Abstract
Histone deacetylase (HDAC) plays a key role in gene expression, by suppressing the transcription of a number of target genes. Identification of such genes is important for deciphering the functional role of HDAC. Here, using cancer gene-focused DNA microarray analysis, we identified plakoglobin as a new target gene of HDAC. Functional inhibition of HDAC by its specific inhibitors induced the expression of plakoglobin by eight-fold in human fibrosarcoma HT1080 cells. However, the expression of β-catenin, which is closely related to plakoglobin, was not altered, implying the specific function of HDAC in plakoglobin expression. Using antiacetyl-H4 antibody, chromatin immunoprecipitation analysis revealed that the distal region (-945 ∼ -646) of the promoter of plakoglobin is responsible for the HDAC-mediated repression of the gene. Moreover, the induced expression of plakoglobin by the inhibition of HDAC activated the Tcf/ Lef-dependent luciferase reporter gene, a well-known downstream effector of the Wnt signaling pathway. Furthermore, transient transfection of plakoglobin also activated Tcf/Lef reporter gene expression. Taken together, our results demonstrate that plakoglobin is a new target gene governed by HDAC, and that it acts as an oncogene in HT1080 cells.
Original language | English |
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Pages (from-to) | 1704-1711 |
Number of pages | 8 |
Journal | Oncogene |
Volume | 23 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2004 Mar 4 |
Bibliographical note
Funding Information:We are grateful to Drs ER Fearon for plasmid constructs, and to SY Rha and HC Chung for their help of cDNA microarray analysis. We also thank Dr H Kleinman for critical reading and comments of the manuscript. This study was supported by a grant from the Korea Science & Engineering Foundation (R01-1999-00121-0) and the Brain Korea 21 Project.
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Genetics
- Cancer Research