Twenty years of SynGAP research: from synapses to cognition

TR Gamache, Y Araki, RL Huganir - Journal of Neuroscience, 2020 - Soc Neuroscience
SynGAP is a potent regulator of biochemical signaling in neurons and plays critical roles in
neuronal function. It was first identified in 1998, and has since been extensively …

Emerging roles of O-glycosylation in regulating protein aggregation, phase separation, and functions

X Li, Y Du, X Chen, C Liu - Current Opinion in Chemical Biology, 2023 - Elsevier
Protein O-glycosylation is widely identified in various proteins involved in diverse biological
processes. Recent studies have demonstrated that O-glycosylation plays crucial and …

O-GlcNAcylation modulates liquid–liquid phase separation of SynGAP/PSD-95

P Lv, Y Du, C He, L Peng, X Zhou, Y Wan, M Zeng… - Nature Chemistry, 2022 - nature.com
Liquid–liquid phase separation (LLPS) of SynGAP and PSD-95, two abundant proteins that
interact in the postsynaptic density (PSD) of neurons, has been implicated in modulating …

Rapid dispersion of SynGAP from synaptic spines triggers AMPA receptor insertion and spine enlargement during LTP

Y Araki, M Zeng, M Zhang, RL Huganir - Neuron, 2015 - cell.com
Summary SynGAP is a Ras-GTPase activating protein highly enriched at excitatory
synapses in the brain. Previous studies have shown that CaMKII and the RAS-ERK pathway …

Differential roles of NR2A-and NR2B-containing NMDA receptors in Ras-ERK signaling and AMPA receptor trafficking

MJ Kim, AW Dunah, YT Wang, M Sheng - Neuron, 2005 - cell.com
NMDA receptors (NMDARs) control bidirectional synaptic plasticity by regulating
postsynaptic AMPA receptors (AMPARs). Here we show that NMDAR activation can have …

Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

MH Berryer, FF Hamdan, LL Klitten, RS Møller… - Human …, 2013 - Wiley Online Library
De novo mutations in SYNGAP1, which codes for a RAS/RAP GTP‐activating protein, cause
nonsyndromic intellectual disability (NSID). All disease‐causing point mutations identified …

[HTML][HTML] Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation

FF Hamdan, J Gauthier, D Spiegelman… - … England Journal of …, 2009 - Mass Medical Soc
Although autosomal forms of nonsyndromic mental retardation account for the majority of
cases of mental retardation, the genes that are involved remain largely unknown. We …

SynGAP-MUPP1-CaMKII synaptic complexes regulate p38 MAP kinase activity and NMDA receptor-dependent synaptic AMPA receptor potentiation

G Krapivinsky, I Medina, L Krapivinsky, S Gapon… - Neuron, 2004 - cell.com
The synapse contains densely localized and interacting proteins that enable it to adapt to
changing inputs. We describe a Ca 2+-sensitive protein complex involved in the regulation …

De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism

FF Hamdan, H Daoud, A Piton, J Gauthier… - Biological …, 2011 - Elsevier
BACKGROUND: Little is known about the genetics of nonsyndromic intellectual disability
(NSID). Recently, we reported de novo truncating mutations in the SYNGAP1 gene of 3 of 94 …

The role of synaptic GTPase-activating protein in neuronal development and synaptic plasticity

JH Kim, HK Lee, K Takamiya… - Journal of …, 2003 - Soc Neuroscience
Synaptic GTPase-activating protein (SynGAP) is a neuronal RasGAP (Ras GTPase-
activating protein) that is selectively expressed in brain and highly enriched at excitatory …