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BACKGROUND: Bone dysplasias are a large group of disorders affecting the growth and structure of the skeletal system. METHODS: In the present study, we report the clinical and molecular delineation of a new form of syndromic autosomal recessive spondylometaphyseal dysplasia (SMD) in two Emirati first cousins. They displayed postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, radiological abnormalities involving the spine, pelvis and metaphyses, corneal clouding and intellectual disability. Whole genome homozygosity mapping localised the genetic cause to 11q12.1-q13.1, a region spanning 19.32 Mb with ~490 genes. Using whole exome sequencing, we identified four novel homozygous variants within the shared block of homozygosity. Pathogenic variants in genes involved in phospholipid metabolism, such as PLCB4 and PCYT1A, are known to cause bone dysplasia with or without eye anomalies, which led us to select PLCB3 as a strong candidate. This gene encodes phospholipase C β 3, an enzyme that converts phosphatidylinositol 4,5 bisphosphate (PIP2) to inositol 1,4,5 triphosphate (IP3) and diacylglycerol. RESULTS: The identified variant (c.2632G>T) substitutes a serine for a highly conserved alanine within the Ha2' element of the proximal C-terminal domain. This disrupts binding of the Ha2' element to the catalytic core and destabilises PLCB3. Here we show that this hypomorphic variant leads to elevated levels of PIP2 in patient fibroblasts, causing disorganisation of the F-actin cytoskeleton. CONCLUSIONS: Our results connect a homozygous loss of function variant in PLCB3 with a new SMD associated with corneal dystrophy and developmental delay (SMDCD).

Original publication

DOI

10.1136/jmedgenet-2017-104827

Type

Journal article

Journal

J Med Genet

Publication Date

02/2018

Volume

55

Pages

122 - 130

Keywords

disorganization of actin cytoskeletal network, hypomorphic variant, pip2 accumulation, plcb3, spondylometaphyseal dysplasia with corneal dystrophy (smdcd), Amino Acid Substitution, Child, Child, Preschool, Chromosomes, Human, Pair 11, Corneal Dystrophies, Hereditary, Developmental Disabilities, Female, Homozygote, Humans, Infant, Newborn, Intellectual Disability, Male, Osteochondrodysplasias, Pedigree, Phosphatidylinositols, Phospholipase C beta, Signal Transduction