Masakazu Yoshida, Akihiko Ishimura, Minoru Terashima, Zanabazar Enkhbaatar, Naohito Nozaki, Kenji Satou, Takeshi Suzuki
Division of Functional Genomics, Cancer Research Institute, Kanazawa University, Kanazawa 920-1192, Ishikawa, Japan.
The Biochemical journal 2011 Aug 1PLU1 is a candidate oncogene that encodes H3K4 (Lys(4) of histone H3) demethylase. In the present study, we found that ectopic expression of PLU1 enhanced the invasive potential of the weakly invasive cells dependent on its demethylase activity. PLU1 was shown to repress the expression of the KAT5 gene through its H3K4 demethylation on the promoter. The regulation of KAT5 by PLU1 was suggested to be responsible for PLU1-induced cell invasion. First, knockdown of KAT5 similarly increased the invasive potential of the cells. Secondly, knockdown of PLU1 in the highly invasive cancer cells increased KAT5 expression and reduced the invasive activity. Thirdly, simultaneous knockdown of KAT5 partially relieved the suppression of cell invasion imposed by PLU1 knockdown. Finally, we found that CD82, which was transcriptionally regulated by KAT5, might be a candidate effector of cell invasion promoted by PLU1. The present study demonstrated a functional contribution of PLU1 overexpression with concomitant epigenetic dysregulation in cancer progression. © The Authors Journal compilation © 2011 Biochemical Society
Masakazu Yoshida, Akihiko Ishimura, Minoru Terashima, Zanabazar Enkhbaatar, Naohito Nozaki, Kenji Satou, Takeshi Suzuki. PLU1 histone demethylase decreases the expression of KAT5 and enhances the invasive activity of the cells. The Biochemical journal. 2011 Aug 1;437(3):555-64
PMID: 21574959
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