کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4324972 1613958 2012 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparative analyses of Purkinje cell gene expression profiles reveal shared molecular abnormalities in models of different polyglutamine diseases
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Comparative analyses of Purkinje cell gene expression profiles reveal shared molecular abnormalities in models of different polyglutamine diseases
چکیده انگلیسی

Polyglutamine (PolyQ) diseases have common features that include progressive selective neurodegeneration and the formation of protein aggregates. There is growing evidence to suggest that critical nuclear events lead to transcriptional alterations in PolyQ diseases such as spinocerebellar ataxia type 7 (SCA7) and Huntington's disease (HD), conditions which share a cerebellar degenerative phenotype. Taking advantage of laser capture microdissection technique, we compared the Purkinje cell (PC) gene expression profiles of two transgenic polyQ mouse models (HD: R6/2; SCA7: P7E) by microarray analysis that was validated by real time quantitative PCR. A large number of transcriptional alterations were detected in the R6/2 transgenic model of HD. Similar decreases in the same mRNAs, such as phospholipase C, β 3, purkinje cell protein 2 (Pcp2) and aldolase C, were found in both models. A decrease in aldolase C and phospholipase C, β 3, may lead to an increase in the vulnerability of PCs to excitotoxic events. Furthermore, downregulation of mRNAs mediated by the Pcp2-promoter is common in both models. Thus, our data reveal shared molecular abnormalities in different polyQ disorders.


► Huntington's disease and spinocerebellar ataxia type 7 are polyglutamine diseases.
► Common features include progressive selective neurodegeneration and cerebellar symptoms.
► Comparison of two models for these disorders revealed some of the same mRNA changes.
► Similar decreases in Purkinje cells were found for Plcb3, Pcp2 and Aldoc.
► Thus, our data point to shared molecular abnormalities in different polyglutamine disorders.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1481, 24 October 2012, Pages 37–48
نویسندگان
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