[No authors listed]
The substrates of SUMO4, a novel member for the SUMO gene family, were characterized in HEK293 cells cultured under serum starvation by proteomic analysis. We identified 90 SUMO4 substrates including anti-stress proteins such as antioxidant enzymes and molecular chaperones or co-chaperones. The substrates also include proteins involved in the regulation of DNA repair and synthesis, RNA processing, protein degradation, and glucose metabolism. Several SUMO4-associated transcription factors were characterized by Western blot analyses. AP-1 was selected for in vitro conjugation assays to confirm SUMO4 sumoylation of these transcription factors. Further functional analyses of the transcription factors suggested that SUMO4 sumoylation represses AP-1 and AP-2alpha transcriptional activity, but enhances GR DNA binding capacity. These results demonstrate that SUMO4 sumoylation may play an important role in the regulation of intracellular stress.
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PDIA6, SF3B4, RACK1, PRDX4, CCT7, CCT2, SPINT2, PRDX3, STIP1, STRAP, CLIC1, ENO1, ENO2, ALDOA, CCT5, FOS, G6PD, GAPDH, PHGDH, NR3C1, PDIA3, GSTP1, STOML2, HNRNPD, HNRNPF, HNRNPH1, HNRNPL, DNAJA1, HSPA1B, HSPA5, HSPA8, HSPA9, HSPD1, ACADM, IDH1, IDH3A, IMPDH2, JUN, SUMO4, TMEM189-UBE2V1, RPSA, LDHB, ARHGDIA, LMNA, LMNB1, ACO2, PA2G4, PAFAH1B3, ATP5B, RTCB, DNAJB11, PGK1, PHB, PPA1, PRPS1, MRPS22, PSMC2, PITHD1, STAT1, STAT3, PRDX2, TFAP2A, ACTG1, TOP2A, TPM3, UBE2I, UBE2V1, VCP, VDAC1, CALR, CAT, TUBA1C, EIF3I, GMPS, ZPR1, CCT6A, TXNL1, PRDX6
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