Carignani G, Netter P, Bergantino E, Robineau S
Istituto di Chimica Biologica dell'Università di Padova, Italy.
Curr Genet. 1986;11(1):55-63. doi: 10.1007/BF00389426.
We have studied the splicing pathway leading to the synthesis of cytochrome oxidase subunit I (COX I) mRNA, by analysing the transcription pattern of several oxi3- splicing deficient mutants located in the first four introns of the gene. The four introns contain long open reading frames (ORFs) in phase with the upstream exons. All the mutations block the excision of the mutated intervening sequence (IVS) from the pre-mRNA, and accumulate characteristic novel polypeptides of sizes which could correspond to the translation products of the intron's ORF. Most of the mutations do not affect the splicing of the following intervening sequences; only in the case of mutations in the aI1 intron is a polar effect observed on the splicing of the second intron, aI2. Our results indicate that the splicing of these two intervening sequences which both belong to the class II of introns described by Michel et al. (1982), is controlled by the activity of the maturases encoded by their respective ORFs and that the translation of the aI2 maturase depends on the previous excision of aI1 IVS. (Moreover, the aI1 maturase, which accumulates in some mutants, can efficiently splice aI2 IVS when the translation of the latter's proper maturase cannot occur).
我们通过分析位于该基因前四个内含子中的几个oxi3剪接缺陷突变体的转录模式,研究了导致细胞色素氧化酶亚基I(COX I)mRNA合成的剪接途径。这四个内含子含有与上游外显子相位一致的长开放阅读框(ORF)。所有突变均阻止了前体mRNA中突变的间隔序列(IVS)的切除,并积累了大小特征性的新型多肽,其大小可能与内含子ORF的翻译产物相对应。大多数突变不影响后续间隔序列的剪接;仅在aI1内含子发生突变的情况下,才观察到对第二个内含子aI2剪接的极性效应。我们的结果表明,这两个均属于Michel等人(1982年)描述的II类内含子的间隔序列的剪接,受其各自ORF编码的成熟酶活性的控制,并且aI2成熟酶的翻译取决于aI1 IVS的先前切除。(此外,在一些突变体中积累的aI1成熟酶,当后者自身的成熟酶无法进行翻译时,可以有效地剪接aI2 IVS)。