| Literature DB >> 31834374 |
Christopher C Y Mak1, Dan Doherty2,3, Angela E Lin4, Nancy Vegas5,6, Megan T Cho7, Géraldine Viot8, Clémantine Dimartino5,6, James D Weisfeld-Adams9, Davor Lessel10, Shelagh Joss11, Chumei Li12, Claudia Gonzaga-Jauregui13, Yuri A Zarate14, Nadja Ehmke15, Denise Horn15, Caitlin Troyer16, Sarina G Kant17, Youngha Lee18, Gisele E Ishak3,19, Gordon Leung1, Amanda Barone Pritchard20, Sandra Yang7, Eric G Bend21,22, Francesca Filippini5,6, Chelsea Roadhouse12, Nicolas Lebrun23, Michele G Mehaffey2, Pierre-Marie Martin24,25, Benjamin Apple9, Francisca Millan7, Oliver Puk26, Mariette J V Hoffer17, Lindsay B Henderson7, Ruth McGowan11, Ingrid M Wentzensen7, Steven Pei1, Farah R Zahir27, Mullin Yu1, William T Gibson27, Ann Seman28, Marcie Steeves4, Jill R Murrell29, Sabine Luettgen10, Elizabeth Francisco30, Tim M Strom31,32, Louise Amlie-Wolf33, Angela M Kaindl34,35, William G Wilson16, Sara Halbach36, Lina Basel-Salmon37,38,39,40, Noa Lev-El37, Jonas Denecke41, Lisenka E L M Vissers42, Kelly Radtke43, Jamel Chelly44,45,46, Elaine Zackai20,47, Jan M Friedman27, Michael J Bamshad2,48,49, Deborah A Nickerson48,49, Russell R Reid50, Koenraad Devriendt51, Jong-Hee Chae52, Elliot Stolerman21, Carey McDougall20, Zöe Powis43, Thierry Bienvenu23,53, Tiong Y Tan54, Naama Orenstein38,39, William B Dobyns2,3,55, Joseph T Shieh24,25, Murim Choi18,52, Darrel Waggoner36, Karen W Gripp33, Michael J Parker56, Joan Stoler28, Stanislas Lyonnet5,6,57, Valérie Cormier-Daire6,57,58, David Viskochil59, Trevor L Hoffman60, Jeanne Amiel5,6,57, Brian H Y Chung1, Christopher T Gordon5,6.
Abstract
MN1 encodes a transcriptional co-regulator without homology to other proteins, previously implicated in acute myeloid leukaemia and development of the palate. Large deletions encompassing MN1 have been reported in individuals with variable neurodevelopmental anomalies and non-specific facial features. We identified a cluster of de novo truncating mutations in MN1 in a cohort of 23 individuals with strikingly similar dysmorphic facial features, especially midface hypoplasia, and intellectual disability with severe expressive language delay. Imaging revealed an atypical form of rhombencephalosynapsis, a distinctive brain malformation characterized by partial or complete loss of the cerebellar vermis with fusion of the cerebellar hemispheres, in 8/10 individuals. Rhombencephalosynapsis has no previously known definitive genetic or environmental causes. Other frequent features included perisylvian polymicrogyria, abnormal posterior clinoid processes and persistent trigeminal artery. MN1 is encoded by only two exons. All mutations, including the recurrent variant p.Arg1295* observed in 8/21 probands, fall in the terminal exon or the extreme 3' region of exon 1, and are therefore predicted to result in escape from nonsense-mediated mRNA decay. This was confirmed in fibroblasts from three individuals. We propose that the condition described here, MN1 C-terminal truncation (MCTT) syndrome, is not due to MN1 haploinsufficiency but rather is the result of dominantly acting C-terminally truncated MN1 protein. Our data show that MN1 plays a critical role in human craniofacial and brain development, and opens the door to understanding the biological mechanisms underlying rhombencephalosynapsis.Entities:
Keywords: MCTT syndrome; MN1; craniofacial development; intellectual disability; rhombencephalosynapsis
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Year: 2020 PMID: 31834374 PMCID: PMC7962909 DOI: 10.1093/brain/awz379
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501