SUMOylation is a dynamic post-translational modification that consists in the covalent but reversible enzymatic conjugation of the Small Ubiquitin-like MOdifier (SUMO) protein on specific lysine residues of target proteins. In the last 10 years, SUMOylation has emerged as an important regulator of the neuronal function, playing a role in brain...
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September 23, 2021 (v1)PublicationUploaded on: October 11, 2023
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June 2022 (v1)Journal article
International audience
Uploaded on: December 4, 2022 -
November 23, 2021 (v1)Journal article
Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and functional changes. Many molecular processes are involved in this regulation, including...
Uploaded on: December 3, 2022 -
November 23, 2021 (v1)Journal article
Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and functional changes. Many molecular processes are involved in this regulation, including...
Uploaded on: February 22, 2023 -
August 2019 (v1)Journal article
Sumoylation is a reversible post-translational modification essential to the modulation of neuronal function, including neurotransmitter release and synaptic plasticity. A tightly regulated equilibrium between the sumoylation and desumoylation processes is critical to the brain function and its disruption has been associated with several...
Uploaded on: December 4, 2022 -
September 27, 2022 (v1)Journal article
Fragile X-Syndrome (FXS) represents the most common inherited form of intellectual disability and the leading monogenic cause of Autism Spectrum Disorders. In most cases, this disease results from the absence of expression of the protein FMRP encoded by the FMR1 gene (Fragile X messenger ribonucleoprotein 1). FMRP is mainly defined as a...
Uploaded on: December 4, 2022 -
July 2022 (v1)Journal article
SUMOylation is a post-translational modification essential to cell homeostasis. A tightly controlled equilibrium between SUMOylation and deSUMOylation processes is also critical to the neuronal function including neurotransmitter release and synaptic transmission and plasticity. Disruption of the SUMOylation homeostasis in neurons is associated...
Uploaded on: December 3, 2022 -
December 26, 2020 (v1)Publication
Dopamine transmission is a monoaminergic system involved in reward processing and motor control. Volume transmission is thought to be the main mechanism by which monoamines modulate effector transmission though synaptic structures are scarcely described. Here, we applied a fluorescence activated synaptosome sorting workflow to dopaminergic...
Uploaded on: June 20, 2023 -
November 19, 2021 (v1)Publication
Dopamine is a monoamine involved in reward processing and motor control. Volume transmission is thought to be the mechanism by which monoamines modulate effector systems at glutamate and GABA synapses. Hence, dopamine synapses are scarcely described. We applied fluorescence activated synaptosome sorting to explore the features of the...
Uploaded on: December 4, 2022 -
February 22, 2018 (v1)Journal article
Fragile X syndrome (FXS) is the most frequent inherited cause of intellectual disability and the best-studied monogenic cause of autism. FXS results from the functional absence of the fragile X mental retardation protein (FMRP) leading to abnormal pruning and consequently to synaptic communication defects. Here we show that FMRP is a substrate...
Uploaded on: December 4, 2022 -
December 2018 (v1)Journal article
International audience
Uploaded on: February 22, 2023 -
December 2018 (v1)Journal article
International audience
Uploaded on: December 4, 2022 -
December 2018 (v1)Journal article
International audience
Uploaded on: February 22, 2023 -
December 14, 2020 (v1)Publication
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. FXS is usually caused by a CGG-repeat expansion in the FMR1 gene leading to its silencing and the loss-of-expression of the Fragile X Mental Retardation Protein (FMRP). Missense mutations were also identified...
Uploaded on: December 4, 2022 -
December 2018 (v1)Journal article
International audience
Uploaded on: December 4, 2022 -
March 10, 2021 (v1)Journal article
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. CGG-repeat expansion in the FMR1 gene leads to FMR1 silencing, loss-of-expression of the Fragile X Mental Retardation Protein (FMRP), and is a common cause of FXS. Missense mutations in the FMR1 gene were...
Uploaded on: December 4, 2022