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摆动肌苷tRNA修饰对于裂殖酵母在G(1)/S期和G(2)/M期转换过程中的细胞周期进程至关重要。

Wobble inosine tRNA modification is essential to cell cycle progression in G(1)/S and G(2)/M transitions in fission yeast.

作者信息

Tsutsumi Satoshi, Sugiura Reiko, Ma Yan, Tokuoka Hideki, Ohta Kazuki, Ohte Rieko, Noma Akiko, Suzuki Tsutomu, Kuno Takayoshi

机构信息

Division of Molecular Pharmacology and Pharmacogenomics, Department of Biochemistry and Molecular Biology, Graduate School of Medicine, Kobe University, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.

Laboratory of Molecular Pharmacogenomics, School of Pharmaceutical Sciences, Kinki University, Kowakae 3-4-1, Higashi-Osaka, 577-8502, Japan.

出版信息

J Biol Chem. 2007 Nov 16;282(46):33459-33465. doi: 10.1074/jbc.M706869200. Epub 2007 Sep 17.

Abstract

Inosine (I) at position 34 (wobble position) of tRNA is formed by the hydrolytic deamination of a genomically encoded adenosine (A). The enzyme catalyzing this reaction, termed tRNA A:34 deaminase, is the heterodimeric Tad2p/ADAT2.Tad3p/ADAT3 complex in eukaryotes. In budding yeast, deletion of each subunit is lethal, indicating that the wobble inosine tRNA modification is essential for viability; however, most of its physiological roles remain unknown. To identify novel cell cycle mutants in fission yeast, we isolated the tad3-1 mutant that is allelic to the tad3(+) gene encoding a homolog of budding yeast Tad3p. Interestingly, the tad3-1 mutant cells principally exhibited cell cycle-specific phenotype, namely temperature-sensitive and irreversible cell cycle arrest both in G(1) and G(2). Further analyses revealed that in the tad3-1 mutant cells, the S257N mutation that occurred in the catalytically inactive Tad3 subunit affected its association with catalytically active Tad2 subunit, leading to an impairment in the A to I conversion at position 34 of tRNA. In tad3-1 mutant cells, the overexpression of the tad3(+) gene completely suppressed the decreased tRNA inosine content. Notably, the overexpression of the tad2(+) gene partially suppressed the temperature-sensitive phenotype and the decreased tRNA inosine content, indicating that the tad3-1 mutant phenotype is because of the insufficient I(34) formation of tRNA. These results suggest that the wobble inosine tRNA modification is essential for cell cycle progression in the G(1)/S and G(2)/M transitions in fission yeast.

摘要

转运RNA(tRNA)第34位(摆动位置)的肌苷(I)由基因组编码的腺苷(A)经水解脱氨形成。催化此反应的酶称为tRNA A:34脱氨酶,在真核生物中是异二聚体Tad2p/ADAT2.Tad3p/ADAT3复合物。在芽殖酵母中,每个亚基的缺失都是致死的,这表明摆动肌苷tRNA修饰对细胞存活至关重要;然而,其大多数生理作用仍不清楚。为了在裂殖酵母中鉴定新的细胞周期突变体,我们分离出了tad3-1突变体,它与编码芽殖酵母Tad3p同源物的tad3(+)基因等位。有趣的是,tad3-1突变体细胞主要表现出细胞周期特异性表型,即在G(1)期和G(2)期均对温度敏感且不可逆的细胞周期停滞。进一步分析表明,在tad3-1突变体细胞中,催化无活性的Tad3亚基中发生的S257N突变影响了它与催化活性Tad2亚基的结合,导致tRNA第34位的A到I转换受损。在tad3-1突变体细胞中,tad3(+)基因的过表达完全抑制了tRNA肌苷含量的降低。值得注意的是,tad2(+)基因的过表达部分抑制了温度敏感表型和tRNA肌苷含量的降低,表明tad3-1突变体表型是由于tRNA的I(34)形成不足。这些结果表明,摆动肌苷tRNA修饰对于裂殖酵母在G(1)/S和G(2)/M转换过程中的细胞周期进展至关重要。

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