Assessment of SENP3-interacting proteins in hepatocytes treated with diethylnitrosamine by BioID assay.
Assessment of SENP3-interacting proteins in hepatocytes treated with diethylnitrosamine by BioID assay.
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通过 BioID 测定评估经二乙基亚硝胺处理的肝细胞中 SENP3 相互作用蛋白
DOI:
10.1093/abbs/gmab096
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发表时间:
2021-08-31
影响因子:
3.7
通讯作者:
Yang J
中科院分区:
文献类型:
--
作者:
Chen F;Yan H;Guo C;Zhu H;Yi J;Sun X;Yang J
SUMOylation of proteins regulates cell behaviors and is reversibly removed by small ubiquitin-like modifier (SUMO)-specific proteases (SENPs). The SENP family member SENP3 is involved in SUMO2/3 deconjugation and has been reported to sense cell stress and accumulate in several human cancer cells and macrophages. We previously reported that Senp3-knockout heterozygous mice showed smaller liver, but the pertinent mechanisms of SENP3 and SUMOylated substrates remain unclear. Thus, in this study, we investigated the interacting proteins with SENP3 and the alteration in hepatocytes treated with the xenobiotic diethylnitrosamine (DEN), which is specifically transformed in the liver and induces DNA double-strand breaks. Our data revealed that a certain amount of SENP3 was present in normal, untreated hepatocytes; however, DEN treatment promoted rapid SENP3 accumulation. SENP3 was mainly localized in the nuclei, and its level was significantly increased in the cytoplasm after 2 h of DEN treatment. The application of the recent proximity-dependent biotinylation (BioID) method led to the identification of 310 SENP3-interacting proteins that were involved in not only gene transcription but also RNA splicing, protein folding, and metabolism. Furthermore, after DEN exposure for a short duration, ribosomal proteins as well as proteins associated with mitochondrial ATP synthesis, membrane transport, and bile acid synthesis, rather than DNA repair proteins, were identified. This study provides insights into the diverse regulatory roles of SENP3, and the BioID method seems to be efficient for identifying physiologically relevant insoluble proteins.
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影响因子:
16.6
作者:
Lumpkin RJ;Gu H;Zhu Y;Leonard M;Ahmad AS;Clauser KR;Meyer JG;Bennett EJ;Komives EA
通讯作者:
Komives EA
影响因子:
3.3
作者:
Castle CD;Cassimere EK;Denicourt C
通讯作者:
Denicourt C
影响因子:
21.1
作者:
Wang, Ming;Sang, Jing;Yi, Jing
通讯作者:
Yi, Jing
影响因子:
16.6
作者:
Lamoliatte, Frederic;Caron, Danielle;Thibault, Pierre
通讯作者:
Thibault, Pierre
DOI:
10.1007/978-1-62703-311-4_11
发表时间:
2013-01-01
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
Roszik, Janos;Toth, Gabor;Vereb, Gyorgy
通讯作者:
Vereb, Gyorgy