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.
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
Title and authors | Publication | Year |
---|---|---|
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Alazami syndrome with a single LARP7 variant and concurrent osteo-oto-hepato-enteric syndrome: A case of complex genetic interplay
Thouqan A, Janem A, Ghanayem R, Janem A |
Radiology Case Reports | 2025 |
Paediatric Congenital Enteropathies: Clinical and Histological Review
Arienzo F, Giovannoni I, Diamanti A, Trovato CM, De Angelis P, Imondi C, Alaggio R, Francalanci P |
Diagnostics | 2025 |
Newly Described Mutations of the UNC45A Gene in Infants with Jaundice and Pruritus.
Degtyareva A, Dokshukina A, Filippova E, Shubina J, Tolmacheva E, Sadelov I, Albegova M, Degtyarev D |
Current pediatric reviews | 2025 |
Regulation of Epithelial and Endothelial Barriers by Molecular Chaperones.
Lechuga S, Marino-Melendez A, Naydenov NG, Zafar A, Braga-Neto MB, Ivanov AI |
Cells | 2024 |
Uncovering the Relationship Between Genes and Phenotypes Beyond the Gut in Microvillus Inclusion Disease
Sun M, Pylypenko O, Zhou Z, Xu M, Li Q, Houdusse A, van IJzendoorn SC |
Cellular and Molecular Gastroenterology and Hepatology | 2024 |
Modeling the cell biology of monogenetic intestinal epithelial disorders
Kaji I, Thiagarajah JR, Goldenring JR |
The Journal of Cell Biology | 2024 |
Downregulation of V-ATPase V(0) Sector Induces Microvillus Atrophy Independently of Apical Trafficking in the Mammalian Intestine.
Bidaud-Meynard A, Bourdais A, Nicolle O, Duclos M, Saleh J, Ruemmele FM, Farin HF, Delacour D, Moshous D, Michaux G |
Cellular and Molecular Gastroenterology and Hepatology | 2024 |
Cellular and molecular basis of proximal small intestine disorders.
Bildstein T, Charbit-Henrion F, Azabdaftari A, Cerf-Bensussan N, Uhlig HH |
Nature reviews. Gastroenterology & hepatology | 2024 |
Microvillous Inclusion Disease: An Exceedingly Rare Condition With a New Treatment.
Fiedler A, Brittan K, Manatsathit W |
ACG case reports journal | 2024 |
Myosin Vb Traffics P-glycoprotein to the Apical Membrane of Intestinal Epithelial Cells
Dooley SA, Kolobova E, Burman A, Kaji I, Digrazia JR, Stubler R, Goldstein A, Packirisamy C, Coutts AW, Saqui-Salces M, Gao N, Engevik MA, Shub MD, Goldenring JR, Engevik AC |
Gastroenterology | 2024 |
An update on autophagy disorders
Dafsari HS, Martinelli D, Saffari A, Ebrahimi\u2010Fakhari D, Fanto M, Dionisi\u2010Vici C, Jungbluth H |
Journal of Inherited Metabolic Disease | 2024 |
Case report: Osteo-oto-hepato-enteric syndrome caused by UNC45A deficiency
Wang R, Wang Y, Yu R, Xu W, Zhang T, Xiao Y |
Frontiers in Genetics | 2023 |
A CRISPR screen in intestinal epithelial cells identifies novel factors for polarity and apical transport
Klee KM, Hess MW, Lohmüller M, Herzog S, Pfaller K, Müller T, Vogel GF, Huber LA |
eLife | 2023 |
The genetics of monogenic intestinal epithelial disorders.
Babcock SJ, Flores-Marin D, Thiagarajah JR |
Human Genetics | 2022 |