Takahashi Y, Kahyo T, Toh-E A, Yasuda H, Kikuchi Y
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
J Biol Chem. 2001 Dec 28;276(52):48973-7. doi: 10.1074/jbc.M109295200. Epub 2001 Sep 27.
SUMO1/Smt3, a ubiquitin-like protein modifier, is known to conjugate to other proteins and modulate their functions in various important processes. Similar to the ubiquitin conjugation system, SUMO/Smt3 is transferred to substrate lysine residues through the thioester cascade of E1 (activating enzyme) and E2 (conjugating enzyme). In our previous report (Takahashi, Y., Toh-e, A., and Kikuchi, Y. (2001) Gene 275, 223-231), we showed that Siz1/Ull1 (YDR409w) of budding yeast, a member of the human PIAS family containing a RING-like domain, is a strong candidate for SUMO1/Smt3 ligase because the SUMO1/Smt3 modification of septin components was abolished in the ull1 mutant and Ull1 associated with E2 (Ubc9) and the substrates (septin components) in immunoprecipitation experiments. Here we have developed an in vitro Smt3 conjugation system for a septin component (Cdc3) using purified recombinant proteins. In this system, Ull1 is additionally required as well as E1 (Sua1.Uba2 complex), E2 (Ubc9), and ATP. A cysteine residue of the RING-like domain was essential for the conjugation both in vivo and in vitro. Furthermore, a region containing the RING-like domain directly interacted with Ubc9 and Cdc3. Thus, this SUMO/Smt3 ligase functions as an adaptor between E2 and the target proteins.
SUMO1/Smt3是一种类泛素蛋白修饰因子,已知它能与其他蛋白质结合并在各种重要过程中调节其功能。与泛素结合系统类似,SUMO/Smt3通过E1(激活酶)和E2(结合酶)的硫酯级联反应转移到底物赖氨酸残基上。在我们之前的报告中(高桥洋、东枝昭、菊池洋(2001年),《基因》275卷,第223 - 231页),我们表明,出芽酵母的Siz1/Ull1(YDR409w),一种含有类RING结构域的人类PIAS家族成员,是SUMO1/Smt3连接酶的有力候选者,因为在ull1突变体中,septin成分的SUMO1/Smt3修饰被消除,并且在免疫沉淀实验中,Ull1与E2(Ubc9)和底物(septin成分)相关联。在这里,我们使用纯化的重组蛋白开发了一种用于septin成分(Cdc3)的体外Smt3结合系统。在这个系统中,除了E1(Sua1.Uba2复合物)、E2(Ubc9)和ATP外,还需要Ull1。类RING结构域的一个半胱氨酸残基对于体内和体外的结合都是必不可少的。此外,包含类RING结构域的区域直接与Ubc9和Cdc3相互作用。因此,这种SUMO/Smt3连接酶作为E2和靶蛋白之间的衔接子发挥作用。