The homozygous variant c.797G>A/p.(Cys266Tyr) inPISDis associated with a Spondyloepimetaphyseal dysplasia with large epiphyses and disturbed mitochondrial function

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Abstract
Spondyloepimetaphyseal dysplasias (SEMD) are a group of genetically heterogeneous skeletal disorders characterized by abnormal vertebral bodies and epimetaphyseal abnormalities. We investigated two families with a new SEMD type with one proband each. They showed mild facial dysmorphism, flat vertebral bodies (platyspondyly), large epiphyses, metaphyseal dysplasia, and hallux valgus as common clinical features. By trio‐exome sequencing, the homozygous missense variant c.797G>A p.(Cys266Tyr) in PISD was found in both affected individuals. Based on exome data analyses for homozygous regions, the two patients shared a single homozygous block on chromosome 22 including PISD, indicating their remote consanguinity. PISD encodes phosphatidylserine decarboxylase that is localized in the inner mitochondrial membrane and catalyzes the decarboxylation of phosphatidylserine to phosphatidylethanolamine (PE) in mammalian cells. PE occurs at high abundance in mitochondrial membranes. Patient‐derived fibroblasts showed fragmented mitochondrial morphology. Treatment of patient cells with MG‐132 or staurosporine to induce activation of the intrinsic apoptosis pathway revealed significantly decreased cell viability with increased caspase‐3 and ‐7 activation. Remarkably, ethanolamine supplementation largely restored cell viability and enhanced apoptosis in MG‐132‐stressed patient cells. Our data demonstrate that the bi‐allelic hypomorphic PISD variant p.(Cys266Tyr) is associated with a novel SEMD form, which may be treatable with ethanolamine administration. This article is protected by copyright. All rights reserved
Funding Information
  • Deutsche Forschungsgemeinschaft (KU 1240/6-2)
  • Science and Engineering Research Board, The Department of Science and Technology, Government of India (SB/SO/HS/005/2014)

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