Esser K, Pratje E, Michaelis G
Botanisches Institut der Universität Düsseldorf, Germany.
Mol Gen Genet. 1996 Sep 25;252(4):437-45. doi: 10.1007/BF02173009.
IMP1 encodes a subunit of the mitochondrial inner membrane peptidase responsible for the proteolytic processing of cytochrome oxidase subunit 2 (Cox2) and cytochrome b2 (Cytb2). The molecular defect in an imp1 mutation and the characterisation of a high-copy-number suppressor is described. A deletion of the suppressor region causes respiration deficiency. The DNA sequence revealed three very small overlapping ORFs. Constructs which carried termination codons within the ORFs or lacked ATG initiation codons still retained complementing activity on a high-copy-number plasmid. Nevertheless, the possibility that the suppressor acts at DNA or RNA level could be excluded. Subcloning of the ORFs, complementation analysis in low-copy-number plasmids and transcript mapping identified the 222 bp ORF as the suppressor gene designated SOM1. The SOM1 gene is transcribed into a 375 bp polyadenylated RNA and the deduced amino acid sequence predicts a small protein of 8.4 kDa with no significant sequence similarity to known proteins. In the som1 deletion mutant, proteolytic processing of the Cox2 precursor is prevented and Cytb2 is strongly reduced. SOM1 represents a new small gene which encodes a novel factor that is essential for the correct function of the Imp1 peptidase and/or the protein sorting machinery.
IMP1编码线粒体内膜肽酶的一个亚基,该肽酶负责细胞色素氧化酶亚基2(Cox2)和细胞色素b2(Cytb2)的蛋白水解加工。本文描述了imp1突变中的分子缺陷以及高拷贝数抑制子的特征。抑制子区域的缺失导致呼吸缺陷。DNA序列显示有三个非常小的重叠开放阅读框(ORF)。在开放阅读框内带有终止密码子或缺少ATG起始密码子的构建体在高拷贝数质粒上仍保留互补活性。然而,可以排除抑制子在DNA或RNA水平起作用的可能性。开放阅读框的亚克隆、低拷贝数质粒中的互补分析以及转录本定位确定了222 bp的开放阅读框为名为SOM1的抑制基因。SOM1基因转录成一个375 bp的多聚腺苷酸化RNA,推导的氨基酸序列预测出一个8.4 kDa的小蛋白,与已知蛋白没有明显的序列相似性。在som1缺失突变体中,Cox2前体的蛋白水解加工被阻止,Cytb2显著减少。SOM1代表一个新的小基因,它编码一种对Imp1肽酶和/或蛋白质分选机制的正确功能至关重要的新因子。