Yamamoto T, Horikoshi M
Laboratory of Developmental Biology, Department of Cellular Biology, Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113, Japan.
J Biol Chem. 1997 Dec 5;272(49):30595-8. doi: 10.1074/jbc.272.49.30595.
Tip60, originally isolated as an HIV-1-Tat interactive protein, contains an evolutionarily conserved domain with yeast silencing factors. We demonstrate here direct biochemical evidence that this domain of Tip60 has histone acetyltransferase activity. The purified recombinant effectively acetylates H2A, H3, and H4 but not H2B of core histone mixtures. This substrate specificity has not been observed among histone acetyltransferases analyzed to date. These results indicate that Tip60 is a histone acetyltransferase with a novel property, suggesting that Tip60 and its related factors may introduce a distinct alteration on chromatin.
Tip60最初作为一种HIV-1-Tat相互作用蛋白被分离出来,它含有一个与酵母沉默因子在进化上保守的结构域。我们在此展示了直接的生化证据,表明Tip60的这一结构域具有组蛋白乙酰转移酶活性。纯化的重组体可有效地使核心组蛋白混合物中的H2A、H3和H4发生乙酰化,但不能使H2B乙酰化。这种底物特异性在迄今为止分析的组蛋白乙酰转移酶中尚未观察到。这些结果表明Tip60是一种具有新特性的组蛋白乙酰转移酶,这表明Tip60及其相关因子可能会在染色质上引入一种独特的改变。