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Roles of eukaryotic topoisomerases in transcription, replication and genomic stability.真核生物拓扑异构酶在转录、复制和基因组稳定性中的作用。
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Novel TDP2-ubiquitin interactions and their importance for the repair of topoisomerase II-mediated DNA damage.新型TDP2-泛素相互作用及其对拓扑异构酶II介导的DNA损伤修复的重要性。
Nucleic Acids Res. 2016 Dec 1;44(21):10201-10215. doi: 10.1093/nar/gkw719. Epub 2016 Aug 19.
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End-processing nucleases and phosphodiesterases: An elite supporting cast for the non-homologous end joining pathway of DNA double-strand break repair.末端加工核酸酶和磷酸二酯酶:DNA双链断裂修复非同源末端连接途径的精英配角。
DNA Repair (Amst). 2016 Jul;43:57-68. doi: 10.1016/j.dnarep.2016.05.011. Epub 2016 May 18.
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Deazaflavin Inhibitors of Tyrosyl-DNA Phosphodiesterase 2 (TDP2) Specific for the Human Enzyme and Active against Cellular TDP2.针对人源酶且对细胞内TDP2具有活性的酪氨酰-DNA磷酸二酯酶2(TDP2)的脱氮黄素抑制剂
ACS Chem Biol. 2016 Jul 15;11(7):1925-33. doi: 10.1021/acschembio.5b01047. Epub 2016 May 11.
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Activity-Induced DNA Breaks Govern the Expression of Neuronal Early-Response Genes.活动诱导的DNA断裂调控神经元早期反应基因的表达。
Cell. 2015 Jun 18;161(7):1592-605. doi: 10.1016/j.cell.2015.05.032. Epub 2015 Jun 4.
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Topoisomerase-mediated chromosomal break repair: an emerging player in many games.拓扑异构酶介导的染色体断裂修复:多种游戏中的新兴角色。
Nat Rev Cancer. 2015 Mar;15(3):137-51. doi: 10.1038/nrc3892. Epub 2015 Feb 19.
7
Involvement of the host DNA-repair enzyme TDP2 in formation of the covalently closed circular DNA persistence reservoir of hepatitis B viruses.宿主DNA修复酶TDP2参与乙型肝炎病毒共价闭合环状DNA持久性储存库的形成。
Proc Natl Acad Sci U S A. 2014 Oct 7;111(40):E4244-53. doi: 10.1073/pnas.1409986111. Epub 2014 Sep 8.
8
Tyrosyl-DNA-phosphodiesterases (TDP1 and TDP2).酪氨酰-DNA磷酸二酯酶(TDP1和TDP2)。
DNA Repair (Amst). 2014 Jul;19:114-29. doi: 10.1016/j.dnarep.2014.03.020. Epub 2014 May 22.
9
Proteolytic degradation of topoisomerase II (Top2) enables the processing of Top2·DNA and Top2·RNA covalent complexes by tyrosyl-DNA-phosphodiesterase 2 (TDP2).拓扑异构酶 II(Top2)的蛋白水解降解使酪氨酸-DNA-磷酸二酯酶 2(TDP2)能够处理 Top2·DNA 和 Top2·RNA 共价复合物。
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10
Increased negative supercoiling of mtDNA in TOP1mt knockout mice and presence of topoisomerases IIα and IIβ in vertebrate mitochondria.TOP1mt基因敲除小鼠中线粒体DNA负超螺旋增加以及脊椎动物线粒体中拓扑异构酶IIα和IIβ的存在。
Nucleic Acids Res. 2014 Jun;42(11):7259-67. doi: 10.1093/nar/gku384. Epub 2014 May 6.

线粒体酪氨酸-DNA 磷酸二酯酶 2 及其 TDP2 短亚型。

Mitochondrial tyrosyl-DNA phosphodiesterase 2 and its TDP2 short isoform.

机构信息

Laboratory of Molecular Pharmacology, Developmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA

Laboratory of Molecular Pharmacology, Developmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA.

出版信息

EMBO Rep. 2018 Mar;19(3). doi: 10.15252/embr.201642139. Epub 2018 Feb 9.

DOI:10.15252/embr.201642139
PMID:29438979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5836098/
Abstract

Tyrosyl-DNA phosphodiesterase 2 (TDP2) repairs abortive topoisomerase II cleavage complexes. Here, we identify a novel short isoform of TDP2 (TDP2) expressed from an alternative transcription start site. TDP2 contains a mitochondrial targeting sequence, contributing to its enrichment in the mitochondria and cytosol, while full-length TDP2 contains a nuclear localization signal and the ubiquitin-associated domain in the N-terminus. Our study reveals that both TDP2 isoforms are present and active in the mitochondria. Comparison of isogenic wild-type () and knockout () DT40 cells shows that cells are hypersensitive to mitochondrial-targeted doxorubicin (mtDox), and that complementing cells with human restores resistance to mtDox. Furthermore, mtDox selectively depletes mitochondrial DNA in cells. Using CRISPR-engineered human cells expressing only the TDP2 isoform, we show that TDP2 also protects human cells against mtDox. Finally, lack of TDP2 in the mitochondria reduces the mitochondria transcription levels in two different human cell lines. In addition to identifying a novel TDP2 isoform, our report demonstrates the presence and importance of both TDP2 isoforms in the mitochondria.

摘要

酪氨酰-DNA 磷酸二酯酶 2(TDP2)修复拓扑异构酶 II 断裂复合物。在这里,我们鉴定了一种新型的 TDP2 短同工型(TDP2),它来自一个替代的转录起始位点表达。TDP2 包含一个线粒体靶向序列,有助于其在线粒体和细胞质中的富集,而全长 TDP2 在 N 端包含一个核定位信号和泛素相关结构域。我们的研究表明,两种 TDP2 同工型都存在于线粒体中并具有活性。比较同基因野生型()和 敲除()DT40 细胞表明,细胞对线粒体靶向阿霉素(mtDox)敏感,用人类 补充 细胞可恢复对 mtDox 的抗性。此外,mtDox 选择性地耗尽细胞中的线粒体 DNA。使用仅表达 TDP2 同工型的 CRISPR 工程化的人类细胞,我们表明 TDP2 也能保护人类细胞免受 mtDox 的侵害。最后,线粒体中 TDP2 的缺失降低了两种不同的人源细胞系中线粒体的转录水平。除了鉴定一种新型的 TDP2 同工型外,我们的报告还证明了两种 TDP2 同工型在线粒体中的存在和重要性。