The Mediator complex regulates protein-coding gene transcription by coordinating the interaction of upstream enhancers with the basal transcription machinery at the promoter. Pathogenic variants in Mediator subunits typically lead to neurodevelopmental or neurodegenerative disorders with variable clinical presentations, designated as MEDopathies. Here, we report the identification of 25 individuals from 18 families with bi-allelic MED16 variants who have a multiple congenital anomalies (MCAs)-intellectual disability syndrome. Intellectual disability, speech delay, and/or motor delay of variable severity were constant and associated with variable combinations of craniofacial defects (micro/retrognathia, cleft palate, and preauricular tags), anomalies of the extremities, and heart defects (predominantly tetralogy of Fallot). Visual impairment, deafness, and magnetic resonance imaging (MRI) abnormalities were also frequent. The 26 variants identified were comprised of eight predicted protein-truncating (three intragenic deletions, two frameshifts, and one nonsense and two essential splice site variants) and 18 missense or in-frame duplication variants affecting conserved residues, without clear correlation between phenotypic severity and variant type combination. Three-dimensional modeling indicated that the missense and duplication variants likely have a destabilizing effect on the structural elements of the protein. Immunofluorescence assays demonstrated protein mislocalization from the nucleus to the cytoplasm for 16 of the 17 variants studied. Homozygous mutant med16 zebrafish presented growth delay and increased mortality compared with wild-type fish, and Med16 knockout mice are preweaning lethal, highlighting the conserved requirement of MED16 for development. Overall, we describe an autosomal recessive MCAs-intellectual disability MEDopathy, emphasizing the importance of Mediator during neurodevelopment and suggesting that some tissues are particularly sensitive to the loss of certain subunits.
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations.
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作者:Guillouet Charlotte, Agostini Valeria, Baujat Geneviève, Cocciadiferro Dario, Pippucci Tommaso, Lesieur-Sebellin Marion, Georget Mathieu, Schatz Ulrich, Fauth Christine, Louie Raymond J, Rogers Curtis, Davis Jessica M, Konstantopoulou Vassiliki, Mayr Johannes A, Bouman Arjan, Wilke Martina, VanNoy Grace E, England Eleina M, Park Kristen L, Brown Kathleen, Saenz Margarita, Novelli Antonio, Digilio Maria Cristina, Mastromoro Gioia, Rongioletti Mauro Ciro Antonio, Piacentini Gerardo, Kaiyrzhanov Rauan, Guliyeva Sughra, Hasanova Lala, Shears Deborah, Bhatnagar Ishita, Stals Karen, Klaas Oliver, Horvath Judit, Bouvagnet Patrice, Witmer P Dane, MacCarrick Gretchen, Cisarova Katarina, Good Jean-Marc, Gorokhova Svetlana, Boute Odile, Smol Thomas, Bruel Ange-Line, Patat Olivier, Broadbent Julia R, Tan Tiong Y, Tan Natalie B, Lyonnet Stanislas, Busa Tiffany, Graziano Claudio, Amiel Jeanne, Gordon Christopher T
| 期刊: | American Journal of Human Genetics | 影响因子: | 8.100 |
| 时间: | 2025 | 起止号: | 2025 Apr 3; 112(4):829-845 |
| doi: | 10.1016/j.ajhg.2025.02.016 | ||
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