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