Kreike J, Schulze M, Ahne F, Lang B F
Institut für Genetik und Mikrobiologie, Universität München, FRG.
EMBO J. 1987 Jul;6(7):2123-9. doi: 10.1002/j.1460-2075.1987.tb02479.x.
We have cloned a 1.6-kb fragment of yeast nuclear DNA, which complements pet- mutant MK3 (mrs1). This mutant was shown to be defective in mitochondrial RNA splicing: the excision of intron 3 from the mitochondrial COB pre-RNA is blocked. The DNA sequence of the nuclear DNA fragment revealed two open reading frames (ORF1 with 1092 bp; ORF2 with 735 bp) on opposite strands, which overlap by 656 bp. As shown by in vitro mutagenesis, ORF1, but not ORF2, is responsible for complementation of the splice defect. Hence, ORF1 represents the nuclear MRS1 gene. Disruption of the gene (both ORFs) in the chromosomal DNA of the respiratory competent yeast strain DBY747 (long form COB gene) leads to a stable pet- phenotype and to the accumulation of the same mitochondrial RNA precursors as in strain MK3. The amino acid sequence of the putative ORF1 product does not exhibit any homology with other known proteins, except for a small region of homology with the gene product of another nuclear yeast gene involved in mitochondrial RNA splicing, CBP2. The function of the MRS1 (ORF1) gene in mitochondrial RNA splicing and the significance of the overlapping ORFs in this gene are discussed.
我们克隆了一段1.6kb的酵母核DNA片段,它能互补pet-突变体MK3(mrs1)。该突变体被证明在线粒体RNA剪接方面存在缺陷:线粒体COB前体RNA中内含子3的切除受阻。核DNA片段的DNA序列显示,在相反的两条链上有两个开放阅读框(ORF1为1092bp;ORF2为735bp),它们重叠656bp。体外诱变实验表明,是ORF1而非ORF2负责互补剪接缺陷。因此,ORF1代表核MRS1基因。在呼吸正常的酵母菌株DBY747(长形式COB基因)的染色体DNA中破坏该基因(两个ORF)会导致稳定的pet-表型,并积累与MK3菌株中相同的线粒体RNA前体。假定的ORF1产物的氨基酸序列与其他已知蛋白质没有任何同源性,除了与另一个参与线粒体RNA剪接的酵母核基因CBP2的基因产物有一小段同源区域。本文讨论了MRS1(ORF1)基因在线粒体RNA剪接中的功能以及该基因中重叠ORF的意义。