SnapShot: FMRP interacting proteins

Emanuela Pasciuto; Claudia Bagni

doi:10.1016/j.cell.2014.08.036

SnapShot: FMRP interacting proteins

Cell. 2014 Sep 25;159(1):218-218.e1. doi: 10.1016/j.cell.2014.08.036.

Authors

Emanuela Pasciuto¹, Claudia Bagni²

Affiliations

¹ VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium.
² VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium; Department of Biomedicine and Prevention, University of Rome "Tor Vergata," 00133 Rome, Italy.

PMID: 25259928
DOI: 10.1016/j.cell.2014.08.036

Abstract

The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.

MeSH terms

Animals
Fragile X Mental Retardation Protein / metabolism*
Fragile X Syndrome / metabolism
Humans
Protein Interaction Maps
RNA, Messenger / metabolism

Substances

RNA, Messenger
Fragile X Mental Retardation Protein