Mutations and variants of ONECUT1 in diabetes

Item Type:	Article
Title:	Mutations and variants of ONECUT1 in diabetes
Creators Name:	Philippi, A. and Heller, S. and Costa, I.G. and Senée, V. and Breunig, M. and Li, Z. and Kwon, G. and Russell, R. and Illing, A. and Lin, Q. and Hohwieler, M. and Degavre, A. and Zalloua, P. and Liebau, S. and Schuster, M. and Krumm, Jo. and Zhang, X. and Geusz, R. and Benthuysen, J. R. and Wang, A. and Chiou, J. and Gaulton, K. and Neubauer, H. and Simon, E. and Klein, T. and Wagner, M. and Nair, G. and Besse, C. and Dandine-Roulland, C. and Olaso, R. and Deleuze, J.F. and Kuster, B. and Hebrok, M. and Seufferlein, T. and Sander, M. and Boehm, B.O. and Oswald, F. and Nicolino, M. and Julier, C. and Kleger, A.
Abstract:	Genes involved in distinct diabetes types suggest shared disease mechanisms. Here we show that One Cut Homeobox 1 (ONECUT1) mutations cause monogenic recessive syndromic diabetes in two unrelated patients, characterized by intrauterine growth retardation, pancreas hypoplasia and gallbladder agenesis/hypoplasia, and early-onset diabetes in heterozygous relatives. Heterozygous carriers of rare coding variants of ONECUT1 define a distinctive subgroup of diabetic patients with early-onset, nonautoimmune diabetes, who respond well to diabetes treatment. In addition, common regulatory ONECUT1 variants are associated with multifactorial type 2 diabetes. Directed differentiation of human pluripotent stem cells revealed that loss of ONECUT1 impairs pancreatic progenitor formation and a subsequent endocrine program. Loss of ONECUT1 altered transcription factor binding and enhancer activity and NKX2.2/NKX6.1 expression in pancreatic progenitor cells. Collectively, we demonstrate that ONECUT1 controls a transcriptional and epigenetic machinery regulating endocrine development, involved in a spectrum of diabetes, encompassing monogenic (recessive and dominant) as well as multifactorial inheritance. Our findings highlight the broad contribution of ONECUT1 in diabetes pathogenesis, marking an important step toward precision diabetes medicine.
Keywords:	Cell Differentiation, Congenital Abnormalities, Fetal Growth Retardation, Gallbladder, Genetic Transcription, Hepatocyte Nuclear Factor 6, Homeobox Protein Nkx-2.2, Homeodomain Proteins, Multifactorial Inheritance, Organogenesis, Pancreas, Pancreatic Diseases, Pluripotent Stem Cells, Type 2 Diabetes Mellitus
Source:	Nature Medicine
ISSN:	1078-8956
Publisher:	Nature Publishing Group
Volume:	27
Number:	11
Page Range:	1928-1940
Date:	November 2021
Official Publication:	https://doi.org/10.1038/s41591-021-01502-7
PubMed:	View item in PubMed

Repository Staff Only: item control page