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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2010-10-15
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pubmed:abstractText |
The endoplasmic reticulum (ER) stress-mediated pathway is involved in a wide range of human neurodegenerative disorders. Hence, molecules that regulate the ER stress response represent potential candidates as drug targets to tackle these diseases. In previous studies we demonstrated that upon acetylation the reticulon-1C (RTN-1C) variant of the reticulon family leads to inhibition of histone deacetylase (HDAC) enzymatic activity and endoplasmic reticulum stress-dependent apoptosis. Here, by microarray analysis of the whole human genome we found that RTN-1C is able to specifically regulate gene expression, modulating transcript clusters which have been implicated in the onset of neurodegenerative disorders. Interestingly, we show that some of the identified genes were also modulated in vivo in a brain-specific mouse model overexpressing RTN-1C. These data provide a basis for further investigation of RTN-1C as a potential molecular target for use in therapy and as a specific marker for neurological diseases.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1095-953X
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pubmed:author |
pubmed-author:BiancolellaMichelaM,
pubmed-author:BlandiniFabioF,
pubmed-author:CorazzariMarcoM,
pubmed-author:Di SanoFedericaF,
pubmed-author:FaziBarbaraB,
pubmed-author:MehdawyBisanB,
pubmed-author:MinellaDanielaD,
pubmed-author:MorenoSandraS,
pubmed-author:NardacciRobertaR,
pubmed-author:NisticòRobertR,
pubmed-author:NovelliGiuseppeG,
pubmed-author:PiacentiniMauroM,
pubmed-author:SepeSaraS
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pubmed:copyrightInfo |
Copyright © 2010 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
634-44
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pubmed:meshHeading |
pubmed-meshheading:20708685-Animals,
pubmed-meshheading:20708685-Apoptosis,
pubmed-meshheading:20708685-Blotting, Western,
pubmed-meshheading:20708685-Brain,
pubmed-meshheading:20708685-Cell Line, Tumor,
pubmed-meshheading:20708685-Endoplasmic Reticulum,
pubmed-meshheading:20708685-Fluorescent Antibody Technique,
pubmed-meshheading:20708685-Gene Expression Regulation,
pubmed-meshheading:20708685-Humans,
pubmed-meshheading:20708685-Immunohistochemistry,
pubmed-meshheading:20708685-In Situ Hybridization,
pubmed-meshheading:20708685-Mice,
pubmed-meshheading:20708685-Mice, Transgenic,
pubmed-meshheading:20708685-Microscopy, Electron, Transmission,
pubmed-meshheading:20708685-Nerve Tissue Proteins,
pubmed-meshheading:20708685-Neuroblastoma,
pubmed-meshheading:20708685-Neurodegenerative Diseases,
pubmed-meshheading:20708685-Neurons,
pubmed-meshheading:20708685-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:20708685-Patch-Clamp Techniques,
pubmed-meshheading:20708685-Reverse Transcriptase Polymerase Chain Reaction
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pubmed:year |
2010
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pubmed:articleTitle |
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain.
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pubmed:affiliation |
Department of Biology, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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