Department of Microbiology Molecular Genetics, IMRIC, Hebrew University of Jerusalem, Jerusalem, Israel.
Proteomics. 2011 Dec;11(23):4468-76. doi: 10.1002/pmic.201100199. Epub 2011 Oct 28.
There are a growing number of examples of identical or almost identical proteins, which are localized to two (or more) separate compartments, a phenomenon that is termed protein dual localization, dual distribution or dual targeting. We previously divided a reference set of known yeast mitochondrial proteins into two groups, suggested to be dual localized or exclusive mitochondrial proteins. Here we examined this evaluation by screening 320 mitochondrial gene products for dual targeting, using the α-complementation assay. The analysis of the results of this experimentally independent screen supports our previous evaluation that dual localized mitochondrial proteins constitute a subgroup of mitochondrial proteins with distinctive properties. These proteins are characterized by a lower probability of mitochondrial localization (MitoProtII score), a lower net charge and are enriched for proteins with a weaker mitochondrial targeting sequence. Conversely, mRNAs of exclusive mitochondrial proteins are enriched in polysomes associated with mitochondria. Based on the discovery of more than 60 new gene products that are now assumed to be dual targeted, we have updated an annotation list of dual-targeted proteins. We currently estimate that more than a third of the mitochondrial proteome is dual targeted, and suggest that this abundant dual targeting presents an evolutionary advantage.
越来越多的例子表明,蛋白质可以定位于两个(或更多)不同的隔室,这种现象被称为蛋白质双重定位、双重分布或双重靶向。我们之前将一组已知的酵母线粒体蛋白分为两组,这两组被认为是双重定位或仅定位于线粒体的蛋白。在这里,我们使用α互补测定法,通过筛选 320 种线粒体基因产物来检测双重靶向,以检验这种评估。对这一独立实验结果的分析支持我们之前的评估,即双重定位的线粒体蛋白构成了具有独特特性的线粒体蛋白亚组。这些蛋白的特征是线粒体定位的可能性较低(MitoProtII 评分)、净电荷较低,并且富含线粒体靶向序列较弱的蛋白。相反,仅定位于线粒体的蛋白的 mRNA 在与线粒体相关的多核糖体中富集。基于发现了 60 多种新的双重靶向的基因产物,我们更新了双重靶向蛋白的注释列表。我们目前估计,线粒体蛋白质组的三分之一以上是双重靶向的,并且表明这种丰富的双重靶向具有进化优势。