UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.

Abstract

Variants in the UNC45A cochaperone have been recently associated with a syndrome combining diarrhea, cholestasis, deafness, and bone fragility. Yet the mechanism underlying intestinal failure in UNC45A deficiency remains unclear. Here, biallelic variants in UNC45A were identified by next-generation sequencing in 6 patients with congenital diarrhea. Corroborating in silico prediction, variants either abolished UNC45A expression or altered protein conformation. Myosin VB was identified by mass spectrometry as client of the UNC45A chaperone and was found misfolded in UNC45AKO Caco-2 cells. In keeping with impaired myosin VB function, UNC45AKO Caco-2 cells showed abnormal epithelial morphogenesis that was restored by full-length UNC45A, but not by mutant alleles. Patients and UNC45AKO 3D organoids displayed altered luminal development and microvillus inclusions, while 2D cultures revealed Rab11 and apical transporter mislocalization as well as sparse and disorganized microvilli. All those features resembled the subcellular abnormalities observed in duodenal biopsies from patients with microvillus inclusion disease. Finally, microvillus inclusions and shortened microvilli were evidenced in enterocytes from unc45a-deficient zebrafish. Taken together, our results provide evidence that UNC45A plays an essential role in epithelial morphogenesis through its cochaperone function of myosin VB and that UNC45A loss causes a variant of microvillus inclusion disease.

• Authors: Rémi Duclaux-Loras, Corinne Lebreton, Jérémy Berthelet, Fabienne Charbit-Henrion, Ophelie Nicolle, Céline Revenu des Courtils, Stephanie Waich, Taras Valovka, Anis Khiat, Marion Rabant, Caroline Racine, Ida Chiara Guerrera, Júlia Baptista, Maxime M Mahe, Michael W Hess, Béatrice Durel, Nathalie Lefort, Céline Banal, Mélanie Parisot, Cecile Talbotec, Florence Lacaille, Emmanuelle Ecochard-Dugelay, Arzu Meltem Demir, Georg F Vogel, Laurence Faivre, Astor Rodrigues, Darren Fowler, Andreas R Janecke, Thomas Müller, Lukas A Huber, Fernando Rodrigues-Lima, Frank M Ruemmele, Holm H Uhlig, Filippo Del Bene, Grégoire Michaux, Nadine Cerf-Bensussan, Marianna Parlato
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 132 Issue 10 (05 16 2022) ISSN: 1558-8238 [Electronic] United States
• PMID: 35575086 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Intracellular Signaling Peptides and Proteins
• UNC45A protein, human
• Myosin Type V

Topics

• Animals
• Caco-2 Cells
• Diarrhea, Infantile (metabolism, pathology)
• Facies
• Fetal Growth Retardation
• Hair Diseases
• Humans
• Infant
• Intracellular Signaling Peptides and Proteins (metabolism)
• Malabsorption Syndromes (metabolism)
• Microvilli (genetics, pathology)
• Mucolipidoses (genetics, metabolism, pathology)
• Myosin Type V (genetics, metabolism)
• Phenotype
• Zebrafish (genetics, metabolism)