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Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.

Publication ,  Journal Article
Wetzel-Strong, SE; Galeffi, F; Benavides, C; Patrucco, M; Bullock, JL; Gallione, CJ; Lee, HK; Marchuk, DA
Published in: Genetics
August 9, 2023

Sturge-Weber Syndrome (SWS) is a sporadic (non-inherited) syndrome characterized by capillary vascular malformations in the facial skin, leptomeninges, or the choroid. A hallmark feature is the mosaic nature of the phenotype. SWS is caused by a somatic mosaic mutation in the GNAQ gene (p.R183Q), leading to activation of the G protein, Gαq. Decades ago, Rudolf Happle hypothesized SWS as an example of "paradominant inheritance", that is, a "lethal gene (mutation) surviving by mosaicism". He predicted that the "presence of the mutation in the zygote will lead to death of the embryo at an early stage of development". We have created a mouse model for SWS using gene targeting to conditionally express the GNAQ p.R183Q mutation. We have employed two different Cre-drivers to examine the phenotypic effects of expression of this mutation at different levels and stages of development. As predicted by Happle, global, ubiquitous expression of this mutation in the blastocyst stage results in 100% embryonic death. The majority of these developing embryos show vascular defects consistent with the human vascular phenotype. By contrast, global but mosaic expression of the mutation enables a fraction of the embryos to survive, but those that survive to birth and beyond do not exhibit obvious vascular defects. These data validate Happle's paradominant inheritance hypothesis for SWS and suggest the requirement of a tight temporal and developmental window of mutation expression for the generation of the vascular phenotype. Furthermore, these engineered murine alleles provide the template for the development of a mouse model of SWS that acquires the somatic mutation during embryonic development, but permits the embryo to progress to live birth and beyond, so that postnatal phenotypes can also be investigated. These mice could then also be employed in pre-clinical studies of novel therapies.

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Published In

Genetics

DOI

EISSN

1943-2631

Publication Date

August 9, 2023

Volume

224

Issue

4

Location

United States

Related Subject Headings

  • Vascular Malformations
  • Sturge-Weber Syndrome
  • Mutation
  • Mice
  • Male
  • Humans
  • Developmental Biology
  • Capillaries
  • Animals
  • 3105 Genetics
 

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Wetzel-Strong, S. E., Galeffi, F., Benavides, C., Patrucco, M., Bullock, J. L., Gallione, C. J., … Marchuk, D. A. (2023). Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis. Genetics, 224(4). https://doi.org/10.1093/genetics/iyad077
Wetzel-Strong, Sarah E., Francesca Galeffi, Christian Benavides, Mary Patrucco, Jessica L. Bullock, Carol J. Gallione, Han Kyu Lee, and Douglas A. Marchuk. “Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.Genetics 224, no. 4 (August 9, 2023). https://doi.org/10.1093/genetics/iyad077.
Wetzel-Strong SE, Galeffi F, Benavides C, Patrucco M, Bullock JL, Gallione CJ, et al. Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis. Genetics. 2023 Aug 9;224(4).
Wetzel-Strong, Sarah E., et al. “Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.Genetics, vol. 224, no. 4, Aug. 2023. Pubmed, doi:10.1093/genetics/iyad077.
Wetzel-Strong SE, Galeffi F, Benavides C, Patrucco M, Bullock JL, Gallione CJ, Lee HK, Marchuk DA. Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis. Genetics. 2023 Aug 9;224(4).

Published In

Genetics

DOI

EISSN

1943-2631

Publication Date

August 9, 2023

Volume

224

Issue

4

Location

United States

Related Subject Headings

  • Vascular Malformations
  • Sturge-Weber Syndrome
  • Mutation
  • Mice
  • Male
  • Humans
  • Developmental Biology
  • Capillaries
  • Animals
  • 3105 Genetics