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. Author manuscript; available in PMC: 2012 Feb 29.
Published in final edited form as: J Biol Chem. 2007 Jul 1;282(34):24866–24872. doi: 10.1074/jbc.M703902200

Table 1.

Effects of Shield-1 on Gene Expression in NIH3T3 Cells

Upregulated Genes
Clone ID Gene Symbol Gene description Fold Change (FDR*)
10 nM 100 nM 1 μM
mSQ030922 Epb4.1l2 Erythrocyte protein band 4.1-like 2 2.2 (<0.1%)
mSQ001430 Csnk1e Casein kinase 1, epsilon 2.7 (<0.1%)
mSQ002857 Tcfe3 Transcription factor E3 1.9 (27.5%)
Downregulated Genes
Clone ID Gene Symbol Gene description Fold Change (FDR*)
10 nM 100 nM 1 μM
mSQ036549 MtCrVgp3 Murine type C retrovirus −11.3 (<0.1%)
mSQ009285 4930422M22Rik RIKEN cDNA 4930422M22 gene −2.2 (<0.1%)
mSQ007437 A430110N23 hypothetical protein A430110N23 −2.1 (<0.1%)
mSQ014243 Ptpn1 Protein tyrosine phosphatase, non- receptor type 1 −1.7 (<0.1%)
mSQ001772 Npas4 Neuronal PAS domain protein 4 −1.7 (22.7%)
mSQ028092 Shkbp1 Sh3kbp1 binding protein 1 −2.3 (22.7%)
*

NIH3T3 cells in triplicate were cultured in media and mock-treated or treated with 10 nM, 100 nM or 1 μM Shield-1 for 24 hours. Total RNA from each of the twelve samples was extracted and hybridized to the MEEBO oligonucleotide array. The false discovery rate (FDR) was obtained using unpaired two-class Significance Analysis of Microarrays (SAM), and genes whose mRNA levels changed significantly upon Shield-1 treatment were identified.