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Transcriptome analysis reveals altered cholesterol metabolism during the neurodegeneration in mouse scrapie model
Author(s) -
Xiang Wei,
Hummel Manuela,
Mitteregger Gerda,
Pace Claudia,
Windl Otto,
Mansmann Ulrich,
Kretzschmar Hans A.
Publication year - 2007
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2007.04566.x
Subject(s) - scrapie , biology , neurodegeneration , gene , transcriptome , microarray , gene expression , microarray analysis techniques , messenger rna , gene cluster , gene expression profiling , microbiology and biotechnology , genetics , medicine , disease , prion protein
To identify the dynamic transcriptional alterations in CNS during the development of prion disease, brains of scrapie‐infected mice and age‐matched, mock‐inoculated controls were analyzed immediately before inoculation and at different time points post‐inoculation using Affymetrix microarray technique. A total of 449 probe sets, representing 430 genes, showed differential expression between scrapie‐ and mock‐inoculated mice over the time course. These genes could be separated into two clusters according to expression patterns: the genes in cluster 1 demonstrated lower mRNA levels in scrapie‐infected brains when compared with mock‐inoculated brains, whereas genes in cluster 2 showed higher mRNA levels in scrapie‐infected brains. Functional analysis of differentially expressed genes revealed the most severely affected biological process: cholesterol metabolism. The expression patterns of the cholesterol‐related genes indicated an inhibited cholesterol synthesis in the diseased brains. Conspicuously, a number of cluster 1 genes, including some of cholesterol‐related genes, showed not only decreasing mRNA levels in scrapie‐infected brains but also increasing mRNA levels in mock‐inoculated brains with increasing age. Quantitative RT‐PCR analysis of some cholesterol‐related genes in untreated mice suggested that changes of the examined genes observed in mock‐inoculated brains are mainly age related. This finding indicated a link between age‐related genes and scrapie‐associated neurodegeneration.