Schuster W, Wissinger B, Unseld M, Brennicke A
Institut für Genbiologische Forschung, Berlin, FRG.
EMBO J. 1990 Jan;9(1):263-9. doi: 10.1002/j.1460-2075.1990.tb08104.x.
A number of cytosines are altered to be recognized as uridines in transcripts of the nad3 locus in mitochondria of the higher plant Oenothera. Such nucleotide modifications can be found at 16 different sites within the nad3 coding region. Most of these alterations in the mRNA sequence change codon identities to specify amino acids better conserved in evolution. Individual cDNA clones differ in their degree of editing at five nucleotide positions, three of which are silent, while two lead to codon alterations specifying different amino acids. None of the cDNA clones analysed is maximally edited at all possible sites, suggesting slow processing or lowered stringency of editing at these nucleotides. Differentially edited transcripts could be editing intermediates or could code for differing polypeptides. Two edited nucleotides in an open reading frame located upstream of nad3 change two amino acids in the deduced polypeptide. Part of the well-conserved ribosomal protein gene rps12 also encoded downstream of nad3 in other plants, is lost in Oenothera mitochondria by recombination events. The functional rps12 protein must be imported from the cytoplasm since the deleted sequences of this gene are not found in the Oenothera mitochondrial genome. The pseudogene sequence is not edited at any nucleotide position.
在高等植物月见草线粒体中,nad3基因座转录本中的许多胞嘧啶被改变为尿嘧啶。在nad3编码区内的16个不同位点可发现这种核苷酸修饰。mRNA序列中的这些改变大多会改变密码子的特性,以指定在进化过程中更保守的氨基酸。各个cDNA克隆在五个核苷酸位置的编辑程度不同,其中三个是沉默的,而另外两个会导致密码子改变,指定不同的氨基酸。分析的所有cDNA克隆在所有可能的位点都没有达到最大程度的编辑,这表明这些核苷酸的加工过程缓慢或编辑的严格性降低。差异编辑的转录本可能是编辑中间体,也可能编码不同的多肽。nad3上游一个开放阅读框中的两个编辑核苷酸改变了推导多肽中的两个氨基酸。在其他植物中,nad3下游还编码的部分保守核糖体蛋白基因rps12,在月见草线粒体中因重组事件而丢失。功能性rps12蛋白必须从细胞质中导入,因为该基因的缺失序列在月见草线粒体基因组中未被发现。假基因序列在任何核苷酸位置都未被编辑。