TY - JOUR T1 - Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies JF - bioRxiv DO - 10.1101/247023 SP - 247023 AU - Charlotte Gistelinck AU - Ronald Y Kwon AU - Fransiska Malfait AU - Sofie Symoens AU - Matthew P. Harris AU - Katrin Henke AU - Shannon Fisher AU - Patrick Sips AU - Brecht Guillemyn AU - Jan Willem Bek AU - Petra Vermassen AU - Hanna De Saffel AU - MaryAnn Weis AU - Anne De Paepe AU - David R Eyre AU - Andy Willaert AU - Paul J Coucke Y1 - 2018/01/01 UR - http://biorxiv.org/content/early/2018/01/11/247023.abstract N2 - The type I collagenopathies are a group of heterogeneous connective tissue disorders, that are caused by mutations in the genes encoding type I collagen and include specific forms of Osteogenesis Imperfecta (OI) and the Ehlers-Danlos syndrome (EDS). These disorders present with a broad disease spectrum and large clinical variability of which the underlying genetic basis is still poorly understood. In this study, we systematically analyzed skeletal phenotypes in a large set of zebrafish, with diverse mutations in the genes encoding type I collagen, representing different genetic forms of human OI, and the first zebrafish model of human EDS, which harbors characteristic defects in the soft connective tissues. Furthermore, we provide insight into how zebrafish and human type I collagen are compositionally and functionally related, which is relevant in the interpretation of human type I collagen related disease models. Our studies reveal a high degree of inter-genotype variability in phenotypic expressivity that closely correlates with associated OI severity. Further, we demonstrate the potential for select mutations to give rise to variable phenotypic penetrance, mirroring the clinical variability associated with human disease pathology. Therefore, our work suggests the potential for zebrafish to aid in identifying unknown genetic modifiers and mechanisms underlying the phenotypic variability in OI and related disorders. This will improve diagnostic strategies and enable the discovery of new targetable pathways for pharmacological interventionSIGNIFICANCE STATEMENT Type I collagenopathies are a heterogenous group of connective tissue disorders, caused by genetic defects in type I collagen. Inherent to these disorders is a large clinical variability, of which the underlying molecular basis remains undefined. By systematically analyzing skeletal phenotypes in a large set of type I collagen zebrafish mutants we show that zebrafish models are able to both genocopy and phenocopy different forms of human type I collagenopathies, arguing for a similar pathogenetic basis. This study illustrates the potential of zebrafish as a tool to further dissect the molecular basis of phenotypic variability in human type I collagenopathies to improve diagnostic strategies as well as promote the discovery of new targetable pathways for pharmacological intervention of these disorders. ER -