Müller P P, Reif M K, Zonghou S, Sengstag C, Mason T L, Fox T D
J Mol Biol. 1984 Jun 5;175(4):431-52. doi: 10.1016/0022-2836(84)90178-5.
The nuclear amber mutation, pet494-1, specifically blocks the accumulation of the product of the mitochondrial gene oxi2, cytochrome oxidase subunit III. The pet494-1 mutation does not prevent transcription of the mitochondrial gene since RNA--gel blot hybridizations showed that mutant cells contain normal amounts of an oxi2 transcript, indistinguishable in size from wild-type. A mitochondrial mutation that partially suppresses the nuclear mutation was isolated. The "mitochondrial revertant" behaved as though it contained two different mitochondrial DNAs: one rho+, the other rho-. The suppressor mutation is carried on the rho- mitochondrial DNA and is apparently the result of a gene fusion between oxi2 and another mitochondrial gene, oxi3. This gene rearrangement replaced the normal 5'-non-translated sequence of oxi2 with a portion of the open reading frame of the second intron of oxi3. Novel transcripts of the rearranged gene, containing oxi3 sequences upstream from oxi2 were detected in the mitochondrial revertant. The strain accumulated an electrophoretically variant form of cytochrome oxidase subunit III, probably translated from a new initiation codon. The data are consistent with models in which the PET494 protein acts within the mitochondria to specifically promote the translation of the oxi2 messenger RNA.
核琥珀突变体pet494-1特异性地阻断了线粒体基因oxi2(细胞色素氧化酶亚基III)产物的积累。pet494-1突变并不阻止线粒体基因的转录,因为RNA-凝胶印迹杂交显示突变细胞含有正常量的oxi2转录本,其大小与野生型无法区分。分离出了一个部分抑制核突变的线粒体突变。“线粒体回复突变体”的行为就好像它含有两种不同的线粒体DNA:一种是ρ⁺型,另一种是ρ⁻型。抑制突变位于ρ⁻线粒体DNA上,显然是oxi2和另一个线粒体基因oxi3之间基因融合的结果。这种基因重排用oxi3第二个内含子的一部分开放阅读框取代了oxi2正常的5'-非翻译序列。在这个线粒体回复突变体中检测到了重排基因的新转录本,其在oxi2上游含有oxi3序列。该菌株积累了一种细胞色素氧化酶亚基III的电泳变异形式,可能是从一个新的起始密码子翻译而来。这些数据与PET494蛋白在线粒体内起作用以特异性促进oxi2信使RNA翻译的模型一致。