{"title":"3 Processing of Yeast Cytoplasmic and Mitochondrial Precusor tRNAs","authors":"A. Hopper, N. Martin","doi":"10.1101/087969365.21B.99","DOIUrl":null,"url":null,"abstract":"I. INTRODUCTION The purpose of this chapter is to describe the processing of pre-tRNAs in yeast, integrating information on processing in the nucleus and mitochondria. Precursor tRNAs produced from nuclear genes and mitochondrial genes have the same general requirements: Various activities are needed to remove 5´leaders and 3´trailers, to add the CCA end, and to catalyze numerous base modifications (Fig. 1). In addition, a subset of nuclear pre-tRNAs have introns that must be removed, although no such activities are required for the biogenesis of any yeast mitochondria1 tRNA. Some yeast nuclear tRNA genes are transcribed together in dimeric pairs (Schmidt et al. 1980), and mitochondria1 tRNAs are transcribed with other tRNAs (Palleschi et al. 1984b; Martin et al. 1985b; Bardonne et al. 1987; Francisci et al. 1987), with ribosomal RNAs (Osinga et al. 1984; Palleschi et al. 1984a), with mRNAs (Miller et al. 1983; Zassenhaus et al. 1984), or with the RNasc P RNA (Shu and Martin 1991). Although these polycistronic transcripts are processed by a variety of activities, only those directly involved in tRNA recognition and processing are considered here. We have not attempted to review tRNA gene organization or transcription, as these topics have been covered elsewhere. The reader is referred to Guthrie and Abelson (1982) for a review of yeast nuclear tRNA genes, to Thuriaux and Sentenac (this volume) for a review of nuclear tRNA gene transcription, and to Tzagoloff and Myers (1986) for a review of mitochondria1 tRNA genes. In general, we have...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"1 1","pages":"99-141"},"PeriodicalIF":0.0000,"publicationDate":"2009-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969365.21B.99","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
I. INTRODUCTION The purpose of this chapter is to describe the processing of pre-tRNAs in yeast, integrating information on processing in the nucleus and mitochondria. Precursor tRNAs produced from nuclear genes and mitochondrial genes have the same general requirements: Various activities are needed to remove 5´leaders and 3´trailers, to add the CCA end, and to catalyze numerous base modifications (Fig. 1). In addition, a subset of nuclear pre-tRNAs have introns that must be removed, although no such activities are required for the biogenesis of any yeast mitochondria1 tRNA. Some yeast nuclear tRNA genes are transcribed together in dimeric pairs (Schmidt et al. 1980), and mitochondria1 tRNAs are transcribed with other tRNAs (Palleschi et al. 1984b; Martin et al. 1985b; Bardonne et al. 1987; Francisci et al. 1987), with ribosomal RNAs (Osinga et al. 1984; Palleschi et al. 1984a), with mRNAs (Miller et al. 1983; Zassenhaus et al. 1984), or with the RNasc P RNA (Shu and Martin 1991). Although these polycistronic transcripts are processed by a variety of activities, only those directly involved in tRNA recognition and processing are considered here. We have not attempted to review tRNA gene organization or transcription, as these topics have been covered elsewhere. The reader is referred to Guthrie and Abelson (1982) for a review of yeast nuclear tRNA genes, to Thuriaux and Sentenac (this volume) for a review of nuclear tRNA gene transcription, and to Tzagoloff and Myers (1986) for a review of mitochondria1 tRNA genes. In general, we have...
本章的目的是描述前trna在酵母中的加工过程,整合细胞核和线粒体中的加工信息。由核基因和线粒体基因产生的前体tRNA具有相同的一般要求:需要各种活性来去除5 '先导和3 '尾,添加CCA端,并催化许多碱基修饰(图1)。此外,一部分核前tRNA具有必须去除的内含子,尽管任何酵母线粒体tRNA的生物发生都不需要这种活性。一些酵母核tRNA基因以二聚体对的形式转录在一起(Schmidt et al. 1980),线粒体tRNA与其他tRNA一起转录(Palleschi et al. 1984b;Martin et al. 1985b;Bardonne et al. 1987;Francisci et al. 1987),核糖体rna (Osinga et al. 1984;Palleschi et al. 1984a)和mrna (Miller et al. 1983;Zassenhaus et al. 1984),或RNasc P RNA (Shu and Martin 1991)。虽然这些多顺反子转录本被多种活动加工,但这里只考虑直接参与tRNA识别和加工的转录本。我们没有试图回顾tRNA基因的组织或转录,因为这些主题已经在其他地方覆盖。读者可以参考Guthrie和Abelson(1982)对酵母核tRNA基因的综述,参考Thuriaux和Sentenac(本卷)对核tRNA基因转录的综述,参考Tzagoloff和Myers(1986)对线粒体tRNA基因的综述。总的来说,我们有……