NUFIP1 (Nuclear FMRP Interacting Protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes
Experimental Cell Research: emphasizing molecular approaches to cell biology , Volume 289 - Issue 1 p. 95- 107
Fragile X syndrome, the most common cause of inherited mental retardation, is caused by the absence of FMRP (Fragile X Mental Retardation Protein). FMRP is an RNA binding protein reported to be involved in translational control, notably at postsynaptic sites of protein synthesis as a part of a multiprotein/mRNA complex. One of the FMRP interactors, NUFIP1, is an RNA binding protein with an expression profile matching that of FMRP. We now show that in the nucleus NUFIP1 is localized in the nuclear matrix in RNA-containing structures lying in the proximity of, but not overlapping with, sites of nascent RNA. NUFIP1 is also present in the cytoplasm, where it is associated with ribosomes, similarly to FMRP. In neurons NUFIP1 can be detected in functional synaptoneurosomes, colocalizing with ribosomes. Consistent with its subcellular localization in both nucleus and cytoplasm, we show that NUFIP1 contains a functional CRM1-dependent nuclear export signal and is able to shuttle between these two cellular compartments. These findings suggest the involvement of NUFIP1 in the export and localization of mRNA and, in association with FMRP, in the regulation of local protein synthesis near synapses.
|Fragile-X syndrome, Mental retardation, Nuclear export signal (NES), Nuclear matrix, RNA binding protein, Synaptoneurosomes|
|Experimental Cell Research: emphasizing molecular approaches to cell biology|
|Organisation||Department of Clinical Genetics|
Bardoni, B, Willemsen, R, Weiler, J.M, Schenck, A, Severijnen, E.A.W.F.M, Hindelang, C, … Mandel, J.-L. (2003). NUFIP1 (Nuclear FMRP Interacting Protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes. Experimental Cell Research: emphasizing molecular approaches to cell biology, 289(1), 95–107. doi:10.1016/S0014-4827(03)00222-2