Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment

Myriam Srour, Véronique Caron, Toni Pearson, Sarah B. Nielsen, Sébastien Lévesque, Marie Ange Delrue, Troy A. Becker, Fadi F. Hamdan, Zoha Kibar, Shannon G. Sattler, Michael C. Schneider, Pierre Bitoun, Nicolas Chassaing, Jill A. Rosenfeld, Fan Xia, Sonal Desai, Elizabeth Roeder, Virginia Kimonis, Adele Schneider, Rebecca Okashah LittlejohnSofia Douzgou, André Tremblay, Jacques L. Michaud

Research output: Contribution to journalArticle

19 Scopus citations

Abstract

Retinoic acid (RA) signaling plays a key role in the development and function of several systems in mammals. We previously discovered that the de novo mutations c.1159C>T (p.Arg387Cys) and c.1159C>A (p.Arg387Ser) in the RA Receptor Beta (RARB) gene cause microphthalmia and diaphragmatic hernia. However, the natural history of affected subjects beyond the prenatal or neonatal period was unknown. Here, we describe nine additional subjects with microphthalmia who have de novo mutations in RARB, including the previously described p.Arg387Cys as well as the novel c.887G>C (p.Gly296Ala) and c.638T>C (p.Leu213Pro). Moreover, we review the information on four previously reported cases. All subjects who survived the neonatal period (n = 10) displayed severe global developmental delay with progressive motor impairment due to spasticity and/or dystonia (with or without chorea). The majority of subjects also showed Chiari type I malformation and severe feeding difficulties. We previously found that p.Arg387Cys and p.Arg387Ser induce a gain-of-function. We show here that the p.Gly296Ala and p.Leu213Pro RARB mutations further promote the RA ligand-induced transcriptional activity by twofold to threefold over the wild-type receptor, also indicating a gain-of-function mechanism. These observations suggest that precise regulation of RA signaling is required for brain development and/or function in humans.

Original languageEnglish
Pages (from-to)786-793
Number of pages8
JournalHuman mutation
Volume37
Issue number8
DOIs
StatePublished - Aug 1 2016
Externally publishedYes

Keywords

  • RARB
  • developmental delay
  • gain-of-function
  • intellectual disability
  • movement disorder
  • retinoic acid

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    Srour, M., Caron, V., Pearson, T., Nielsen, S. B., Lévesque, S., Delrue, M. A., Becker, T. A., Hamdan, F. F., Kibar, Z., Sattler, S. G., Schneider, M. C., Bitoun, P., Chassaing, N., Rosenfeld, J. A., Xia, F., Desai, S., Roeder, E., Kimonis, V., Schneider, A., ... Michaud, J. L. (2016). Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment. Human mutation, 37(8), 786-793. https://doi.org/10.1002/humu.23004