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酿酒酵母中TRM1基因座的分离与鉴定,该基因对于线粒体和细胞质tRNA的N2,N2-二甲基鸟苷修饰至关重要。

Isolation and characterization of the TRM1 locus, a gene essential for the N2,N2-dimethylguanosine modification of both mitochondrial and cytoplasmic tRNA in Saccharomyces cerevisiae.

作者信息

Ellis S R, Morales M J, Li J M, Hopper A K, Martin N C

出版信息

J Biol Chem. 1986 Jul 25;261(21):9703-9.

PMID:2426253
Abstract

The trm1 mutation of Saccharomyces cerevisiae is a single nuclear mutation that affects a specific base modification of both cytoplasmic and mitochondrial tRNA. Transfer RNA isolated from trm1 cells lacks the modified base N2,N2-dimethylguanosine, and extracts from these cells do not have detectable N2,N2-dimethylguanosine-specific tRNA methyltransferase activity. As part of our efforts to determine how this mutation affects enzyme activities in two different cellular compartments we have isolated the TRM1 locus by genetic complementation. The TRM1 locus restores the N2,N2-dimethylguanosine modification to both cytoplasmic and mitochondrial tRNA in trm1 cells. An open reading frame in this TRM1 gene is essential for complementation of the trm1 phenotype. Expression of this open reading frame in Escherichia coli converts the organism from one that neither makes N2,N2-dimethylguanosine nor has N2,N2-dimethylguanosine-specific tRNA methyltransferase activity into one that does. This result suggests that the TRM1 locus is the structural gene for the tRNA modification enzyme and that both nuclear/cytoplasmic and mitochondrial forms of the methyltransferase are produced from the same gene.

摘要

酿酒酵母的trm1突变是一种单核突变,它影响细胞质和线粒体tRNA的特定碱基修饰。从trm1细胞中分离出的转运RNA缺乏修饰碱基N2,N2 - 二甲基鸟苷,并且这些细胞的提取物没有可检测到的N2,N2 - 二甲基鸟苷特异性tRNA甲基转移酶活性。作为我们确定该突变如何影响两个不同细胞区室中酶活性的工作的一部分,我们通过基因互补分离出了TRM1基因座。TRM1基因座可恢复trm1细胞中细胞质和线粒体tRNA的N2,N2 - 二甲基鸟苷修饰。该TRM1基因中的一个开放阅读框对于trm1表型的互补至关重要。此开放阅读框在大肠杆菌中的表达将该生物体从既不产生N2,N2 - 二甲基鸟苷也没有N2,N2 - 二甲基鸟苷特异性tRNA甲基转移酶活性的生物体转变为具有这些活性的生物体。这一结果表明,TRM1基因座是tRNA修饰酶的结构基因,并且甲基转移酶的核/细胞质形式和线粒体形式均由同一基因产生。

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