Skip to main content
. 2020 Aug 6;11:3904. doi: 10.1038/s41467-020-17667-7

Fig. 2. NIP30 regulates REGγ through phosphorylation of its conserved binding motif.

Fig. 2

a A panel of NIP30 truncations co-expressed with flag-REGγ in 293T cells was analyzed for interaction domains by immunoprecipitation. b A summary of the interaction between REGγ and various NIP30 derivative clones (+ for binding, − for no binding). c Multiple sequence alignment showing the evolutionarily conserved, serine-rich REGγ-interacting motif in NIP30. d NIP30 is phosphorylated at 4 specific serine residues. HA-tagged NIP30 with phosphorylation-mimetic (S/D) or defective (S/A) mutations were tested for interaction with REGγ by immunoprecipitation. e Generation of NIP30 expressing cells. H1299 cells with or without REGγ (shN/shR) stably expressing NIP30 constructs (WT, 4A, or 4D) were examined for p21 expression. f H1299 cells expressing distinct NIP30 constructs were analyzed for cell proliferation by MTT assays. Data represent mean ± SEM (n = 4). g Xenograft tumors derived from H1299 cells stably expressing different NIP30 constructs (WT/4A/4D) were compared for tumor size. Quantitative results are in Supplementary Fig. 3n. Data in this figure are representative of three independent repeats. Source data are provided in a Source Data file.