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Role for the related poly(ADP-Ribose) polymerases tankyrase 1 and 2 at human telomeres.相关的聚(ADP - 核糖)聚合酶端粒酶1和2在人类端粒中的作用。
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TIN2 is a tankyrase 1 PARP modulator in the TRF1 telomere length control complex.TIN2是端粒重复结合因子1(TRF1)端粒长度控制复合体中的一种端锚聚合酶1聚(ADP-核糖)聚合酶调节剂。
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Generation and characterization of telomere length maintenance in tankyrase 2-deficient mice.端粒酶2缺陷小鼠中端粒长度维持的产生与表征
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Tankyrase, a poly(ADP-ribose) polymerase at human telomeres.端粒酶,一种存在于人类端粒的聚(ADP-核糖)聚合酶。
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本文引用的文献

1
Tankyrase-1 polymerization of poly(ADP-ribose) is required for spindle structure and function.端锚聚合酶-1对聚(ADP-核糖)的聚合作用是纺锤体结构和功能所必需的。
Nat Cell Biol. 2005 Nov;7(11):1133-9. doi: 10.1038/ncb1322.
2
Shelterin: the protein complex that shapes and safeguards human telomeres.端粒保护蛋白复合体:塑造并保护人类端粒的蛋白质复合体。
Genes Dev. 2005 Sep 15;19(18):2100-10. doi: 10.1101/gad.1346005.
3
Poly(ADP-ribosyl)ation by PARP-1: 'PAR-laying' NAD+ into a nuclear signal.PARP-1介导的聚(ADP-核糖)基化:将NAD⁺“铺就”为一种核信号。
Genes Dev. 2005 Sep 1;19(17):1951-67. doi: 10.1101/gad.1331805.
4
NuMA is a major acceptor of poly(ADP-ribosyl)ation by tankyrase 1 in mitosis.核有丝分裂器蛋白(NuMA)是有丝分裂过程中端锚聚合酶1进行聚(ADP-核糖基)化修饰的主要受体。
Biochem J. 2005 Oct 15;391(Pt 2):177-84. doi: 10.1042/BJ20050885.
5
An increase in telomere sister chromatid exchange in murine embryonic stem cells possessing critically shortened telomeres.端粒严重缩短的小鼠胚胎干细胞中端粒姐妹染色单体交换增加。
Proc Natl Acad Sci U S A. 2005 Jul 19;102(29):10256-60. doi: 10.1073/pnas.0504635102. Epub 2005 Jul 6.
6
Grb10 and Grb14: enigmatic regulators of insulin action--and more?Grb10和Grb14:胰岛素作用的神秘调节因子——还有更多作用?
Biochem J. 2005 Jun 1;388(Pt 2):393-406. doi: 10.1042/BJ20050216.
7
Tankyrase polymerization is controlled by its sterile alpha motif and poly(ADP-ribose) polymerase domains.端锚聚合酶的聚合作用由其无活性α基序和聚(ADP-核糖)聚合酶结构域控制。
Mol Cell Biol. 2004 Nov;24(22):9802-12. doi: 10.1128/MCB.24.22.9802-9812.2004.
8
The PARP superfamily.聚(ADP - 核糖)聚合酶超家族
Bioessays. 2004 Aug;26(8):882-93. doi: 10.1002/bies.20085.
9
Regulation of telomerase by telomeric proteins.端粒蛋白对端粒酶的调控。
Annu Rev Biochem. 2004;73:177-208. doi: 10.1146/annurev.biochem.73.071403.160049.
10
Role of the insulin-regulated aminopeptidase IRAP in insulin action and diabetes.胰岛素调节氨肽酶IRAP在胰岛素作用及糖尿病中的作用
Biol Pharm Bull. 2004 Jun;27(6):761-4. doi: 10.1248/bpb.27.761.

端粒酶2聚(ADP - 核糖)聚合酶结构域缺失的小鼠表现出生长缺陷,但端粒长度和封端正常。

Tankyrase 2 poly(ADP-ribose) polymerase domain-deleted mice exhibit growth defects but have normal telomere length and capping.

作者信息

Hsiao Susan J, Poitras Marc F, Cook Brandoch D, Liu Yie, Smith Susan

机构信息

Skirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Avenue, 2nd Floor, New York, NY 10016, USA.

出版信息

Mol Cell Biol. 2006 Mar;26(6):2044-54. doi: 10.1128/MCB.26.6.2044-2054.2006.

DOI:10.1128/MCB.26.6.2044-2054.2006
PMID:16507985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1430302/
Abstract

Regulation of telomere length maintenance and capping are a critical cell functions in both normal and tumor cells. Tankyrase 2 (Tnks2) is a poly(ADP-ribose) polymerase (PARP) that has been shown to modify itself and TRF1, a telomere-binding protein. We show here by overexpression studies that tankyrase 2, like its closely related homolog tankyrase 1, can function as a positive regulator of telomere length in human cells, dependent on its catalytic PARP activity. To study the role of Tnks2 in vivo, we generated mice with the Tnks2 PARP domain deleted. These mice are viable and fertile but display a growth retardation phenotype. Telomere analysis by quantitative fluorescence in situ hybridization (FISH), flow-FISH, and restriction fragment analysis showed no change in telomere length or telomere capping in these mice. To determine the requirement for Tnks2 in long-term maintenance of telomeres, we generated embryonic stem cells with the Tnks2 PARP domain deleted and observed no change, even upon prolonged growth, in telomere length or telomere capping. Together, these results suggest that Tnks2 has a role in normal growth and development but is not essential for telomere length maintenance or telomere capping in mice.

摘要

端粒长度维持和封端的调控是正常细胞和肿瘤细胞中的关键细胞功能。端锚聚合酶2(Tnks2)是一种聚(ADP-核糖)聚合酶(PARP),已被证明可对自身及端粒结合蛋白TRF1进行修饰。我们通过过表达研究表明,端锚聚合酶2与其密切相关的同源物端锚聚合酶1一样,可作为人类细胞中端粒长度的正向调节因子,这依赖于其催化性PARP活性。为了研究Tnks2在体内的作用,我们构建了缺失Tnks2 PARP结构域的小鼠。这些小鼠可存活且可育,但表现出生长迟缓的表型。通过定量荧光原位杂交(FISH)、流式FISH和限制性片段分析进行的端粒分析表明,这些小鼠的端粒长度或端粒封端没有变化。为了确定Tnks2在端粒长期维持中的需求,我们构建了缺失Tnks2 PARP结构域的胚胎干细胞,并且观察到即使在长期生长后,端粒长度或端粒封端也没有变化。总之,这些结果表明,Tnks2在正常生长和发育中起作用,但对小鼠的端粒长度维持或端粒封端并非必不可少。