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端粒与端粒酶生物学的小鼠模型。

Mouse models for telomere and telomerase biology.

作者信息

Cheong Cheolho, Hong Kyung Uk, Lee Han-Woong

机构信息

Samsung Biomedical Research Institute, Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon 440-746, Korea.

出版信息

Exp Mol Med. 2003 Jun 30;35(3):141-53. doi: 10.1038/emm.2003.20.

DOI:10.1038/emm.2003.20
PMID:12858012
Abstract

Telomeres serve a critical role in maintenance of genomic stability in all eukaryotes, from yeast to human. The maintenance of telomeres is achieved by the telomerase complex, which is largely composed of telomerase reverse transcriptase (TERT) and telomerase RNA component (TERC). A variety of mouse models have provided valuable insights into the relationship between the telomerase complex and telomere dysfunction at the organismal level and helped understand their biological significance in human. Recently, in addition to its role in maintenance of the telomeres, novel functions of the telomerase complex have been emerging. In this review, studies of all gene-targeted or transgenic mouse models so far generated for telomerase and telomere biology are comprehensively described, and potential novel functions of telomerase are briefly discussed.

摘要

端粒在从酵母到人类的所有真核生物的基因组稳定性维持中发挥着关键作用。端粒的维持是通过端粒酶复合物实现的,该复合物主要由端粒酶逆转录酶(TERT)和端粒酶RNA组分(TERC)组成。多种小鼠模型为在生物体水平上端粒酶复合物与端粒功能障碍之间的关系提供了有价值的见解,并有助于理解它们在人类中的生物学意义。最近,除了其在维持端粒方面的作用外,端粒酶复合物的新功能也不断涌现。在这篇综述中,全面描述了迄今为止针对端粒酶和端粒生物学构建的所有基因靶向或转基因小鼠模型的研究,并简要讨论了端粒酶潜在的新功能。

相似文献

1
Mouse models for telomere and telomerase biology.端粒与端粒酶生物学的小鼠模型。
Exp Mol Med. 2003 Jun 30;35(3):141-53. doi: 10.1038/emm.2003.20.
2
Mammalian telomeres and telomerase: why they matter for cancer and aging.哺乳动物的端粒与端粒酶:它们为何对癌症和衰老至关重要。
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4
Severe growth defect in mouse cells lacking the telomerase RNA component.缺乏端粒酶RNA组分的小鼠细胞中存在严重的生长缺陷。
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The structure and function of telomerase reverse transcriptase.端粒酶逆转录酶的结构与功能。
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Expression of telomerase RNA template, but not telomerase reverse transcriptase, is limiting for telomere length maintenance in vivo.端粒酶RNA模板的表达而非端粒酶逆转录酶的表达,在体内对端粒长度维持具有限制作用。
Mol Cell Biol. 2004 Aug;24(16):7024-31. doi: 10.1128/MCB.24.16.7024-7031.2004.
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Dysfunctional telomeres promote genomic instability and metastasis in the absence of telomerase activity in oncogene induced mammary cancer.在致癌基因诱导的乳腺癌中,功能失调的端粒会在缺乏端粒酶活性的情况下促进基因组不稳定和转移。
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Telomerase inhibition in a mouse cell line with long telomeres leads to rapid telomerase reactivation.在具有长端粒的小鼠细胞系中抑制端粒酶会导致端粒酶迅速重新激活。
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4
Reflections on telomere dynamics and ageing-related diseases in humans.端粒动力学与人类衰老相关疾病的思考。
Philos Trans R Soc Lond B Biol Sci. 2018 Mar 5;373(1741). doi: 10.1098/rstb.2016.0436.
5
Expression of functional alternative telomerase RNA component gene in mouse brain and in motor neurons cells protects from oxidative stress.功能性替代端粒酶RNA组分基因在小鼠大脑和运动神经元细胞中的表达可抵御氧化应激。
Oncotarget. 2016 Nov 29;7(48):78297-78309. doi: 10.18632/oncotarget.13049.
6
A common variant in the telomerase RNA component is associated with short telomere length.端粒酶 RNA 成分中的常见变异与端粒长度较短有关。
PLoS One. 2010 Sep 27;5(9):e13048. doi: 10.1371/journal.pone.0013048.
7
No attenuation of the ATM-dependent DNA damage response in murine telomerase-deficient cells.在小鼠端粒酶缺陷细胞中,ATM 依赖性 DNA 损伤反应无衰减。
DNA Repair (Amst). 2009 Mar 1;8(3):347-53. doi: 10.1016/j.dnarep.2008.11.009. Epub 2008 Dec 25.