Urakov V N, Valouev I A, Lewitin E I, Paushkin S V, Kosorukov V S, Kushnirov V V, Smirnov V N, Ter-Avanesyan M D
Institute of Experimental Cardiology, Cardiology Research Center, Moscow, 121552, Russia.
BMC Mol Biol. 2001;2:9. doi: 10.1186/1471-2199-2-9. Epub 2001 Aug 24.
Termination of translation in eukaryotes is controlled by two interacting polypeptide chain release factors, eRFl and eRF3. eRFl recognizes nonsense codons UAA, UAG and UGA, while eRF3 stimulates polypeptide release from the ribosome in a GTP- and eRFl - dependent manner. Recent studies has shown that proteins interacting with these release factors can modulate the efficiency of nonsense codon readthrough.
We have isolated a nonessential yeast gene, which causes suppression of nonsense mutations, being in a multicopy state. This gene encodes a protein designated Itt1p, possessing a zinc finger domain characteristic of the TRIAD proteins of higher eukaryotes. Overexpression of Itt1p decreases the efficiency of translation termination, resulting in the readthrough of all three types of nonsense codons. Itt1p interacts in vitro with both eRFl and eRF3. Overexpression of eRFl, but not of eRF3, abolishes the nonsense suppressor effect of overexpressed Itt1p.
The data obtained demonstrate that Itt1p can modulate the efficiency of translation termination in yeast. This protein possesses a zinc finger domain characteristic of the TRIAD proteins of higher eukaryotes, and this is a first observation of such protein being involved in translation.
真核生物中翻译的终止由两个相互作用的多肽链释放因子eRFl和eRF3控制。eRFl识别无义密码子UAA、UAG和UGA,而eRF3以GTP和eRFl依赖的方式刺激多肽从核糖体释放。最近的研究表明,与这些释放因子相互作用的蛋白质可以调节无义密码子通读的效率。
我们分离出一个非必需的酵母基因,该基因以多拷贝状态存在时可导致无义突变的抑制。这个基因编码一种名为Itt1p的蛋白质,它具有高等真核生物TRIAD蛋白特有的锌指结构域。Itt1p的过表达降低了翻译终止的效率,导致所有三种类型的无义密码子通读。Itt1p在体外与eRFl和eRF3都相互作用。eRFl的过表达而非eRF3的过表达消除了过表达的Itt1p的无义抑制作用。
所获得的数据表明Itt1p可以调节酵母中翻译终止的效率。这种蛋白质具有高等真核生物TRIAD蛋白特有的锌指结构域,这是首次观察到此类蛋白质参与翻译过程。