Abstract
BackgroundThe family of Fragile X Mental Retardation Proteins is composed of three members: Fragile Mental Retardation 1, Fragile X Related 1 and X Related 2 proteins. These proteins are associated with mRNPs within translating ribosomes and have the capacity to shuttle between the nucleus and the cytoplasm. Great attention has been given to FMRP due to its implication in human hereditary mental retardation while FXR1P and FXR2P have only recently been studied.ResultsUsing antibodies directed against several epitopes of FXR1P, we have detected protein isoforms generated by small peptides pocket inserts. Four isoforms of MW 70, 74, 78, 80 kDa are widely distributed in mouse organs, while in striated muscles these isoforms are replaced by proteins of 82 and 84 kDa containing an extra pocket of 27 aa. Expression of these muscle isoforms is an early event during in vitro differentiation of myoblasts into myotubes and correlates with the activation of muscle-specific genes. However, while FXR1P82,84 are associated with cytoplasmic mRNPs in myotubes, they are sequestered in the nuclei of undifferentiated myoblasts. These observations suggest that, in addition to a cytoplasmic function yet to be defined, FXR1P82,84 may play a nuclear role in pre-mRNA metabolism.ConclusionsThe pattern of subcellular partitioning of FXR1P isoforms during myogenesis is unique among the family of the FXR proteins. The model system described here should be considered as a powerful tool for ongoing attempts to unravel structure-function relationships of the different FMR family members since the potential role(s) of FXR1P as a compensatory factor in Fragile X syndrome is still elusive.
Highlights
The family of Fragile X Mental Retardation Proteins is composed of three members: Fragile Mental Retardation 1, Fragile X Related 1 and X Related 2 proteins
The additionnal band detected at 94 kDa with mAb3FX corresponds to the closely homologous Fragile X Related 2 protein [5] recognized by this monoclonal antibody since part of the peptide used for immunization is present in FXR2P
We propose that FXR1P82,84 might be sequestered in nucleoplasmic complexes in undifferentiated myoblasts and once cells are committed to differentiate, P82,84 are transferred to the cytoplasm with messenger RiboNucleoParticles http://www.biomedcentral.com/1471-2156/1/4 (mRNP) carrying the newly processed mRNAs specific to the differentiated stage of myotubes
Summary
The family of Fragile X Mental Retardation Proteins is composed of three members: Fragile Mental Retardation 1, Fragile X Related 1 and X Related 2 proteins. The Fragile X Mental Retardation Protein (FMRP) is coded by the X-linked FMR1 gene and its absence is directly associated with human hereditary mental retardation [reviewed in 1,2]. Two other members of this family are the Fragile X Related 1 (FXR1P) and Fragile X Related 2 (FXR2P) proteins [3,4,5] that are coded by the FXR1 and FXR2 genes located at 3q28 and 17p13.1, respectively, in human These genes are highly conserved in vertebrate evolution and contain two KH domains and a RGG box that are functional characteristic motifs in RNA-binding proteins [4,5,6,7]. FMRP as well as the other members of the family have been shown to be associated with messenger RiboNucleoParticles http://www.biomedcentral.com/1471-2156/1/4
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