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Citations to this article

UNC45A deficiency causes microvillus inclusion disease–like phenotype by impairing myosin VB–dependent apical trafficking
Rémi Duclaux-Loras, … , Nadine Cerf-Bensussan, Marianna Parlato
Rémi Duclaux-Loras, … , Nadine Cerf-Bensussan, Marianna Parlato
Published May 16, 2022
Citation Information: J Clin Invest. 2022;132(10):e154997. https://doi.org/10.1172/JCI154997.
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Research Article Gastroenterology Article has an altmetric score of 10

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

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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

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Total citations by year

Year: 2025 2024 2023 2022 Total
Citations: 4 8 2 1 15
Citation information
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Citations to this article (15)

Title and authors Publication Year
Altered Chaperone-Non-Muscle Myosin II Interactions Drive Pathogenicity of the UNC45A c.710T>C Variant in Osteo-Oto-Hepato-Enteric Syndrome
Stephanie Waich, Karin Kreidl, Julia Vodopiutz, Arzu Meltem Demir, Adam R Pollio, Vojtěch Dostál, Kristian Pfaller, Marianna Parlato, Nadine Cerf-Bensussan, Rüdiger Adam, Georg F Vogel, Holm H. Uhlig, Frank Ruemmele, Thomas Müller, Michael W. Hess, Andreas Janecke, Lukas A. Huber, Taras Valovka
JCI Insight 2025
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

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