From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome.

Details

Serval ID
serval:BIB_F6BA6B08DA7D
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Title
From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome.
Journal
Nature reviews. Neuroscience
Author(s)
Bagni C., Greenough W.T.
ISSN
1471-003X (Print)
ISSN-L
1471-003X
Publication state
Published
Issued date
05/2005
Volume
6
Number
5
Pages
376-387
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S. ; Review
Publication Status: ppublish
Abstract
The mental retardation protein FMRP is involved in the transport of mRNAs and their translation at synapses. Patients with fragile X syndrome, in whom FMRP is absent or mutated, show deficits in learning and memory that might reflect impairments in the translational regulation of a subset of neuronal mRNAs. The study of FMRP provides important insights into the regulation and functions of local protein synthesis in the neuronal periphery, and increases our understanding of how these functions can produce specific effects at individual synapses.

Keywords
Animals, Fragile X Mental Retardation Protein, Fragile X Syndrome/genetics, Fragile X Syndrome/metabolism, Fragile X Syndrome/pathology, Humans, Nerve Tissue Proteins/deficiency, Nerve Tissue Proteins/genetics, Nerve Tissue Proteins/physiology, Protein Transport/genetics, RNA-Binding Proteins/genetics, RNA-Binding Proteins/physiology, Ribonucleoproteins/genetics, Ribonucleoproteins/metabolism, Spinal Cord/abnormalities, Spinal Cord/metabolism
Pubmed
Create date
06/03/2017 17:23
Last modification date
20/08/2019 16:23
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