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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.

Oguz Kanca | Jonathan C Andrews | Pei-Tseng Lee | Chirag Patel | Stephen R Braddock | Anne M Slavotinek | Julie S Cohen | Cynthia S Gubbels | Kimberly A Aldinger | Judy Williams | Maanasa Indaram | Ali Fatemi | Timothy W Yu | Pankaj B Agrawal | Gilbert Vezina | Cas Simons | Joanna Crawford | C Christopher Lau | Undiagnosed Diseases Network | Wendy K Chung | Thomas C Markello | William B Dobyns | David R Adams | William A Gahl | Michael F Wangler | Shinya Yamamoto | Hugo J Bellen | May Christine V Malicdan
American journal of human genetics | 2019

WD40 repeat-containing proteins form a large family of proteins present in all eukaryotes. Here, we identified five pediatric probands with de novo variants in WDR37, which encodes a member of the WD40 repeat protein family. Two probands shared one variant and the others have variants in nearby amino acids outside the WD40 repeats. The probands exhibited shared phenotypes of epilepsy, colobomas, facial dysmorphology reminiscent of CHARGE syndrome, developmental delay and intellectual disability, and cerebellar hypoplasia. The WDR37 protein is highly conserved in vertebrate and invertebrate model organisms and is currently not associated with a human disease. We generated a null allele of the single Drosophila ortholog to gain functional insights and replaced the coding region of the fly gene CG12333/wdr37 with GAL4. These flies are homozygous viable but display severe bang sensitivity, a phenotype associated with seizures in flies. Additionally, the mutant flies fall when climbing the walls of the vials, suggesting a defect in grip strength, and repeat the cycle of climbing and falling. Similar to wall clinging defect, mutant males often lose grip of the female abdomen during copulation. These phenotypes are rescued by using the GAL4 in the CG12333/wdr37 locus to drive the UAS-human reference WDR37 cDNA. The two variants found in three human subjects failed to rescue these phenotypes, suggesting that these alleles severely affect the function of this protein. Taken together, our data suggest that variants in WDR37 underlie a novel syndromic neurological disorder.

Pubmed ID: 31327508

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Associated grants

  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001863
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS050375
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM067858
  • Agency: Wellcome Trust, United Kingdom
  • Agency: NINDS NIH HHS, United States
    Id: F32 NS110174
  • Agency: NINDS NIH HHS, United States
    Id: U54 NS093793
  • Agency: NIH HHS, United States
    Id: R24 OD022005

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Bloomington Drosophila Stock Center (biomaterial supply resource)

RRID:SCR_006457

Collects, maintains and distributes Drosophila melanogaster strains for research. Emphasis is placed on genetic tools that are useful to a broad range of investigations. These include basic stocks of flies used in genetic analysis such as marker, balancer, mapping, and transposon-tagging strains; mutant alleles of identified genes, including a large set of transposable element insertion alleles; defined sets of deficiencies and a variety of other chromosomal aberrations; engineered lines for somatic and germline clonal analysis; GAL4 and UAS lines for targeted gene expression; enhancer trap and lacZ-reporter strains with defined expression patterns for marking tissues; and a collection of transposon-induced lethal mutations.

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