Journal Article

Nuclear accumulation of UBC9 contributes to SUMOylation of lamin A/C and nucleophagy in response to DNA damage

Gao, Ning, Jiang, Xiuxing, Li, Lirong, Hu, Xiaoye, Liu, Yanxia, Li, Yunong, Gao, Ziyi, Hu, Jinjiao, Shi, Jingshan, Zhang, Yanhao

2019

Overview

Background Macroautophagy (hereafter referred to as autophagy) is an evolutionarily conserved intracellular mechanism for lysosomal degradation of damaged cellular components. The specific degradation of nuclear components by the autophagy pathway is called nucleophagy. Most studies have focused on autophagic turnover of cytoplasmic materials, and little is known about the role of autophagy in the degradation of nuclear components. Methods Human MDA-MB-231 and MCF-7 breast cancer cell lines were used as model systems in vitro. Induction of nucleophagy by nuclear DNA leakage was determined by western blot and immunofluorescence analyses. The interaction and colocalization of LC3 and lamin A/C was determined by immunoprecipitation and immunofluorescence. The role of the SUMO E2 ligase, UBC9, on the regulation of SUMOylation of lamin A/C and nucleophagy was determined by siRNA silencing of UBC9, and analyzed by immunoprecipitation and immunofluorescence. Results DNA damage induced nuclear accumulation of UBC9 ligase which resulted in SUMOylation of lamin A/C and that SUMOylation of this protein was required for the interaction between the autophagy protein LC3 and lamin A/C, which was required for nucleophagy. Knockdown of UBC9 prevented SUMOylation of lamin A/C and LC3-lamin A/C interaction. This attenuated nucleophagy which degraded nuclear components lamin A/C and leaked nuclear DNA mediated by DNA damage. Conclusions Our findings suggest that nuclear DNA leakage activates nucleophagy through UBC9-mediated SUMOylation of lamin A/C, leading to degradation of nuclear components including lamin A/C and leaked nuclear DNA.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: A549 Cells / Analysis / Apoptosis / Autophagy / Autophagy - physiology / Biomedical and Life Sciences / Biomedicine / Breast cancer / Breast Neoplasms - drug therapy / Breast Neoplasms - genetics / Breast Neoplasms - metabolism / Cancer / Cancer Research / Cell Line, Tumor / Cell Nucleus - metabolism / Deoxyribonucleic acid / DNA / DNA Damage / Doxorubicin - pharmacology / Fluorescent antibody technique / Gene expression / Genetic research / HEK293 Cells / Hep G2 Cells / Humans / Immunology / Lamin A/C / Lamin Type A - genetics / Lamin Type A - metabolism / Lamins - genetics / Lamins - metabolism / LC3 / Ligases / Localization / MCF-7 Cells / Microscopy, Confocal / Mutation / Nucleophagy / Oncology / Plasmids / Proteins / SUMOylation / Tumorigenesis / UBC9 / Ubiquitin-Conjugating Enzymes - genetics / Ubiquitin-Conjugating Enzymes - metabolism