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ATM and ATR make distinct contributions to chromosome end protection and the maintenance of telomeric DNA in Arabidopsis.在拟南芥中,ATM和ATR对染色体末端保护以及端粒DNA的维持发挥着不同作用。
Genes Dev. 2005 Sep 15;19(18):2111-5. doi: 10.1101/gad.1333805.
2
Arabidopsis ATM and ATR kinases prevent propagation of genome damage caused by telomere dysfunction.拟南芥 ATM 和 ATR 激酶可防止端粒功能障碍引起的基因组损伤的传播。
Plant Cell. 2011 Dec;23(12):4254-65. doi: 10.1105/tpc.111.092387. Epub 2011 Dec 9.
3
ATR cooperates with CTC1 and STN1 to maintain telomeres and genome integrity in Arabidopsis.ATR 通过与 CTC1 和 STN1 合作维持拟南芥端粒和基因组完整性。
Mol Biol Cell. 2012 Apr;23(8):1558-68. doi: 10.1091/mbc.E11-12-1002. Epub 2012 Feb 22.
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Protection of telomeres through independent control of ATM and ATR by TRF2 and POT1.TRF2和POT1通过对ATM和ATR的独立调控来保护端粒。
Nature. 2007 Aug 30;448(7157):1068-71. doi: 10.1038/nature06065. Epub 2007 Aug 8.
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The Arabidopsis Pot1 and Pot2 proteins function in telomere length homeostasis and chromosome end protection.拟南芥中的Pot1和Pot2蛋白在端粒长度稳态维持和染色体末端保护中发挥作用。
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Ku is required for telomeric C-rich strand maintenance but not for end-to-end chromosome fusions in Arabidopsis.拟南芥中,端粒富含C链的维持需要Ku,但染色体端对端融合则不需要。
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ATM regulates the length of individual telomere tracts in Arabidopsis.ATM调节拟南芥中单个端粒序列的长度。
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ATR and ATM play both distinct and additive roles in response to ionizing radiation.ATR和ATM在对电离辐射的反应中发挥着不同且互补的作用。
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Ataxia telangiectasia mutated (Atm) is not required for telomerase-mediated elongation of short telomeres.端粒酶介导的短端粒延长不需要共济失调毛细血管扩张症突变基因(Atm)。
Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2249-51. doi: 10.1073/pnas.0511143103. Epub 2006 Feb 7.
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Both ATM and ATR promote the efficient and accurate processing of programmed meiotic double-strand breaks.ATM和ATR都能促进程序性减数分裂双链断裂的高效准确处理。
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G2/M-checkpoint activation in fasciata1 rescues an aberrant S-phase checkpoint but causes genome instability.筋膜蛋白 1 中的 G2/M 检查点激活挽救了异常的 S 期检查点,但导致了基因组不稳定。
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Functional Diversification of Replication Protein A Paralogs and Telomere Length Maintenance in Arabidopsis.复制蛋白 A 同工基因的功能多样化与拟南芥端粒长度的维持。
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High atomic weight, high-energy radiation (HZE) induces transcriptional responses shared with conventional stresses in addition to a core "DSB" response specific to clastogenic treatments.高原子重量、高能量辐射(HZE)除了诱导与传统应激共享的转录反应外,还诱导与断裂剂治疗特异性相关的核心“DSB”反应。
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Microbial pathogens trigger host DNA double-strand breaks whose abundance is reduced by plant defense responses.微生物病原体引发宿主DNA双链断裂,而植物防御反应会降低这种双链断裂的丰度。
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9
Analysis of poly(ADP-Ribose) polymerases in Arabidopsis telomere biology.拟南芥端粒生物学中聚(ADP - 核糖)聚合酶的分析
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10
A hypomorphic mutation reveals a stringent requirement for the ATM checkpoint protein in telomere protection during early cell division in Drosophila.一个低等位基因突变揭示了 ATM 检查点蛋白在果蝇早期细胞分裂中端粒保护中的严格需求。
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本文引用的文献

1
ATM activation by DNA double-strand breaks through the Mre11-Rad50-Nbs1 complex.DNA双链断裂通过Mre11-Rad50-Nbs1复合物激活ATM。
Science. 2005 Apr 22;308(5721):551-4. doi: 10.1126/science.1108297. Epub 2005 Mar 24.
2
Late S phase-specific recruitment of Mre11 complex triggers hierarchical assembly of telomere replication proteins in Saccharomyces cerevisiae.Mre11复合物在S期晚期的特异性募集触发酿酒酵母端粒复制蛋白的分级组装。
Mol Cell. 2005 Feb 18;17(4):573-83. doi: 10.1016/j.molcel.2005.01.014.
3
The telomeric protein TRF2 binds the ATM kinase and can inhibit the ATM-dependent DNA damage response.端粒蛋白TRF2与ATM激酶结合,并能抑制ATM依赖的DNA损伤反应。
PLoS Biol. 2004 Aug;2(8):E240. doi: 10.1371/journal.pbio.0020240. Epub 2004 Aug 17.
4
Functional links between telomeres and proteins of the DNA-damage response.端粒与DNA损伤反应蛋白之间的功能联系。
Genes Dev. 2004 Aug 1;18(15):1781-99. doi: 10.1101/gad.1214504.
5
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.
6
Reciprocal association of the budding yeast ATM-related proteins Tel1 and Mec1 with telomeres in vivo.芽殖酵母中与ATM相关的蛋白质Tel1和Mec1在体内与端粒的相互关联。
Mol Cell. 2004 May 21;14(4):515-22. doi: 10.1016/s1097-2765(04)00262-x.
7
Molecular analysis of telomere fusions in Arabidopsis: multiple pathways for chromosome end-joining.拟南芥中端粒融合的分子分析:染色体末端连接的多种途径
EMBO J. 2004 Jun 2;23(11):2304-13. doi: 10.1038/sj.emboj.7600236. Epub 2004 May 13.
8
ATR regulates a G2-phase cell-cycle checkpoint in Arabidopsis thaliana.ATR调节拟南芥中的G2期细胞周期检查点。
Plant Cell. 2004 May;16(5):1091-104. doi: 10.1105/tpc.018903. Epub 2004 Apr 9.
9
RPA regulates telomerase action by providing Est1p access to chromosome ends.RPA通过使Est1p接近染色体末端来调节端粒酶的作用。
Nat Genet. 2004 Jan;36(1):46-54. doi: 10.1038/ng1284. Epub 2003 Dec 21.
10
Short telomeres and ataxia-telangiectasia mutated deficiency cooperatively increase telomere dysfunction and suppress tumorigenesis.短端粒与共济失调毛细血管扩张症突变缺陷协同增加端粒功能障碍并抑制肿瘤发生。
Cancer Res. 2003 Dec 1;63(23):8188-96.

在拟南芥中,ATM和ATR对染色体末端保护以及端粒DNA的维持发挥着不同作用。

ATM and ATR make distinct contributions to chromosome end protection and the maintenance of telomeric DNA in Arabidopsis.

作者信息

Vespa Laurent, Couvillion Mary, Spangler Elizabeth, Shippen Dorothy E

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128, USA.

出版信息

Genes Dev. 2005 Sep 15;19(18):2111-5. doi: 10.1101/gad.1333805.

DOI:10.1101/gad.1333805
PMID:16166376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1221882/
Abstract

Here we examine the function of ATM and ATR at telomeres in Arabidopsis. Although plants lacking ATM or ATR display wild-type telomere length homeostasis, chromosome end protection is compromised in atm atr mutants. Moreover, atm tert Arabidopsis experience an abrupt, early onset of genome instability, arguing that ATM is required for protection of short telomeres. ATR, by contrast, is required for maintenance of telomeric DNA as telomere shortening is dramatically accelerated in atr tert mutants relative to tert plants. Thus, ATM and ATR make essential and distinct contributions to chromosome end protection and telomere maintenance in higher eukaryotes.

摘要

在此,我们研究了拟南芥端粒中ATM和ATR的功能。尽管缺乏ATM或ATR的植物表现出野生型端粒长度稳态,但atm atr突变体中染色体末端保护功能受损。此外,atm tert拟南芥经历了基因组不稳定的突然且早期发作,这表明ATM是保护短端粒所必需的。相比之下,ATR是维持端粒DNA所必需的,因为相对于tert植物,atr tert突变体中端粒缩短显著加速。因此,ATM和ATR对高等真核生物的染色体末端保护和端粒维持做出了重要且不同的贡献。