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线粒体内含子中的关键序列:氧化酶基因“细胞色素b样”内含子的顺式显性突变

Critical sequences within mitochondrial introns: cis-dominant mutations of the "cytochrome-b-like" intron of the oxidase gene.

作者信息

Netter P, Jacq C, Carignani G, Slonimski P P

出版信息

Cell. 1982 Apr;28(4):733-8. doi: 10.1016/0092-8674(82)90052-6.

Abstract

We have established the DNA sequence of two cis-dominant mutations located in the fourth intron, a14, of the yeast mitochondrial gene oxi3. These mutations prevent the synthesis of subunit I of cytochrome oxidase. Both mutations affect a very short DNA sequence located several hundred base pairs from the intron-exon junctions. An identical sequence is found in the cob-box gene; and this sequence is critical for the excision of the cytochrome b intron. Our interpretation is that this short sequence represents a common signal that must be recognized by the box7-encoded mRNA maturase, in conjunction with the mitochondrial ribosome, to splice out the introns in the two nonhomologous genes, cob-box and oxi3.

摘要

我们已经确定了酵母线粒体基因oxi3的第四个内含子a14中两个顺式显性突变的DNA序列。这些突变阻止了细胞色素氧化酶亚基I的合成。两个突变都影响了一个非常短的DNA序列,该序列位于距离内含子-外显子连接处几百个碱基对的位置。在cob-box基因中发现了相同的序列;并且这个序列对于细胞色素b内含子的切除至关重要。我们的解释是,这个短序列代表了一个共同的信号,必须被box7编码的mRNA成熟酶与线粒体核糖体一起识别,以便切除两个非同源基因cob-box和oxi3中的内含子。

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