Sumoylation regulates FMRP-mediated dendritic spine elimination and maturation
Fragile X syndrome patients display intellectual disability and autism, caused by mutations in the RNA-binding protein fragile X mental retardation protein (FMRP). Here, the authors show that FMRP sumoylation is required for regulating spine density and maturation.
Saved in:
Main Authors: | Anouar Khayachi, Carole Gwizdek, Gwénola Poupon, Damien Alcor, Magda Chafai, Frédéric Cassé, Thomas Maurin, Marta Prieto, Alessandra Folci, Fabienne De Graeve, Sara Castagnola, Romain Gautier, Lenka Schorova, Céline Loriol, Marie Pronot, Florence Besse, Frédéric Brau, Emmanuel Deval, Barbara Bardoni, Stéphane Martin |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2018
|
Subjects: | |
Online Access: | https://doaj.org/article/57e3d66daa9b4a92b4183ee79455e739 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice
by: Marta Prieto, et al.
Published: (2021) -
Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
by: Marie Pronot, et al.
Published: (2021) -
Altered inflammatory response in FMRP-deficient microglia
by: Jennifer M. Parrott, et al.
Published: (2021) -
FMRP regulates an ethanol-dependent shift in GABABR function and expression with rapid antidepressant properties
by: Sarah A. Wolfe, et al.
Published: (2016) -
Uncovering the SUMOylation and ubiquitylation crosstalk in human cells using sequential peptide immunopurification
by: Frédéric Lamoliatte, et al.
Published: (2017)