10.1101/gr.240093.118. Epub 2019 Mar 11.
6
Higher gene expression stability during aging in long-lived giant mole-rats than in short-lived rats.长寿的冈比亚鼹形鼠在衰老过程中的基因表达稳定性高于短命的大鼠。
Aging (Albany NY). 2018 Dec 16;10(12):3938-3956. doi: 10.18632/aging.101683.
7
mTOR/AMPK signaling in the brain: Cell metabolism, proteostasis and survival.大脑中的mTOR/AMPK信号传导:细胞代谢、蛋白质稳态与生存
Curr Opin Toxicol. 2018 Apr;8:102-110. doi: 10.1016/j.cotox.2018.05.002. Epub 2018 May 17.
8
Autophagy as a promoter of longevity: insights from model organisms.自噬作为长寿的促进因素:来自模式生物的见解。
Nat Rev Mol Cell Biol. 2018 Sep;19(9):579-593. doi: 10.1038/s41580-018-0033-y.
9
Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort.双胞胎队列中组织间基因表达均值和方差的年龄依赖性变化。
Hum Mol Genet. 2018 Feb 15;27(4):732-741. doi: 10.1093/hmg/ddx424.
10
Cellular calcium signaling in the aging brain.衰老大脑中的细胞钙信号转导。
J Chem Neuroanat. 2019 Jan;95:95-114. doi: 10.1016/j.jchemneu.2017.11.008. Epub 2017 Nov 9.