Skip to main content
. 2010 Sep 1;9(17):3552–3564. doi: 10.4161/cc.9.17.12792

Table 1.

Relative mRNA quantitations

Gene RPKM HeLa RPKM H9 Function
Gapdh 1230 1727 Internal control
Nanog 0.05 21.8 Stem cell marker
Sox2 0.00 70.6 Stem cell marker
Lin28 0.03 285.0 Stem cell marker
Oct3/4 0.2 560 Stem cell marker
TLR3 1.3 0.1 IFNβ induction
TICAM-1/TRIF 11.8 0.4 IFNβ induction
RIG-I 0.8 1.0 IFNβ induction
STING/MITA 18.1 0.1 IFNβ induction
TBK1 6.0 2.0 IFNβ induction
IKBKE 2.0 3.3 IFNβ induction
MDA5 1.9 0.2 IFNβ induction
VISA/IPS-1/MAVS 6.9 6.8 IFNβ induction
EYA4 48.6 0.0 IFNβ induction
PKR 14.1 4.1 IFNβ induction
NFκB1 8.3 1.8 IFNβ induction
NFκB2 16.2 6.3 IFNβ induction
IκB 6.3 4.6 IFNβ induction
IRF3 10.9 19.3 IFNβ induction
IRF7 0.4 2.6 IFNβ induction
OAS1 8.7 0.05 OAS, RNAseL pathway
OAS3 12.7 0.4 OAS, RNAseL pathway
RNAse L 0.68 0.1 OAS, RNAseL pathway
ADAR1 58.3 53.5 Editing (nuclear)

Relative expression of genes involved in the cytoplasmic pathways to dsRNA between HeLa and H9 cells. Equal amounts of poly(A)+ RNAs were analyzed using the Illumina Genome Analyzer. The relative levels of mRNA expression are reported as the normalized number of reads that mapped to the annotated exons of each gene (# of reads per thousand nucleotides of exons, per million total reads [RPKM]). Higher numbers are positively correlated to higher levels of gene expression. Reads from one experiment are reported, but similar relative levels of mRNA expression were seen in two other independent sequencing experiments.