دورية أكاديمية

Transcriptional Activity of the Islet β Cell Factor Pdx1 is Augmented by Lysine Methylation Catalyzed by the Methyltransferase Set7/9

التفاصيل البيبلوغرافية
العنوان: Transcriptional Activity of the Islet β Cell Factor Pdx1 is Augmented by Lysine Methylation Catalyzed by the Methyltransferase Set7/9
المؤلفون: Maganti, Aarthi V., Maier, Bernhard, Tersey, Sarah A., Sampley, Megan L., Mosley, Amber L., Özcan, Sabire, Pachaiyappan, Boobalan, Woster, Patrick M., Hunter, Chad S., Stein, Roland, Mirmira, Raghavendra G.
المساهمون: Department of Cellular & Integrative Physiology, IU School of Medicine
المصدر: Publisher
سنة النشر: 2015
المجموعة: Indiana University - Purdue University Indianapolis: IUPUI Scholar Works
مصطلحات موضوعية: pancreatic islet, protein methylation, diabetes, gene knockout
الوصف: The transcription factor Pdx1 is crucial to islet β cell function and regulates target genes in part through interaction with coregulatory factors. Set7/9 is a Lys methyltransferase that interacts with Pdx1. Here we tested the hypothesis that Lys methylation of Pdx1 by Set7/9 augments Pdx1 transcriptional activity. Using mass spectrometry and mutational analysis of purified proteins, we found that Set7/9 methylates the N-terminal residues Lys-123 and Lys-131 of Pdx1. Methylation of these residues occurred only in the context of intact, full-length Pdx1, suggesting a specific requirement of secondary and/or tertiary structural elements for catalysis by Set7/9. Immunoprecipitation assays and mass spectrometric analysis using β cells verified Lys methylation of endogenous Pdx1. Cell-based luciferase reporter assays using wild-type and mutant transgenes revealed a requirement of Pdx1 residue Lys-131, but not Lys-123, for transcriptional augmentation by Set7/9. Lys-131 was not required for high-affinity interactions with DNA in vitro, suggesting that its methylation likely enhances post-DNA binding events. To define the role of Set7/9 in β cell function, we generated mutant mice in which the gene encoding Set7/9 was conditionally deleted in β cells (SetΔβ). SetΔβ mice exhibited glucose intolerance similar to Pdx1-deficient mice, and their isolated islets showed impaired glucose-stimulated insulin secretion with reductions in expression of Pdx1 target genes. Our results suggest a previously unappreciated role for Set7/9-mediated methylation in the maintenance of Pdx1 activity and β cell function.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: Journal of Biological Chemistry; Maganti, A. V., Maier, B., Tersey, S. A., Sampley, M. L., Mosley, A. L., Özcan, S., . & Mirmira, R. G. (2015). Transcriptional Activity of the Islet β Cell Factor Pdx1 Is Augmented by Lysine Methylation Catalyzed by the Methyltransferase Set7/9. Journal of Biological Chemistry, 290(15), 9812-9822.; https://hdl.handle.net/1805/6616Test
الإتاحة: https://hdl.handle.net/1805/6616Test
حقوق: IUPUI Open Access Policy
رقم الانضمام: edsbas.CE4CEA82
قاعدة البيانات: BASE