Desterro J M, Rodriguez M S, Kemp G D, Hay R T
School of Biomedical Science, University of St. Andrews, St. Andrews, Fife KY169ST Scotland.
J Biol Chem. 1999 Apr 9;274(15):10618-24. doi: 10.1074/jbc.274.15.10618.
The ubiquitin-like protein SUMO-1 is conjugated to a variety of proteins including Ran GTPase-activating protein 1 (RanGAP1), IkappaBalpha, and PML. SUMO-1-modified proteins display altered subcellular targeting and/or stability. We have purified the SUMO-1-activating enzyme from human cells and shown that it contains two subunits of 38 and 72 kDa. Isolation of cDNAs for each subunit indicates that they are homologous to ubiquitin-activating enzymes and to the Saccharomyces cerevisiae enzymes responsible for conjugation of Smt3p and Rub-1p. In vitro, recombinant SAE1/SAE2 (SUMO-1-activating enzyme) was capable of catalyzing the ATP-dependent formation of a thioester linkage between SUMO-1 and SAE2. The addition of the SUMO-1-conjugating enzyme Ubch9 resulted in efficient transfer of the thioester-linked SUMO-1 from SAE2 to Ubch9. In the presence of SAE1/SAE2, Ubch9, and ATP, SUMO-1 was efficiently conjugated to the protein substrate IkappaBalpha. As SAE1/SAE2, Ubch9, SUMO-1, and IkappaBalpha are all homogeneous, recombinant proteins, it appears that SUMO-1 conjugation of IkappaBalpha in vitro does not require the equivalent of an E3 ubiquitin protein ligase activity.
类泛素蛋白SUMO-1可与多种蛋白质共价结合,包括Ran GTP酶激活蛋白1(RanGAP1)、IκBα和早幼粒细胞白血病蛋白(PML)。SUMO-1修饰的蛋白质表现出亚细胞定位和/或稳定性的改变。我们已经从人细胞中纯化了SUMO-1激活酶,并表明它包含两个分别为38 kDa和72 kDa的亚基。每个亚基的cDNA分离表明,它们与泛素激活酶以及酿酒酵母中负责Smt3p和Rub-1p共价结合的酶同源。在体外,重组SAE1/SAE2(SUMO-1激活酶)能够催化SUMO-1与SAE2之间形成依赖ATP的硫酯键。添加SUMO-1结合酶Ubch9可使硫酯连接的SUMO-1从SAE2高效转移至Ubch9。在SAE1/SAE2、Ubch9和ATP存在的情况下,SUMO-1可高效地与蛋白底物IκBα共价结合。由于SAE1/SAE2、Ubch9、SUMO-1和IκBα均为均一的重组蛋白,因此体外IκBα的SUMO-1共价结合似乎不需要相当于E3泛素蛋白连接酶的活性。