Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome

• Published in: Nature communications Vol. 6; no. 1; p. 7092
• Main Authors: Taylor, S. Paige, Dantas, Tiago J., Duran, Ivan, Wu, Sulin, Lachman, Ralph S., Nelson, Stanley F., Cohn, Daniel H., Vallee, Richard B., Krakow, Deborah
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 16.06.2015; Nature Publishing Group
• Subjects: 13/1; 13/106; 13/109; 13/51; 13/89; 14/1; 14/19; 631/208/2489/144; 631/80/128/1383; 631/80/86; 692/699/1670/427; Biological Transport - genetics; Cilia - metabolism; Cytoplasmic Dyneins - genetics; Cytoskeleton - genetics; Female; Fibroblasts - metabolism; Flagella - metabolism; Hedgehog Proteins; Humanities and Social Sciences; Humans; Male; multidisciplinary; Mutation; Pedigree; Science; Science (multidisciplinary); Short Rib-Polydactyly Syndrome - genetics
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms8092

The short rib polydactyly syndromes (SRPSs) are a heterogeneous group of autosomal recessive, perinatal lethal skeletal disorders characterized primarily by short, horizontal ribs, short limbs and polydactyly. Mutations in several genes affecting intraflagellar transport (IFT) cause SRPS but they do not account for all cases. Here we identify an additional SRPS gene and further unravel the functional basis for IFT. We perform whole-exome sequencing and identify mutations in a new disease-producing gene, cytoplasmic dynein-2 light intermediate chain 1, DYNC2LI1 , segregating with disease in three families. Using primary fibroblasts, we show that DYNC2LI1 is essential for dynein-2 complex stability and that mutations in DYNC2LI1 result in variable length, including hyperelongated, cilia, Hedgehog pathway impairment and ciliary IFT accumulations. The findings in this study expand our understanding of SRPS locus heterogeneity and demonstrate the importance of DYNC2LI1 in dynein-2 complex stability, cilium function, Hedgehog regulation and skeletogenesis. Mutations in genes affecting intraflagellar transport account for some but not all cases of short rib polydactyly syndromes. Here Taylor et al . use whole exome sequencing and in vivo cell line assays to identify novel disease associated mutations in DYNC2LI1 .