Frohloff Frank, Jablonowski Daniel, Fichtner Lars, Schaffrath Raffael
Institut für Genetik, Biologicum, Martin-Luther-Universität Halle-Wittenberg, Weinbergweg 10, Germany.
J Biol Chem. 2003 Jan 10;278(2):956-61. doi: 10.1074/jbc.M210060200. Epub 2002 Nov 6.
In response to the Kluyveromyces lactis zymocin, the gamma-toxin target (TOT) function of the Saccharomyces cerevisiae RNA polymerase II (pol II) Elongator complex prevents sensitive strains from cell cycle progression. Studying Elongator subunit communications, Tot1p (Elp1p), the yeast homologue of human IKK-associated protein, was found to be essentially involved in maintaining the structural integrity of Elongator. Thus, the ability of Tot2p (Elp2p) to interact with the HAT subunit Tot3p (Elp3p) of Elongator and with subunit Tot5p (Elp5p) is dependent on Tot1p (Elp1p). Also, the association of core-Elongator (Tot1-3p/Elp1-3p) with HAP (Elp4-6p/Tot5-7p), the second three-subunit subcomplex of Elongator, was found to be sensitive to loss of TOT1 (ELP1) gene function. Structural integrity of the HAP complex itself requires the ELP4/TOT7, ELP5/TOT5, and ELP6/TOT6 genes, and elp6Delta/tot6Delta as well as elp4Delta/tot7Delta cells can no longer promote interaction between Tot5p (Elp5p) and Tot2p (Elp2p). The association between Elongator and Tot4p (Kti12p), a factor that may modulate the TOT activity of Elongator, requires Tot1-3p (Elp1-3p) and Tot5p (Elp5p), indicating that this contact requires a preassembled holo-Elongator complex. Tot4p also binds pol II hyperphosphorylated at its C-terminal domain Ser(5) raising the possibility that Tot4p bridges the contact between Elongator and pol II.
针对乳酸克鲁维酵母酶菌素,酿酒酵母RNA聚合酶II(pol II)延伸因子复合物的γ-毒素靶点(TOT)功能可阻止敏感菌株的细胞周期进程。在研究延伸因子亚基间的相互作用时,发现人IKK相关蛋白的酵母同源物Tot1p(Elp1p)在维持延伸因子的结构完整性方面至关重要。因此,Tot2p(Elp2p)与延伸因子的HAT亚基Tot3p(Elp3p)以及亚基Tot5p(Elp5p)相互作用的能力取决于Tot1p(Elp1p)。此外,还发现核心延伸因子(Tot1 - 3p/Elp1 - 3p)与延伸因子的第二个三聚体亚复合物HAP(Elp4 - 6p/Tot5 - 7p)的结合对TOT1(ELP1)基因功能的丧失敏感。HAP复合物自身的结构完整性需要ELP4/TOT7、ELP5/TOT5和ELP6/TOT6基因,elp6Delta/tot6Delta以及elp4Delta/tot7Delta细胞不再能促进Tot5p(Elp5p)和Tot2p(Elp2p)之间的相互作用。延伸因子与Tot4p(Kti12p)之间的结合需要Tot1 - 3p(Elp1 - 3p)和Tot5p(Elp5p),Tot4p是一种可能调节延伸因子TOT活性的因子,这表明这种相互作用需要预先组装好的全延伸因子复合物。Tot4p还结合其C末端结构域Ser(5)处高度磷酸化的pol II,这增加了Tot4p在延伸因子和pol II之间建立联系的可能性。