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. 2021 Jan 13;95(3):e01970-20. doi: 10.1128/JVI.01970-20

TABLE 1.

Differential gene expression in SAMHD1 KO THP-1 cells compared to control cells

Gene symbol Entrez gene name mRNA fold change Expected activationa
KRAS KRAS proto-oncogene, GTPase −5.42 Up
HDAC2 Histone deacetylase 2 −3.90 Down
TAB2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 −3.37 Up
MAP3K7b Mitogen-activated protein kinase kinase kinase 7 −3.25 Up
IGF2R Insulin-like growth factor 2 receptor −2.95 Up
PIK3R1 Phosphoinositide-3-kinase regulatory subunit 1 2.23 Up
PRKACB Protein kinase cAMP-activated catalytic subunit beta 2.12 Up
PIK3C3 Phosphatidylinositol 3-kinase catalytic subunit type 3 2.23 Up
FCER1G Fc fragment of IgE receptor Ig 2.51 Up
IL18 Interleukin 18 3.49 Up
CD40 CD40 molecule 3.63 Up
TLR6 Toll-like receptor 6 3.68 Up
AKT3 AKT serine/threonine kinase 3 10.71 Up
a

The expected activation of genes whose mRNA expression levels were significantly altered in THP-1 SAMHD1 KO cells relative to control cells (fold change > 2; P ≤ 1 × 10−4) was predicted through ingenuity pathway analysis (IPA) of the microarray data. RNA extracted from triplicate THP-1 control and SAMHD1 KO cells was analyzed by Affymetrix Clariom D microarray (29).

b

MAP3K7 is also known as transforming growth factor β-activated kinase 1 (TAK1).