Stowers Institute for Medical Research, Kansas City, Missouri 64110, USA.
Mol Cell Proteomics. 2012 Dec;11(12):1815-28. doi: 10.1074/mcp.M112.020255. Epub 2012 Sep 14.
Here we describe the function of a previously uncharacterized protein, named family with sequence similarity 60 member A (FAM60A) that maps to chromosome 12p11 in humans. We use quantitative proteomics to determine that the main biochemical partners of FAM60A are subunits of the Sin3 deacetylase complex and show that FAM60A resides in active HDAC complexes. In addition, we conduct gene expression pathway analysis and find that FAM60A regulates expression of genes that encode components of the TGF-beta signaling pathway. Moreover, our studies reveal that loss of FAM60A or another component of the Sin3 complex, SDS3, leads to a change in cell morphology and an increase in cell migration. These studies reveal the function of a previously uncharacterized protein and implicate the Sin3 complex in suppressing cell migration.
在这里,我们描述了一个以前未被描述的蛋白质的功能,该蛋白质名为家族与序列相似性 60 成员 A(FAM60A),它位于人类染色体 12p11 上。我们使用定量蛋白质组学来确定 FAM60A 的主要生化伙伴是 Sin3 去乙酰化酶复合物的亚基,并表明 FAM60A 存在于活性 HDAC 复合物中。此外,我们进行了基因表达途径分析,发现 FAM60A 调节编码 TGF-β信号通路组成部分的基因的表达。此外,我们的研究表明,FAM60A 或 Sin3 复合物的另一个成分 SDS3 的缺失会导致细胞形态的改变和细胞迁移的增加。这些研究揭示了一个以前未被描述的蛋白质的功能,并暗示 Sin3 复合物在抑制细胞迁移方面的作用。