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细胞质和线粒体转运RNA修饰缺陷由单核基因突变引起。

Defects in modification of cytoplasmic and mitochondrial transfer RNAs are caused by single nuclear mutations.

作者信息

Hopper A K, Furukawa A H, Pham H D, Martin N C

出版信息

Cell. 1982 Mar;28(3):543-50. doi: 10.1016/0092-8674(82)90209-4.

Abstract

Many nucleus-encoded mitochondrial enzymes differ in physical and chemical properties from analogous cytoplasmic enzymes, and it is therefore generally assumed that different genes encode analogous mitochondrial and cytoplasmic enzymes. However, our genetic studies show that for at least two different tRNA modifications, mutations in nuclear genes affect cytoplasmic as well as mitochondrial tRNAs. These studies utilize two yeast genes: TRM1 and TRM2. trm1 cells do not have the enzyme activity necessary to methylate guanosine to N2,N2-dimethylguanosine. trm2 is a new mutation that we describe here. trm2 cells are deficient in tRNA-(uridine-5)methyltransferase, and hence contain tRNA lacking 5-methyluridine or ribothymidine. Other than lacking 5-methyluridine trm2 cells have no obvious physiological defect. These studies also show that the N2,N2-dimethylguanosine and 5-methyluridine modifications are not added to tRNA in an obligatory order, and that 5-methyluridine is not required for removal of intervening sequences from precursor tRNA.

摘要

许多由细胞核编码的线粒体酶在物理和化学性质上与类似的细胞质酶不同,因此通常认为不同的基因编码类似的线粒体酶和细胞质酶。然而,我们的遗传学研究表明,至少对于两种不同的tRNA修饰而言,核基因中的突变会影响细胞质tRNA和线粒体tRNA。这些研究利用了两个酵母基因:TRM1和TRM2。trm1细胞不具备将鸟苷甲基化为N2,N2-二甲基鸟苷所需的酶活性。trm2是我们在此描述的一个新突变。trm2细胞缺乏tRNA-(尿苷-5)甲基转移酶,因此含有缺乏5-甲基尿苷或核糖胸腺嘧啶的tRNA。除了缺乏5-甲基尿苷外,trm2细胞没有明显的生理缺陷。这些研究还表明,N2,N2-二甲基鸟苷和5-甲基尿苷修饰并非按固定顺序添加到tRNA上,并且从前体tRNA中去除间隔序列并不需要5-甲基尿苷。

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