转基因小鼠
转基因
生物
基因表达
基因
基因组
基因表达谱
遗传学
病理
计算生物学
细胞生物学
分子生物学
医学
作者
Mar Matarín,Derviş A. Salih,Marina V. Yasvoina,Damian M. Cummings,Sebastian Guelfi,Wenfei Liu,Muzammil A. Nahaboo Solim,Thomas G. Moens,Rocio Moreno Paublete,Shabinah S. Ali,Marina Perona,Roshni Desai,Kenneth J. Smith,Judy Latcham,Michael Fulleylove,Jill Richardson,John Hardy,Frances A. Edwards
出处
期刊:Cell Reports
[Cell Press]
日期:2015-01-22
卷期号:10 (4): 633-644
被引量:273
标识
DOI:10.1016/j.celrep.2014.12.041
摘要
We provide microarray data comparing genome-wide differential expression and pathology throughout life in four lines of "amyloid" transgenic mice (mutant human APP, PSEN1, or APP/PSEN1) and "TAU" transgenic mice (mutant human MAPT gene). Microarray data were validated by qPCR and by comparison to human studies, including genome-wide association study (GWAS) hits. Immune gene expression correlated tightly with plaques whereas synaptic genes correlated negatively with neurofibrillary tangles. Network analysis of immune gene modules revealed six hub genes in hippocampus of amyloid mice, four in common with cortex. The hippocampal network in TAU mice was similar except that Trem2 had hub status only in amyloid mice. The cortical network of TAU mice was entirely different with more hub genes and few in common with the other networks, suggesting reasons for specificity of cortical dysfunction in FTDP17. This Resource opens up many areas for investigation. All data are available and searchable at http://www.mouseac.org.
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