Metastasis-associated protein 1 (MTA1) is an essential downstream effector of the c-MYC oncoprotein

Xiao-yong Zhang(The Wistar Institute), Lauren M. DeSalle(The Wistar Institute), Jagruti Patel(The Wistar Institute), Anthony J. Capobianco(The Wistar Institute), Duonan Yu(The Wistar Institute), Andrei Thomas‐Tikhonenko(The Wistar Institute), Steven B. McMahon(The Wistar Institute)
Proceedings of the National Academy of Sciences
September 19, 2005
Cited by 118Open Access
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Abstract

The c-myc oncogene is among the most commonly overexpressed genes in human cancer. c-myc encodes a basic helix-loop-helix/leucine zipper (bHLH/LZ) transcription factor (c-MYC) that activates a cascade of downstream targets that ultimately mediate cellular transformation. Although a large number of genes are regulated by c-MYC, only a few have been functionally linked to c-MYC-mediated transformation. By expression profiling, the metastasis-associated protein 1 (MTA1) gene was identified here as a target of the c-MYC oncoprotein in primary human cells, a result confirmed in human cancer cells. MTA1 itself has been previously implicated in cellular transformation, in part through its ability to regulate the epithelial-to-mesenchymal transition and metastasis. MTA1 is a component of the Mi-2/nucleosome remodeling and deacetylating (NURD) complex that contains both histone deacetylase and nucleosome remodeling activity. The data reported here demonstrate that endogenous c-MYC binds to the genomic MTA1 locus and recruits transcriptional coactivators. Most importantly, short hairpin RNA (shRNA)-mediated knockdown of MTA1 blocks the ability of c-MYC to transform mammalian cells. These data implicate MTA1 and the Mi-2/NURD complex as one of the first downstream targets of c-MYC function that are essential for the transformation potential of c-MYC.


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