Murayama Seiji, Handa Hirokazu
Research Team for Crop Cold Tolerance, National Agricultural Research Center for Hokkaido Region, 1 Hitsuji-ga-oka, Sapporo 062-8555, Japan.
Planta. 2007 Apr;225(5):1193-203. doi: 10.1007/s00425-006-0430-x. Epub 2006 Nov 4.
Two cDNA clones (OsNIN1 and OsNIN3) encoding an alkaline/neutral invertase localized in organelles were identified from rice. The deduced amino acid sequences of these cDNA clones showed high homology to other plant alkaline/neutral invertases. Semi-quantitative reverse transcription polymerase chain reaction revealed that the expression of OsNIN1 was constitutive and independent of organ difference, although its expression level was low. Analyses using five types of web software for the prediction of protein localization in the cell, Predotar, PSORT, Mitoprot, TargetP, and ChloroP, strongly supported the possibility that OsNIN1 is transported into the mitochondria and that OsNIN3 is transported into plastids. Transient expression of fusion proteins combining the amino terminal region of these two proteins with sGFP demonstrated that N-OsNIN1::GFP and N-OsNIN3::GFP fusion proteins were transported into the mitochondria and plastids, respectively. We expressed the OsNIN1 protein in vitro and revealed that the translated protein had an invertase activity. These results clearly indicate that some of alkaline/neutral invertases are located in plant organelles, mitochondria and plastids, and that they might have a novel physiological function in plant organelles.
从水稻中鉴定出两个编码定位于细胞器的碱性/中性转化酶的cDNA克隆(OsNIN1和OsNIN3)。这些cDNA克隆推导的氨基酸序列与其他植物碱性/中性转化酶具有高度同源性。半定量逆转录聚合酶链反应显示,OsNIN1的表达是组成型的,且与器官差异无关,尽管其表达水平较低。使用Predotar、PSORT、Mitoprot、TargetP和ChloroP这五种用于预测细胞中蛋白质定位的网络软件进行分析,有力地支持了OsNIN1被转运到线粒体以及OsNIN3被转运到质体的可能性。将这两种蛋白质的氨基末端区域与sGFP结合的融合蛋白的瞬时表达表明,N-OsNIN1::GFP和N-OsNIN3::GFP融合蛋白分别被转运到线粒体和质体中。我们在体外表达了OsNIN1蛋白,并发现翻译后的蛋白具有转化酶活性。这些结果清楚地表明,一些碱性/中性转化酶位于植物细胞器、线粒体和质体中,并且它们可能在植物细胞器中具有新的生理功能。