A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development
- Am J Hum Genet. 2019 May 2;104(5):985-989. doi: 10.1016/j.ajhg.2019.03.018.
- 1. Institute of Biomedical and Clinical Science, University of Exeter Medical School, EX2 5DW Exeter, UK.
- 2. Wellcome Sanger Institute, CB10 1SA Hinxton, UK.
- 3. Centre for Anatomy and Cell Biology & MIC, Medical University of Vienna, 1090 Vienna, Austria.
- 4. Institute of Human Genetics, Christian-Albrechts-University 24105 Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
- 5. Institute of Human Genetics, Christian-Albrechts-University 24105 Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany; Institute of Human Genetics, Ulm University & Ulm University Medical Center, 89081 Ulm, Germany.
- 6. Department of Pediatrics, Division of Pediatric Endocrinology and Diabetes, Christian-Albrechts-University 24105 Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
- 7. Paediatric Endocrinology Department, Mafraq Hospital, 2951 Abu Dhabi, United Arab Emirates.
- 8. The Francis Crick Institute, NW1 1ST London, UK.
- 9. Vrije Universiteit Brussel, 1090 Brussels, Belgium; Universitair Ziekenhuis Brussel, 1090 Brussels, Belgium.
- 10. Vrije Universiteit Brussel, 1090 Brussels, Belgium.
- 11. Institute of Biomedical and Clinical Science, University of Exeter Medical School, EX2 5DW Exeter, UK. Electronic address: [email protected].
- 12. Wellcome Sanger Institute, CB10 1SA Hinxton, UK. Electronic address: [email protected].
We report a recurrent CNOT1 de novo missense mutation, GenBank: NM_016284.4; c.1603C>T (p.Arg535Cys), resulting in a syndrome of pancreatic agenesis and abnormal forebrain development in three individuals and a similar phenotype in mice. CNOT1 is a transcriptional repressor that has been suggested as being critical for maintaining embryonic stem cells in a pluripotent state. These findings suggest that CNOT1 plays a critical role in pancreatic and neurological development and describe a novel genetic syndrome of pancreatic agenesis and holoprosencephaly.