| Literature DB >> 33497358 |
Thuy-Linh Le1, Louise Galmiche2,3, Jonathan Levy4,5, Pim Suwannarat6, Debby Mei Hellebrekers7, Khomgrit Morarach8, Franck Boismoreau9, Tom Ej Theunissen10, Mathilde Lefebvre11, Anna Pelet1, Jelena Martinovic12, Antoinette Gelot13,14, Fabien Guimiot5,15, Amanda Calleroz16, Cyril Gitiaux17, Marie Hully18, Olivier Goulet19, Christophe Chardot20, Severine Drunat4,5, Yline Capri4, Christine Bole-Feysot21, Patrick Nitschké22, Sandra Whalen23, Linda Mouthon24, Holly E Babcock25, Robert Hofstra26, Irenaeus Fm de Coo27, Anne-Claude Tabet4,28, Thierry J Molina3,29, Boris Keren24, Alice Brooks26, Hubert Jm Smeets27, Ulrika Marklund8, Christopher T Gordon1, Stanislas Lyonnet1,30, Jeanne Amiel1,30, Nadège Bondurand1.
Abstract
Hirschsprung disease (HSCR) is the most frequent developmental anomaly of the enteric nervous system, with an incidence of 1 in 5000 live births. Chronic intestinal pseudo-obstruction (CIPO) is less frequent and classified as neurogenic or myogenic. Isolated HSCR has an oligogenic inheritance with RET as the major disease-causing gene, while CIPO is genetically heterogeneous, caused by mutations in smooth muscle-specific genes. Here, we describe a series of patients with developmental disorders including gastrointestinal dysmotility, and investigate the underlying molecular bases. Trio-exome sequencing led to the identification of biallelic variants in ERBB3 and ERBB2 in 8 individuals variably associating HSCR, CIPO, peripheral neuropathy, and arthrogryposis. Thorough gut histology revealed aganglionosis, hypoganglionosis, and intestinal smooth muscle abnormalities. The cell type-specific ErbB3 and ErbB2 function was further analyzed in mouse single-cell RNA sequencing data and in a conditional ErbB3-deficient mouse model, revealing a primary role for ERBB3 in enteric progenitors. The consequences of the identified variants were evaluated using quantitative real-time PCR (RT-qPCR) on patient-derived fibroblasts or immunoblot assays on Neuro-2a cells overexpressing WT or mutant proteins, revealing either decreased expression or altered phosphorylation of the mutant receptors. Our results demonstrate that dysregulation of ERBB3 or ERBB2 leads to a broad spectrum of developmental anomalies, including intestinal dysmotility.Entities:
Keywords: Development; Gastroenterology; Genetic diseases; Molecular genetics
Year: 2021 PMID: 33497358 PMCID: PMC7954599 DOI: 10.1172/JCI145837
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808