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. 2011 Jan 18;108(5):1949–1954. doi: 10.1073/pnas.1008403108

Table 1.

Validated transcriptional targets activated by CUX1

mRNA expression (fold)
Hs578t shCUX1tetON
Gene ChIP IgG vs. input (fold) NmuMG (CUX1 vs. vector) + Dox − Dox
SAC
 AURKB +3.8 +2.6 −1.3 +7.0
 BUB1* +3.8 +3.6 −2.5 +5.6
 BUB3 +3.5 +2.4 −2.4 +7.5
 BUBR1 +1.7 +3.6 −2.2 +10.8
 CENPE* +10.8 +2.6 −1.6 +6.7
 MAD1L1 +4.7 +1.8 −1.5 +3.9
 MAD2L1* +2.7 +2.0 −2.6 +5.7
 TTK (MPS1) +2.0 +3.2 −1.2 +5.6
 NEK2 +2.5 +3.8 −1.4 +6.5
 ROD +3.6 +3.9 −1.5 +5.9
 ZW10 +3.1 +2.0 −1.8 +6.3
 ZWILCH +2.9 +5.0 −2.5 +4.3
Centromeric histone
 CENPA* +3.1 +1.9 −1.5 +5.8
Kinesin
 KIF2C* +2.3 +3.2 −1.4 +6.1
 KIFC1* +1.9 +2.3 −1.8 +9.4
Other functions
 CAMK2D* +2.9 +1.4 −1.9 +2.0
 COG7* +8.1 +1.6 −1.4 +1.3
 MFAP1* +4.3 +1.4 −1.7 +3.9
 NUDCD1* +3.7 +2.6 −1.2 +3.8
 RIN2* +4.2 +2.3 −1.6 +2.4
 SF3B3* +3.0 +2.0 −1.9 +4.6

Validation of p110 CUX1 transcriptional targets relevant to the establishment of bipolar mitoses. CUX1 transcriptional targets were identified by ChIP in Hs578T breast tumor cells. From left: column 1: asterisks (*) indicate genes previously identified in an siRNA screen for bipolar mitosis (18). Column 2: validation and measurement of promoter occupancy from independent ChIP assays using HeLa cells. Columns 3, 4, and 5: fold difference in mRNA expression measured by real-time PCR between NMuMG/CUX1 and control cells (column 3), Hs578t cells bearing a doxycyclin-inducible CUX1-specific shRNA, treated or not for 5 d with doxycycline (column 4), or after endogenous CUX1 expression was permitted after removal of doxycyclin for 3 d (column 5).