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Publication : LIM-domain transcription complexes interact with ring-finger ubiquitin ligases and thereby impact islet β-cell function.

First Author  Wade AK Year  2019
Journal  J Biol Chem Volume  294
Issue  31 Pages  11728-11740
PubMed ID  31186351 Mgi Jnum  J:281142
Mgi Id  MGI:6369128 Doi  10.1074/jbc.RA118.006985
Citation  Wade AK, et al. (2019) LIM-domain transcription complexes interact with ring-finger ubiquitin ligases and thereby impact islet beta-cell function. J Biol Chem 294(31):11728-11740
abstractText  Diabetes is characterized by a loss of beta-cell mass, and a greater understanding of the transcriptional mechanisms governing beta-cell function is required for future therapies. Previously, we reported that a complex of the Islet-1 (Isl1) transcription factor and the co-regulator single-stranded DNA-binding protein 3 (SSBP3) regulates the genes necessary for beta-cell function, but few proteins are known to interact with this complex in beta-cells. To identify additional components, here we performed SSBP3 reverse-cross-linked immunoprecipitation (ReCLIP)- and MS-based experiments with mouse beta-cell extracts and compared the results with those from our previous Isl1 ReCLIP study. Our analysis identified the E3 ubiquitin ligases ring finger protein 20 (RNF20) and RNF40, factors that in nonpancreatic cells regulate transcription through imparting monoubiquitin marks on histone H2B (H2Bub1), a precursor to histone H3 lysine 4 trimethylation (H3K4me3). We hypothesized that RNF20 and RNF40 regulate similar genes as those regulated by Isl1 and SSBP3 and are important for beta-cell function. We observed that Rnf20 and Rnf40 depletion reduces beta-cell H2Bub1 marks and uncovered several target genes, including glucose transporter 2 (Glut2), MAF BZIP transcription factor A (MafA), and uncoupling protein 2 (Ucp2). Strikingly, we also observed that Isl1 and SSBP3 depletion reduces H2Bub1 and H3K4me3 marks, suggesting that they have epigenetic roles. We noted that the RNF complex is required for glucose-stimulated insulin secretion and normal mitochondrial reactive oxygen species levels. These findings indicate that RNF20 and RNF40 regulate beta-cell gene expression and insulin secretion and establish a link between Isl1 complexes and global cellular epigenetics.
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