Journal article
New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes
Abstract
Cytoplasmic FMRP interacting protein 1 (CYFIP1) is a candidate gene for intellectual disability (ID), autism, schizophrenia and epilepsy. It is a member of a family of proteins that is highly conserved during evolution, sharing high homology with its Drosophila homolog, dCYFIP. CYFIP1 interacts with the Fragile X mental retardation protein (FMRP, encoded by the FMR1 gene), whose absence causes Fragile X syndrome, and with the translation …
Authors
Abekhoukh S; Sahin HB; Grossi M; Zongaro S; Maurin T; Madrigal I; Kazue-Sugioka D; Raas-Rothschild A; Doulazmi M; Carrera P
Journal
Disease Models & Mechanisms, Vol. 10, No. 4, pp. 463–474
Publisher
The Company of Biologists
Publication Date
April 1, 2017
DOI
10.1242/dmm.025809
ISSN
1754-8403
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Adaptor Proteins, Signal TransducingAnimalsCells, CulturedDrosophila ProteinsDrosophila melanogasterEpistasis, GeneticFragile X Mental Retardation ProteinGene Knockout TechniquesGene SilencingHumansMice, Inbred C57BLMultiprotein ComplexesNerve Tissue ProteinsNeuronsOlfactory BulbRNA, MessengerWiskott-Aldrich Syndrome Protein Family