Karniely Sharon, Pines Ophry
Department of Molecular Biology, Hebrew University Medical School, Jerusalem 91120, Israel.
EMBO Rep. 2005 May;6(5):420-5. doi: 10.1038/sj.embor.7400394.
It is well documented that single eukaryotic genes can give rise to proteins that are localized to several subcellular locations. This is achieved at the level of transcription, splicing and translation, and results in two or more translation products that either harbour or lack specific targeting signals. Nevertheless, the possibility of dual targeting of a single translation product has recently emerged. Here, we review cases of such dual targeting with emphasis on the mechanisms through which these phenomena occur. Proteins that harbour one signal, two separate signals or an overlapping ambiguous signal may follow dual distribution in the cell. The mechanism of dual targeting is driven by the competition or promiscuity of various molecular events. Protein folding, post-translational modification and protein-protein interaction are key players in this phenomenon.
有充分的文献记载,单个真核基因能够产生定位于多个亚细胞位置的蛋白质。这是在转录、剪接和翻译水平上实现的,会产生两种或更多种翻译产物,这些产物要么含有特定的靶向信号,要么缺乏特定的靶向信号。然而,单个翻译产物双重靶向的可能性最近才出现。在这里,我们回顾这种双重靶向的案例,重点关注这些现象发生的机制。含有一个信号、两个独立信号或重叠模糊信号的蛋白质可能在细胞中呈现双重分布。双重靶向的机制是由各种分子事件的竞争或混杂驱动的。蛋白质折叠、翻译后修饰和蛋白质 - 蛋白质相互作用是这一现象的关键因素。