Takumi Nakamura1,2, Kotori Jimbo3, Kazuo Nakajima2, Takashi Tsuboi1, Tadafumi Kato2. 1. Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo, Japan. 2. Laboratory for Molecular Dynamics of Mental Disorders, RIKEN Center for Brain Science, Wako, Japan. 3. Faculty of Medicine, Nara Medical University, Kashihara, Japan.
Abstract
AIM: We previously performed the first trio-based exome study for bipolar disorder and identified 71 de novo mutations. Among these mutations, the only mutation located at the splice donor site was in UNC13B. We focused on and analyzed the functions of the mutation. METHODS: In order to analyze the functional alterations, due to the mutation, we performed a minigene splicing assay. KEY RESULTS: We found that the mutation caused the loss of a wild-type splicing variant, which was consistent with the computational splice prediction, and that an exon-skipping variant increased significantly. The exon-skipping variant also existed in the wild-type minigene, although it was rare. Hence, we validated the expression of the exon-skipping variant using total RNAs derived from the human cerebral cortex. We showed the possibility that the exon-skipping variant was rare, but expressed even in those that do not carry the mutation. CONCLUSIONS: Based on our results, we suggest that an abnormal splicing pattern of UNC13B occurred in the patient, which could be related to the pathophysiology of bipolar disorder.
AIM: We previously performed the first trio-based exome study for bipolar disorder and identified 71 de novo mutations. Among these mutations, the only mutation located at the splice donor site was in UNC13B. We focused on and analyzed the functions of the mutation. METHODS: In order to analyze the functional alterations, due to the mutation, we performed a minigene splicing assay. KEY RESULTS: We found that the mutation caused the loss of a wild-type splicing variant, which was consistent with the computational splice prediction, and that an exon-skipping variant increased significantly. The exon-skipping variant also existed in the wild-type minigene, although it was rare. Hence, we validated the expression of the exon-skipping variant using total RNAs derived from the human cerebral cortex. We showed the possibility that the exon-skipping variant was rare, but expressed even in those that do not carry the mutation. CONCLUSIONS: Based on our results, we suggest that an abnormal splicing pattern of UNC13B occurred in the patient, which could be related to the pathophysiology of bipolar disorder.
Authors: Farid Rajabli; Briseida E Feliciano-Astacio; Holly N Cukier; Liyong Wang; Anthony J Griswold; Kara L Hamilton-Nelson; Larry D Adams; Vanessa C Rodriguez; Pedro R Mena; Sergio Tejada; Katrina Celis; Patrice L Whitehead; Derek J Van Booven; Natalia K Hofmann; Parker L Bussies; Michael Prough; Angel Chinea; Nereida I Feliciano; Badri N Vardarajan; Christiane Reitz; Joseph H Lee; Martin J Prince; Ivonne Z Jimenez; Richard P Mayeux; Heriberto Acosta; Clifton L Dalgard; Jonathan L Haines; Jeffery M Vance; Michael L Cuccaro; Gary W Beecham; Margaret A Pericak-Vance Journal: Neurobiol Aging Date: 2021-02-28 Impact factor: 5.133