Dieckmann C L, Homison G, Tzagoloff A
J Biol Chem. 1984 Apr 25;259(8):4732-8.
A nuclear gene (CBP1) of Saccharomyces cerevisiae involved in 5' end processing of the cytochrome b pre-mRNA has been cloned and sequenced. The gene was originally selected by transformation of cbp1 mutants with a recombinant plasmid bank of random fragments of yeast nuclear DNA ligated to a plasmid vector with autonomous replicative function in yeast. The recombinant plasmid pG60/T10 with a nuclear DNA insert of 6.7 kilobase pairs (kb) was used to construct a new plasmid pool with the CBP1 gene on smaller fragments of nuclear DNA. A number of subclones have been isolated with plasmids carrying inserts of 2.4 to 6.1 kb. The plasmid designated pG60/T31 confers respiratory competency to cbp1 mutants and restores their ability to synthesize mature cytochrome b mRNA. The pG60/T31 plasmid has a nuclear DNA insert of 2.4 kb. The sequence of the cloned fragment reveals only one open reading frame capable of coding for a protein. The reading frame is 1962 nucleotides long and codes for a basic polypeptide with a molecular weight of 76,140. A transcript of a size commensurate with the length of the gene has been detected in wild type yeast.
酿酒酵母中一个参与细胞色素b前体mRNA 5'端加工的核基因(CBP1)已被克隆和测序。该基因最初是通过用酵母核DNA随机片段的重组质粒文库转化cbp1突变体来筛选的,这些片段与在酵母中具有自主复制功能的质粒载体相连。带有6.7千碱基对(kb)核DNA插入片段的重组质粒pG60/T10被用于构建一个新的质粒文库,其中CBP1基因位于核DNA的较小片段上。已经分离出许多亚克隆,其质粒携带2.4至6.1 kb的插入片段。命名为pG60/T31的质粒赋予cbp1突变体呼吸能力,并恢复其合成成熟细胞色素b mRNA的能力。pG60/T31质粒有一个2.4 kb的核DNA插入片段。克隆片段的序列仅显示一个能够编码蛋白质的开放阅读框。该阅读框长1962个核苷酸,编码一个分子量为76,140的碱性多肽。在野生型酵母中已检测到与基因长度相当的转录本。