Reduced penetrance in a large Caucasian pedigree with Stickler syndrome: Influence Statistics

Expert Impact

Concepts for which they have has direct influence: Stickler syndrome , Exome sequencing , Exon 2 , 2 col2a1 , Connective tissue , Sensorineural humans , Hearing loss .

Key People For Stickler Syndrome

Top KOLs in the world
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Martin Paul Snead
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John R W Yates
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John D Scott
stickler syndrome retinal detachment vitreous phenotype
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Allan James Richards
stickler syndrome retinal detachment type iii collagen
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Ruth M Liberfarb
stickler syndrome spinal abnormalities dna polymorphisms
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A G STEINBERG
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Reduced penetrance in a large Caucasian pedigree with Stickler syndrome

Abstract

. BACKGROUND: In a four-generation Caucasian family variably diagnosed with autosomal dominant (AD) Stickler or Wagner disease, commercial gene screening failed to identify a mutation in COL2A1 or VCAN. We utilized linkage mapping and exome sequencing to identify the causal variant. MATERIALS AND METHODS: Genomic DNA samples collected from 40 family members were analyzed. A whole-genome linkage scan was performed using Illumina HumanLinkage-24 BeadChip followed by two-point and multipoint linkage analyses using FASTLINK and MERLIN. Exome sequencing was performed on two affected individuals, followed by co-segregation analysis. RESULTS: Parametric multipoint linkage analysis using an AD inheritance model demonstrated HLOD scores > 2.00 at chromosomes 1p36.13-1p36.11 and 12q12-12q14.1. SIMWALK multipoint analysis replicated the peak in chromosome 12q (peak LOD = 1.975). FASTLINK two-point analysis highlighted several clustered chromosome 12q SNPs with HLOD > 1.0. Exome sequencing revealed a novel nonsense mutation (c.115C>T, p.Gln39*) in exon 2 of COL2A1 that is expected to result in nonsense-mediated decay of the RNA transcript. This mutation co-segregated with all clinically affected individuals and seven individuals who were clinically unaffected. CONCLUSIONS: The utility of combining traditional linkage mapping and exome sequencing is highlighted to identify gene mutations in large families displaying a Mendelian inheritance of disease. Historically, nonsense mutations in exon 2 of COL2A1 have been reported to cause a fully penetrant ocular-only Stickler phenotype with few or no systemic manifestations. We report a novel nonsense mutation in exon 2 of COL2A1 that displays incomplete penetrance and/or variable age of onset with extraocular manifestations.