DNA damage-induced translocation of mitochondrial factor HIGD1A into the nucleus regulates homologous recombination and radio/chemo-sensitivity
文献类型：期刊论文
| 作者 | Chen, Bin1,2,3; Xu, Feng1,2,3; Gao, Yang1,2,3; Hu, Guanshuo1,2,3; Zhu, Kaili1,2,3; Lu, Huayi4; Xu, An1,2 ; Chen, Shaopeng1,2; Wu, Lijun1,2,5; Zhao, Guoping1,2
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| 刊名 | ONCOGENE
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| 出版日期 | 2022-02-12 |
| ISSN号 | 0950-9232 |
| DOI | 10.1038/s41388-022-02226-9 |
| 通讯作者 | Zhao, Guoping(gpz@ipp.ac.cn) |
| 英文摘要 | HIGD1A is an important mitochondrial protein recently shown to have a novel nuclear localization under severe stress. However, whether this protein is also associated with the DNA damage response has rarely been studied. Here, we reported that DSBs-induced the translocation of mitochondrial HIGD1A to the nucleus is dependent on nuclear pore complex (NPCs), which finally promotes HR and radio/chemo-resistance. Importantly, NUP93 and HIGD1A physically interact and the interaction domain with NUP93 is located at residues 46-60 of HIGD1A. Chromatin-enriched HIGD1A can then directly interact with RPA. During the early stages of HR, HIGD1A promotes the loading of RPA to DSBs and activates the DNA damage-dependent chromatin association of RAD9-RAD1-HUS1 complex (9-1-1), which stimulates the ATR-Chk1-dependent G2/M DNA damage checkpoint. After facilitating RPA-ssDNA binding, HIGD1A in turn inhibits abnormal persistence of RPA1 foci by promoting ubiquitination of RPA1 and inducing its eventual proteasomal degradation. In addition, we have identified clinical drug Preveon associated with the HIGD1A-NUP93 interaction domain using a virtual screening approach. This compound directly interacted with HIGD1A, which was verified by NMR, and then inhibited HIGD1A translocation. Collectively, we demonstrate a novel role for HIGD1A in DSBs and provide rationale for using HIGD1A inhibitors as cancer therapeutics. |
| WOS关键词 | STRAND BREAK REPAIR ; PROTEIN-A RPA ; REPLICATION ; RAD51 ; IDENTIFICATION ; INHIBITORS ; DYNAMICS ; SITES ; SSDNA |
| 资助项目 | National Science Fund for Excellent Young Scholars[12122510] ; National Natural Science Foundation of China[32171240] ; National Natural Science Foundation of China[11835014] ; National Natural Science Foundation of China[31870845] ; HFIPS Director's Fund[YZJJZX202014] ; CAS Pioneer Hundred Talents Program |
| WOS研究方向 | Biochemistry & Molecular Biology ; Oncology ; Cell Biology ; Genetics & Heredity |
| 语种 | 英语 |
| WOS记录号 | WOS:000754368500002 |
| 出版者 | SPRINGERNATURE |
| 资助机构 | National Science Fund for Excellent Young Scholars ; National Natural Science Foundation of China ; HFIPS Director's Fund ; CAS Pioneer Hundred Talents Program |
| 源URL | [http://ir.hfcas.ac.cn:8080/handle/334002/127494]  |
| 专题 | 中国科学院合肥物质科学研究院 |
| 通讯作者 | Zhao, Guoping |
| 作者单位 | 1.Chinese Acad Sci, High Magnet Field Lab, Key Lab High Magnet Field & Ion Beam Phys Biol, Hefei 230031, Anhui, Peoples R China 2.Chinese Acad Sci, Hefei Inst Phys Sci, Anhui Prov Key Lab Environm Toxicol & Pollut Cont, Hefei 230031, Anhui, Peoples R China 3.Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China 4.Univ Sci & Technol China, Affiliated Hosp 1, Div Life Sci & Med, USTC, Hefei 230001, Anhui, Peoples R China 5.Anhui Univ, Inst Phys Sci, Informat Mat & Intelligent Sensing Lab Anhui Prov, Hefei 230601, Anhui, Peoples R China |
| 推荐引用方式 GB/T 7714 | Chen, Bin,Xu, Feng,Gao, Yang,et al. DNA damage-induced translocation of mitochondrial factor HIGD1A into the nucleus regulates homologous recombination and radio/chemo-sensitivity[J]. ONCOGENE,2022. |
| APA | Chen, Bin.,Xu, Feng.,Gao, Yang.,Hu, Guanshuo.,Zhu, Kaili.,...&Zhao, Guoping.(2022).DNA damage-induced translocation of mitochondrial factor HIGD1A into the nucleus regulates homologous recombination and radio/chemo-sensitivity.ONCOGENE. |
| MLA | Chen, Bin,et al."DNA damage-induced translocation of mitochondrial factor HIGD1A into the nucleus regulates homologous recombination and radio/chemo-sensitivity".ONCOGENE (2022). |
入库方式： OAI收割
来源：合肥物质科学研究院
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