Yao Ya-Li, Yang Wen-Ming
Institute of Zoology, Academia Sinica, Taipei 115, Taiwan, Republic of China.
J Biol Chem. 2003 Oct 24;278(43):42560-8. doi: 10.1074/jbc.M302955200. Epub 2003 Aug 13.
The metastasis-associated protein MTA1 has been shown to express differentially to high levels in metastatic cells. MTA2, which is homologous to MTA1, is a component of the NuRD ATP-dependent chromatin remodeling and histone deacetylase complex. Here we report evidence that although both human MTA1 and MTA2 repress transcription specifically, are located in the nucleus, and contain associated histone deacetylase activity, they exist in two biochemically distinct protein complexes and may perform different functions pertaining to tumor metastasis. Specifically, both MTA1 and MTA2 complexes exert histone deacetylase activity. However, the MTA1 complex contained HDAC1/2, RbAp46/48, and MBD3, but not Sin3 or Mi2, two important components of the MTA2 complex. Moreover, the MTA2 complex is similar to the HDAC1 complex, suggesting a housekeeping role of the MTA2 complex. The MTA1 complex could be further separated, resulting in a core MTA1-HDAC complex, showing that the histone deacetylase activity and transcriptional repression activity were integral properties of the MTA1 complex. Finally, MTA1, unlike MTA2, did not interact with the pleotropic transcription factor YY1 or the immunophilin FKBP25. We suggest that MTA1 associates with a different set of transcription factors from MTA2 and that this property may contribute to the metastatic potential of cells overexpressing MTA1. We also report the finding of human MTA3, which is highly homologous to both MTA1 and MTA2. However, MTA3 does not repress transcription to a significant level and appears to have a diffused pattern of subcellular localization, suggesting a biological role distinct from that of the other two MTA proteins.
转移相关蛋白MTA1在转移细胞中已被证明有高水平的差异表达。与MTA1同源的MTA2是NuRD ATP依赖的染色质重塑和组蛋白去乙酰化酶复合物的一个组成部分。在此我们报告如下证据:尽管人类MTA1和MTA2均特异性抑制转录、定位于细胞核并具有相关的组蛋白去乙酰化酶活性,但它们存在于两种生化性质不同的蛋白质复合物中,并且可能在肿瘤转移方面发挥不同功能。具体而言,MTA1和MTA2复合物均具有组蛋白去乙酰化酶活性。然而,MTA1复合物包含HDAC1/2、RbAp46/48和MBD3,但不包含MTA2复合物的两个重要组分Sin3或Mi2。此外,MTA2复合物与HDAC1复合物相似,提示MTA2复合物具有管家功能。MTA1复合物能够进一步分离,产生一个核心MTA1-HDAC复合物,表明组蛋白去乙酰化酶活性和转录抑制活性是MTA1复合物的固有特性。最后,与MTA2不同,MTA1不与多效转录因子YY1或亲免蛋白FKBP25相互作用。我们认为,MTA1与一组不同于MTA2的转录因子相关联,并且这一特性可能有助于过表达MTA1的细胞的转移潜能。我们还报告了人类MTA3的发现,它与MTA1和MTA2均高度同源。然而,MTA3不会显著抑制转录,并且似乎具有弥散的亚细胞定位模式,提示其生物学作用不同于其他两种MTA蛋白。