Literature DB >> 32878499

Fragile X-related protein family: a double-edged sword in neurodevelopmental disorders and cancer.

Mrinmoyee Majumder1, Roger H Johnson2, Viswanathan Palanisamy1.   

Abstract

The fragile X-related (FXR) family proteins FMRP, FXR1, and FXR2 are RNA binding proteins that play a critical role in RNA metabolism, neuronal plasticity, and muscle development. These proteins share significant homology in their protein domains, which are functionally and structurally similar to each other. FXR family members are known to play an essential role in causing fragile X mental retardation syndrome (FXS), the most common genetic form of autism spectrum disorder. Recent advances in our understanding of this family of proteins have occurred in tandem with discoveries of great importance to neurological disorders and cancer biology via the identification of their novel RNA and protein targets. Herein, we review the FXR family of proteins as they pertain to FXS, other mental illnesses, and cancer. We emphasize recent findings and analyses that suggest contrasting functions of this protein family in FXS and tumorigenesis based on their expression patterns in human tissues. Finally, we discuss current gaps in our knowledge regarding the FXR protein family and their role in FXS and cancer and suggest future studies to facilitate bench to bedside translation of the findings.

Entities:  

Keywords:  FMRP; FXR1; FXR2; RNA binding; cancer; fragile X mental retardation syndrome; post-transcriptional gene regulation; post-translational protein modification; protein domains

Mesh:

Substances:

Year:  2020        PMID: 32878499      PMCID: PMC7695039          DOI: 10.1080/10409238.2020.1810621

Source DB:  PubMed          Journal:  Crit Rev Biochem Mol Biol        ISSN: 1040-9238            Impact factor:   8.250


  127 in total

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4.  Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse.

Authors:  C E Bakker; Y de Diego Otero; C Bontekoe; P Raghoe; T Luteijn; A T Hoogeveen; B A Oostra; R Willemsen
Journal:  Exp Cell Res       Date:  2000-07-10       Impact factor: 3.905

Review 5.  The translation of translational control by FMRP: therapeutic targets for FXS.

Authors:  Jennifer C Darnell; Eric Klann
Journal:  Nat Neurosci       Date:  2013-04-14       Impact factor: 24.884

6.  Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome.

Authors:  H Siomi; M Choi; M C Siomi; R L Nussbaum; G Dreyfuss
Journal:  Cell       Date:  1994-04-08       Impact factor: 41.582

7.  The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction.

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Journal:  Structure       Date:  2006-01       Impact factor: 5.006

8.  CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.

Authors:  Silvia De Rubeis; Emanuela Pasciuto; Ka Wan Li; Esperanza Fernández; Daniele Di Marino; Andrea Buzzi; Linnaea E Ostroff; Eric Klann; Fried J T Zwartkruis; Noboru H Komiyama; Seth G N Grant; Christel Poujol; Daniel Choquet; Tilmann Achsel; Danielle Posthuma; August B Smit; Claudia Bagni
Journal:  Neuron       Date:  2013-09-18       Impact factor: 17.173

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10.  RNA-Binding Protein FXR1 Regulates p21 and TERC RNA to Bypass p53-Mediated Cellular Senescence in OSCC.

Authors:  Mrinmoyee Majumder; Reniqua House; Nallasivam Palanisamy; Shuo Qie; Terrence A Day; David Neskey; J Alan Diehl; Viswanathan Palanisamy
Journal:  PLoS Genet       Date:  2016-09-08       Impact factor: 5.917

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  6 in total

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Review 2.  Hypoxia and Extracellular Acidification as Drivers of Melanoma Progression and Drug Resistance.

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Review 5.  Interplay of RNA-Binding Proteins and microRNAs in Neurodegenerative Diseases.

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6.  NAPRT Expression Regulation Mechanisms: Novel Functions Predicted by a Bioinformatics Approach.

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  6 in total

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