Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Cardinale, Christopher; Li, Dong; Tian, Lifeng; Connolly, John; March, Michael; Hou, Cuiping; Wang, Fengxiang; Snyder, James; Kim, Cecilia; Chiavacci, Rosetta; Sleiman, Patrick; Burnham, Jon; Hakonarson, Hakon
• Is Part Of: BMC musculoskeletal disorders. Volume 17:Issue 1(2016)
• Page Start: 1
• Page End: 6
• Publication Date: 2016-12
• Subjects: Whole exome sequencing -- Systemic sclerosis -- Scleroderma -- NOTCH4 -- Mendelian genetics; Musculoskeletal system -- Diseases -- Periodicals; 616.705
• DOI: 10.1186/s12891-016-1320-4
• Languages: English
• ISSNs: 1471-2474

Abstract

Abstract Background Systemic sclerosis (SSc) is a rheumatologic disease with a multifactorial etiology. Genome-wide association studies imply a polygenic, complex mode of inheritance with contributions from variation at the human leukocyte antigen locus and non-coding variation at a locus on chromosome 6p21, among other modestly impactful loci. Here we describe an 8-year-old female proband presenting with diffuse cutaneous SSc/scleroderma and a family history of SSc in a grandfather and maternal aunt. Methods We employed whole exome sequencing (WES) of three members of this family. We examined rare missense, nonsense, splice-altering, and coding indels matching an autosomal dominant inheritance model. We selected one missense variant for Sanger sequencing confirmation based on its predicted impact on gene function and location in a known SSc genetic locus. Results Bioinformatic analysis found eight candidate variants meeting our criteria. We identified a very rare missense variant in the regulatory NODP domain ofNOTCH4 located at the 6p21 locus, c.4245G > A:p.Met1415Ile, segregating with the phenotype. This allele has a frequency of 1.83 × 10−5 by the data of the Exome Aggregation Consortium. Conclusion This family suggests a novel mechanism of SSc pathogenesis in which a rare and penetrant coding variation can substantially elevate disease risk in contrast to the more modest non-coding variation typically found at this locus. These results suggest that modulation of theNOTCH4 gene might be responsible for the association signal at chromosome 6p21 in SSc.