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. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: Nat Genet. 2013 Jan 27;45(3):253–261. doi: 10.1038/ng.2538

Figure 5. Functional relationship between β-catenin and FAT1 in the regulation of proliferation.

Figure 5

(a) Western blot showing co-transfection of β-catenin and FAT1 in chinese hamster ovary (CHO) cells.

(b) Growth curve demonstrating accelerated cell growth with over-expression of β-catenin, repressed with co-transfection with FAT1. Error bars represent 1 standard deviation. Experiments performed in CHO cells, in quadruplicate.

(c) BrdU (left) and cell cycle (right) assays demonstrate enhancement in DNA synthesis and cells entering S phase, after β-catenin over-expression, repressed with FAT1 co-transfection. Experiments performed in CHO cells, in triplicate.

(d) Western blot showing co-transfection of siRNAs targeting FAT1 and β-catenin, in U251 glioma cells.

(e) Growth curve demonstrating accelerated growth after FAT1 knockdown, reversed by concurrent knockdown of β-catenin. Error bars represent 1 standard deviation. Experiments performed in quadruplicate, in U251 glioma cells.

(f) BrdU (left) and cell cycle (right) assays demonstrate enhancement in DNA synthesis and cells entering S phase, after FAT1 knockdown, repressed with concurrent β-catenin knockdown, in U251 glioma cells. Experiments performed in triplicate. These data are shown with a 2nd set of siRNAs in Supplementary Fig. 3.

*p<.05, **p<.01, ***p<.001 ANOVA.