RGD Reference Report - Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy. - Rat Genome Database

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Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.

Authors: Riazuddin, SA  Parker, DS  McGlumphy, EJ  Oh, EC  Iliff, BW  Schmedt, T  Jurkunas, U  Schleif, R  Katsanis, N  Gottsch, JD 
Citation: Riazuddin SA, etal., Am J Hum Genet. 2012 Mar 9;90(3):533-9. doi: 10.1016/j.ajhg.2012.01.013. Epub 2012 Feb 16.
RGD ID: 11072687
Pubmed: PMID:22341973   (View Abstract at PubMed)
PMCID: PMC3309196   (View Article at PubMed Central)
DOI: DOI:10.1016/j.ajhg.2012.01.013   (Journal Full-text)

Fuchs corneal dystrophy (FCD) is a genetic disorder of the corneal endothelium and is the most common cause of corneal transplantation in the United States. Previously, we mapped a late-onset FCD locus, FCD2, on chromosome 18q. Here, we present next-generation sequencing of all coding exons in the FCD2 critical interval in a multigenerational pedigree in which FCD segregates as an autosomal-dominant trait. We identified a missense change in LOXHD1, a gene causing progressive hearing loss in humans, as the sole variant capable of explaining the phenotype in this pedigree. We observed LOXHD1 mRNA in cultured human corneal endothelial cells, whereas antibody staining of both human and mouse corneas showed staining in the corneal epithelium and endothelium. Corneal sections of the original proband were stained for LOXHD1 and demonstrated a distinct increase in antibody punctate staining in the endothelium and Descemet membrane; punctate staining was absent from both normal corneas and FCD corneas negative for causal LOXHD1 mutations. Subsequent interrogation of a cohort of >200 sporadic affected individuals identified another 15 heterozygous missense mutations that were absent from >800 control chromosomes. Furthermore, in silico analyses predicted that these mutations reside on the surface of the protein and are likely to affect the protein's interface and protein-protein interactions. Finally, expression of the familial LOXHD1 mutant allele as well as two sporadic mutations in cells revealed prominent cytoplasmic aggregates reminiscent of the corneal phenotype. All together, our data implicate rare alleles in LOXHD1 in the pathogenesis of FCD and highlight how different mutations in the same locus can potentially produce diverse phenotypes.

Disease Annotations    

Objects Annotated

Genes (Rattus norvegicus)
Loxhd1  (lipoxygenase homology PLAT domains 1)

Genes (Mus musculus)
Loxhd1  (lipoxygenase homology domains 1)

Genes (Homo sapiens)
LOXHD1  (lipoxygenase homology PLAT domains 1)

Additional Information