Fragile X Mental Retardation Protein: Past, Present and Future

Author(s): Miri Kim, Stephanie Ceman.

Journal Name: Current Protein & Peptide Science

Volume 13 , Issue 4 , 2012

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Abstract:

We begin by reviewing the first characterization of fragile X syndrome, which ultimately led to cloning of the FMR1 gene. Discovery of the molecular basis of this disorder, including expansion of a trinucleotide repeat, gave insight not only into fragile X syndrome but also into the premutation syndromes. Features of fragile X syndrome are discussed including the patient phenotype down to the neuronal phenotype. The domain features of the fragile X mental retardation protein FMRP are described, as are the mRNAs bound by FMRP and the role of post-translational modifications as regulators of FMRP function. The relatively new role of FMRP in progenitor cells is reviewed, as is FMRP localization in cells and how FMRP is regulated by glutamatergic signaling in the brain. Understanding how metabotropic glutamate receptors impact FMRP has led to novel therapeutic approaches in treating this disorder.

Keywords: Fragile X, FMRP, RNA binding protein, posttranslational modification, trinucleotide repeat disorder, translation regulation, Fragile X Syndrome, FXS, CGG, FMR1 coding sequence.

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Article Details

VOLUME: 13
ISSUE: 4
Year: 2012
Page: [358 - 371]
Pages: 14
DOI: 10.2174/138920312801619420
Price: $58

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