Dataset Information

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.

ABSTRACT: Variants in RAC3, encoding a small GTPase RAC3 which is critical for the regulation of actin cytoskeleton and intracellular signal transduction, are associated with a rare neurodevelopmental disorder with structural brain anomalies and facial dysmorphism. We investigated a cohort of 10 unrelated participants presenting with global psychomotor delay, hypotonia, behavioural disturbances, stereotyped movements, dysmorphic features, seizures and musculoskeletal abnormalities. MRI of brain revealed a complex pattern of variable brain malformations, including callosal abnormalities, white matter thinning, grey matter heterotopia, polymicrogyria/dysgyria, brainstem anomalies and cerebellar dysplasia. These patients harboured eight distinct de novo RAC3 variants, including six novel variants (NM_005052.3): c.34G > C p.G12R, c.179G > A p.G60D, c.186_188delGGA p.E62del, c.187G > A p.D63N, c.191A > G p.Y64C and c.348G > C p.K116N. We then examined the pathophysiological significance of these novel and previously reported pathogenic variants p.P29L, p.P34R, p.A59G, p.Q61L and p.E62K. In vitro analyses revealed that all tested RAC3 variants were biochemically and biologically active to variable extent, and exhibited a spectrum of different affinities to downstream effectors including p21-activated kinase 1. We then focused on the four variants p.Q61L, p.E62del, p.D63N and p.Y64C in the Switch II region, which is essential for the biochemical activity of small GTPases and also a variation hot spot common to other Rho family genes, RAC1 and CDC42. Acute expression of the four variants in embryonic mouse brain using in utero electroporation caused defects in cortical neuron morphology and migration ending up with cluster formation during corticogenesis. Notably, defective migration by p.E62del, p.D63N and p.Y64C were rescued by a dominant negative version of p21-activated kinase 1. Our results indicate that RAC3 variants result in morphological and functional defects in cortical neurons during brain development through variant-specific mechanisms, eventually leading to heterogeneous neurodevelopmental phenotypes.

SUBMITTER: Scala M

PROVIDER: S-EPMC9473360 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.

Scala Marcello M Nishikawa Masashi M Ito Hidenori H Tabata Hidenori H Khan Tayyaba T Accogli Andrea A Davids Laura L Ruiz Anna A Chiurazzi Pietro P Cericola Gabriella G Schulte Björn B Monaghan Kristin G KG Begtrup Amber A Torella Annalaura A Pinelli Michele M Denommé-Pichon Anne Sophie AS Vitobello Antonio A Racine Caroline C Mancardi Maria Margherita MM Kiss Courtney C Guerin Andrea A Wu Wendy W Gabau Vila Elisabeth E Mak Bryan C BC Martinez-Agosto Julian A JA Gorin Michael B MB Duz Bugrahan B Bayram Yavuz Y Carvalho Claudia M B CMB Vengoechea Jaime E JE Chitayat David D Tan Tiong Yang TY Callewaert Bert B Kruse Bernd B Bird Lynne M LM Faivre Laurence L Zollino Marcella M Biskup Saskia S Striano Pasquale P Nigro Vincenzo V Severino Mariasavina M Capra Valeria V Costain Gregory G Nagata Koh Ichi KI

Brain : a journal of neurology 20220901 9

Variants in RAC3, encoding a small GTPase RAC3 which is critical for the regulation of actin cytoskeleton and intracellular signal transduction, are associated with a rare neurodevelopmental disorder with structural brain anomalies and facial dysmorphism. We investigated a cohort of 10 unrelated participants presenting with global psychomotor delay, hypotonia, behavioural disturbances, stereotyped movements, dysmorphic features, seizures and musculoskeletal abnormalities. MRI of brain revealed a ...[more]

PMID: 35851598

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Dataset Information

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.

Publications

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.

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