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. Author manuscript; available in PMC: 2015 Jun 1.
Published in final edited form as: J Neurochem. 2014 Feb 9;129(6):932–939. doi: 10.1111/jnc.12660

Table 1.

Quantitative PCR Validates Gene Expression Changes Revealed by Microarray

Entrez Gene
ID
gene
Symbol
microarray assay quantitative PCR
folds changed in astrocytes folds changed in
astrocyte culture
folds changed in
rat spinal cord
3 days 4 days 6 days
114592 Aurkb 4.8 6.1 9.7 6 4
24825 Tf 3.6 2.5 2.0 4 3
312707 Lrrc23 3.1 3.0 2.4 3 2
266803 Sostdc1 2.2 2.0 1.2 4 3
24231 C2 2.1 2.3 2.5 3 8
25742 S100b 2.1 1.5 1.6 2 5
170496 Lcn2 2.1 3.0 2.1 5 12
245920 Cxcl10 1.8 2.3 1.9 2 6
89824 Chi3l1 1.8 1.5 1.2 2 9
282583 Fbln2 2.4 3.0 3.3 3 4
59107 Ltbp1 2.5 2.2 3.7 3 3
25118 Itga1 4.2 3.2 3.6 4 3
24484 Igfbp3 5.7 4.0 4.8 5 6

Notes: For quantitative PCR, mRNA was extracted from astrocyte culture or rat spinal cord and reverse-transcribed into cDNA pools. Genes except Chi3L1 were selected for PCR verification based on their fold change > 2 at any of the three induction times (3, 4, or 6 days after Dox withdrawal). Chi3L1 is reported to be upregulated in neurodegenerative diseases and thus its expression in rat tissue was further analyzed by PCR. Quantitative PCR amplified cDNA of interested genes and also amplified the cDNA of L17. The levels of each mRNA in TDP-43M337V expressing cells or tissues were normalized to those in GFAP-tTA single transgenic cells or tissues and were expressed as the folds changed. Numbers in red indicate the increase in the folds of gene expression and numbers in blue indicate the decrease in the folds of gene expression.