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. 2020 Nov 13;23(12):101795. doi: 10.1016/j.isci.2020.101795

Figure 2.

Figure 2

CBA-1 Regulates Histone Methylation

(A) CBA-1 did not inhibit the binding between β-catenin and TCF4. FLAG-tagged β-catenin and HA-tagged TCF4 were transfected separately into HEK293T cells. Equal amounts of β-catenin and TCF4 were mixed and immunoprecipitated by an anti-FLAG antibody. TCF4 was analyzed by an anti-HA antibody.

(B and C) CBA-1 significantly increased H3K9Me2 and H3K27Me3 in HEK293T and LS174T cells. Densitometry was analyzed using three western blot images (∗p < 0.05; n = 3).to new sentences: (B) CBA-1 significantly increased H3K9Me2 and H3K27Me3 in HEK293T cells. Densitometry was analyzed using three western blot images (∗p < 0.05; n = 3). (C) CBA-1 significantly increased H3K9Me2 and H3K27Me3 in LS174T cells. Densitometry was analyzed using three western blot images (∗p < 0.05; n = 3).

(D) CBA-1 increased H3K9Me2 on the promoters of Wnt target genes. The promoter sequences were analyzed by both standard PCR (left) and qPCR (right) (∗p < 0.01; n = 3).

(E) KDM3A, a potential target of CBA-1, overexpressed in CRC. Tumor: red. Normal tissue: gray.

(F) High levels of KDM3A correlated with poor CRC patient survival.