• 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

癌症发生青年研究者奖。端粒表观遗传学:哺乳动物细胞中端粒长度的高级调控。

Carcinogenesis Young Investigator Award. Telomere epigenetics: a higher-order control of telomere length in mammalian cells.

作者信息

Blasco María A

机构信息

Molecular Oncology Program, Spanish National Cancer Centre (CNIO), E-28029 Madrid, Spain.

出版信息

Carcinogenesis. 2004 Jul;25(7):1083-7. doi: 10.1093/carcin/bgh185. Epub 2004 May 6.

DOI:10.1093/carcin/bgh185
PMID:15131012
Abstract

Telomeres are capping structures at the ends of eukaryotic chromosomes composed of TTAGGG repeats bound to an array of specialized proteins. Telomeres, together with centromeres, have been classically considered heterochromatic regions. Constitutive heterochromatin domains typically consist of repetitive DNA and have a very low gene content. In addition, constitutive heterochromatin is characterized by a number of hallmark histone modifications, as well as DNA modifications. In the case of pericentric heterochromatin, several activities responsible for these epigenetic modifications have been recently identified and characterized. In contrast, very little is still known on the architecture of telomeric chromatin, as well as on the activities that may regulate its structure and function. Here, we will discuss recent findings suggesting that telomeric chromatin shares many features with pericentric chromatin, and that disruption of telomeric heterochromatin results in changes in telomere length.

摘要

端粒是真核染色体末端的帽状结构,由与一系列特殊蛋白质结合的TTAGGG重复序列组成。端粒与着丝粒一起,传统上被认为是异染色质区域。组成型异染色质结构域通常由重复DNA组成,基因含量非常低。此外,组成型异染色质的特征是有许多标志性的组蛋白修饰以及DNA修饰。就着丝粒周围异染色质而言,最近已经鉴定并表征了几种负责这些表观遗传修饰的活性。相比之下,关于端粒染色质的结构以及可能调节其结构和功能的活性,我们仍然知之甚少。在这里,我们将讨论最近的研究结果,这些结果表明端粒染色质与着丝粒周围染色质有许多共同特征,并且端粒异染色质的破坏会导致端粒长度的变化。

相似文献

1
Carcinogenesis Young Investigator Award. Telomere epigenetics: a higher-order control of telomere length in mammalian cells.癌症发生青年研究者奖。端粒表观遗传学:哺乳动物细胞中端粒长度的高级调控。
Carcinogenesis. 2004 Jul;25(7):1083-7. doi: 10.1093/carcin/bgh185. Epub 2004 May 6.
2
Telomere length regulates the epigenetic status of mammalian telomeres and subtelomeres.端粒长度调节哺乳动物端粒和亚端粒的表观遗传状态。
Nat Genet. 2007 Feb;39(2):243-50. doi: 10.1038/ng1952. Epub 2007 Jan 21.
3
Epigenetic regulation of telomere chromatin integrity in pluripotent embryonic stem cells.多能胚胎干细胞中端粒染色质完整性的表观遗传调控。
Epigenomics. 2010 Oct;2(5):639-55. doi: 10.2217/epi.10.49.
4
Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferases.Suv39h1和Suv39h2组蛋白甲基转移酶对哺乳动物细胞端粒长度的表观遗传调控。
Nat Genet. 2004 Jan;36(1):94-9. doi: 10.1038/ng1278. Epub 2003 Dec 14.
5
Budding yeast with human telomeres: a puzzling structure.带有人类端粒的出芽酵母:一种令人费解的结构。
Biochimie. 2008 Jan;90(1):108-15. doi: 10.1016/j.biochi.2007.09.009. Epub 2007 Sep 22.
6
The epigenetic regulation of mammalian telomeres.哺乳动物端粒的表观遗传调控。
Nat Rev Genet. 2007 Apr;8(4):299-309. doi: 10.1038/nrg2047.
7
Developmentally regulated transcription of mammalian telomeres by DNA-dependent RNA polymerase II.由DNA依赖性RNA聚合酶II对哺乳动物端粒进行的发育调控转录。
Nat Cell Biol. 2008 Feb;10(2):228-36. doi: 10.1038/ncb1685. Epub 2007 Dec 23.
8
Three distinct chromatin domains in telomere ends of polytene chromosomes in Drosophila melanogaster Tel mutants.果蝇Tel突变体多线染色体端粒末端的三个不同染色质结构域。
J Cell Sci. 2005 Dec 1;118(Pt 23):5465-77. doi: 10.1242/jcs.02654. Epub 2005 Nov 8.
9
Euchromatic and heterochromatic domains at Drosophila telomeres.果蝇端粒处的常染色质和异染色质结构域。
Biochem Cell Biol. 2005 Aug;83(4):477-85. doi: 10.1139/o05-053.
10
Suv4-20h deficiency results in telomere elongation and derepression of telomere recombination.Suv4-20h缺陷导致端粒延长和端粒重组的去抑制。
J Cell Biol. 2007 Sep 10;178(6):925-36. doi: 10.1083/jcb.200703081.

引用本文的文献

1
Bring It to an End: Does Telomeres Size Matter?走向尽头:端粒大小重要吗?
Cells. 2019 Jan 8;8(1):30. doi: 10.3390/cells8010030.
2
Telomere length and advanced diffusion MRI as biomarkers for repetitive mild traumatic brain injury in adolescent rats.端粒长度和高级弥散 MRI 作为青少年大鼠重复轻度创伤性脑损伤的生物标志物。
Neuroimage Clin. 2018 Jan 31;18:315-324. doi: 10.1016/j.nicl.2018.01.033. eCollection 2018.
3
Premature Physiologic Aging as a Paradigm for Understanding Increased Risk of Adverse Health Across the Lifespan of Survivors of Childhood Cancer.
过早的生理衰老可作为理解儿童癌症幸存者一生中健康风险增加的一个范例。
J Clin Oncol. 2018 Jul 20;36(21):2206-2215. doi: 10.1200/JCO.2017.76.7467. Epub 2018 Jun 6.
4
Telomere Maintenance Mechanisms in Cancer.癌症中的端粒维持机制
Genes (Basel). 2018 May 3;9(5):241. doi: 10.3390/genes9050241.
5
Intergenerational Transmission of Paternal Epigenetic Marks: Mechanisms Influencing Susceptibility to Post-Concussion Symptomology in a Rodent Model.代际传递的父系表观遗传标记:影响啮齿动物模型创伤性脑损伤后症状易感性的机制。
Sci Rep. 2017 Aug 2;7(1):7171. doi: 10.1038/s41598-017-07784-7.
6
BRCA1/2 mutations perturb telomere biology: characterization of structural and functional abnormalities in vitro and in vivo.BRCA1/2突变扰乱端粒生物学:体内外结构与功能异常的特征分析
Oncotarget. 2016 Jan 19;7(3):2433-54. doi: 10.18632/oncotarget.5693.
7
RHPS4 G-quadruplex ligand induces anti-proliferative effects in brain tumor cells.RHPS4 G-四链体配体可诱导脑肿瘤细胞的抗增殖作用。
PLoS One. 2014 Jan 15;9(1):e86187. doi: 10.1371/journal.pone.0086187. eCollection 2014.
8
Characterization and rescue of telomeric abnormalities in ICF syndrome type I fibroblasts.ICF 综合征 I 型成纤维细胞中端粒异常的特征及挽救。
Front Oncol. 2013 Feb 28;3:35. doi: 10.3389/fonc.2013.00035. eCollection 2013.
9
Reprogramming of telomeric regions during the generation of human induced pluripotent stem cells and subsequent differentiation into fibroblast-like derivatives.在人类诱导多能干细胞的生成过程中以及随后向成纤维细胞样衍生物的分化过程中,端粒区域的重编程。
Epigenetics. 2011 Jan;6(1):63-75. doi: 10.4161/epi.6.1.13390. Epub 2011 Jan 1.
10
Function, replication and structure of the mammalian telomere.哺乳动物端粒的功能、复制和结构。
Cytotechnology. 2004 Jun;45(1-2):3-12. doi: 10.1007/s10616-004-5120-6.