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J Pediatr Genet 2022; 11(04): 287-291
DOI: 10.1055/s-0041-1726282
Original Article

Exome Sequencing Reveals De Novo Variants in Congenital Scoliosis

Kohei Murakami 
1   Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
2   Laboratory of Immunology, Faculty of Veterinary Medicine, Okayama University of Science, Imabari, Ehime, Japan
,
Shingo Kikugawa
3   DNA Chip Research Inc., Minato-ku, Tokyo, Japan
,
Shoji Seki
4   Department of Orthopedic Surgery, Faculty of Medicine, University of Toyama, Toyama, Japan
,
Hidetomi Terai 
5   Department of Orthopedics, Osaka City University Graduate School of Medicine, Osaka, Japan
,
Takako Suzuki
1   Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
6   Department of Human Nutrition, Faculty of Human Nutrition, Tokyo Kasei Gakuin University, Chiyoda, Tokyo, Japan
,
Masaki Nakano
1   Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
,
Jun Takahashi
1   Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
,
Yukio Nakamura 
1   Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
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Abstract

Congenital scoliosis (CS) is a lateral curvature of the spine characterized by the presence of vertebral anomalies. Pathogenic genetic variants in the TBX6 gene are one of the causes of CS. However, since many clinically diagnosed cases of CS are without known TBX6 gene variations, this study aims to uncover new genes related to disease susceptibility of CS by exome sequencing (ES). This study employed ES in a cohort of 5 Japanese patients with CS and their healthy parents or a sister for a total of 16 samples among 5 families. Variant interpretation was performed using SIFT, PolyPhen-2, Mutation Taster, and CADD. Four de novo variants were identified by ES and confirmed by Sanger sequencing: 1 frameshift variant (SHISA3) and 3 missense variants (AGBL5, HDAC4, and PDE2A). ES also uncovered 1 homozygous variant in the MOCOS gene. All of these variants were predicted to be deleterious by SIFT, PolyPhen-2, Mutation Taster, and/or CADD. The number of de novo variants identified in this study was exactly what would be expected by chance. Additional functional studies or gathering matched patients using Gene Matcher are needed.

Keywords

congenital scoliosis - exome sequencing - de novo variants

Author Contributions

Y.N. conceptualized and designed the project. S.K. collected data and conducted the analyses. T.S. curated data. K.M., S.K., and Y.N. wrote the original draft. S.S., H.T. provided resources. M.N., J.T., Y.N. supervised all aspects of this work. All authors reviewed all data, revised the manuscript critically for intellectual content, and approved the final version for submission.




Publication History

Received: 21 October 2020

Accepted: 05 February 2021

Article published online:
14 April 2021

© 2021. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 

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