Literature DB >> 12460546

Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein.

Annette Schenck1, Veronique Van de Bor, Barbara Bardoni, Angela Giangrande.   

Abstract

FMRP belongs to a family of widely expressed proteins that contain RNA-binding domains. Although lack of human FMRP results in mental retardation, correlated with subtle synaptic changes, the precise role of FMRP remains elusive. The Drosophila genome contains a single gene homologous to the FXR family. We show that dFMR1 is subjected to transcriptional and posttranscriptional regulation during development and that it homomerizes, like its human counterpart. dFMR1 profile of expression recapitulates that of the human FXR protein family: it is highly enriched in muscles, in central nervous system and in gonads. In the larval brain, anti-dFMR1 also recognizes mushroom bodies, a centre that mediates learning and memory. These features make the fly an ideal system to analyse the role of the FXR family and to identify genes in the FMRP pathway.

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Year:  2002        PMID: 12460546     DOI: 10.1006/nbdi.2002.0510

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  13 in total

1.  Genealogical correspondence of a forebrain centre implies an executive brain in the protostome-deuterostome bilaterian ancestor.

Authors:  Gabriella H Wolff; Nicholas J Strausfeld
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-01-05       Impact factor: 6.237

2.  Molecular and genetic analysis of the Drosophila model of fragile X syndrome.

Authors:  Charles R Tessier; Kendal Broadie
Journal:  Results Probl Cell Differ       Date:  2012

3.  Disruption of the MAP1B-related protein FUTSCH leads to changes in the neuronal cytoskeleton, axonal transport defects, and progressive neurodegeneration in Drosophila.

Authors:  Alexandre Bettencourt da Cruz; Martin Schwärzel; Sabine Schulze; Mahtab Niyyati; Martin Heisenberg; Doris Kretzschmar
Journal:  Mol Biol Cell       Date:  2005-03-16       Impact factor: 4.138

Review 4.  From genetics to structure to function: exploring sleep in Drosophila.

Authors:  Daniel Bushey; Chiara Cirelli
Journal:  Int Rev Neurobiol       Date:  2011       Impact factor: 3.230

5.  A non-canonical start codon in the Drosophila fragile X gene yields two functional isoforms.

Authors:  R W Beerman; T A Jongens
Journal:  Neuroscience       Date:  2011-02-17       Impact factor: 3.590

6.  Argonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects.

Authors:  Anita S-R Pepper; Rebecca W Beerman; Balpreet Bhogal; Thomas A Jongens
Journal:  PLoS One       Date:  2009-10-27       Impact factor: 3.240

Review 7.  The fragile-X premutation: a maturing perspective.

Authors:  Paul J Hagerman; Randi J Hagerman
Journal:  Am J Hum Genet       Date:  2004-03-29       Impact factor: 11.025

8.  Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships.

Authors:  Ben Tucker; Robert Richards; Michael Lardelli
Journal:  Dev Genes Evol       Date:  2004-09-17       Impact factor: 0.900

Review 9.  The cyclic AMP phenotype of fragile X and autism.

Authors:  Daniel J Kelley; Anita Bhattacharyya; Garet P Lahvis; Jerry C P Yin; Jim Malter; Richard J Davidson
Journal:  Neurosci Biobehav Rev       Date:  2008-06-17       Impact factor: 8.989

Review 10.  Modeling Fragile X Syndrome in Drosophila.

Authors:  Małgorzata Drozd; Barbara Bardoni; Maria Capovilla
Journal:  Front Mol Neurosci       Date:  2018-04-16       Impact factor: 5.639

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