Molecular and cellular endocrinology · 2015
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD).
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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McCabe Mark J, Hu Youli, Gregory Louise C, Gaston-Massuet Carles, Alatzoglou Kyriaki S, Saldanha José W, Gualtieri Angelica, Thankamony Ajay, Hughes Ieuan, Townshend Sharron, Martinez-Barbera Juan-Pedro, Bouloux Pierre-Marc, Dattani Mehul T
Аннотация
KAL1 is implicated in 5% of Kallmann syndrome cases, a disorder which genotypically overlaps with septo-optic dysplasia (SOD). To date, a reporter-based assay to assess the functional consequences of KAL1 mutations is lacking. We aimed to develop a luciferase assay for novel application to functional assessment of rare KAL1 mutations detected in a screen of 422 patients with SOD. Quantitative analysis was performed using L6-myoblasts stably expressing FGFR1, transfected with a luciferase-reporter vector containing elements of the FGF-responsive osteocalcin promoter. The two variants assayed [p.K185N, p.P291T], were detected in three females with SOD (presenting with optic nerve hypoplasia, midline and pituitary defects). Our novel assay revealed significant decreases in transcriptional activity [p.K185N: 21% (p < 0.01); p.P291T: 40% (p < 0.001)]. Our luciferase-reporter assay, developed for assessment of KAL1 mutations, determined that two variants in females with hypopituitarism/SOD are loss-of-function; demonstrating that this assay is suitable for quantitative assessment of mutations in this gene.