Huang Shaobai, Taylor Nicolas L, Whelan James, Millar A Harvey
Australian Research Council Centre of Excellence in Plant Energy Biology, M316, University of Western Australia, Crawley, Western Australia 6009, Australia.
Plant Physiol. 2009 Jul;150(3):1272-85. doi: 10.1104/pp.109.137885. Epub 2009 May 27.
Mitochondrial protein import is a complex multistep process from synthesis of proteins in the cytosol, recognition by receptors on the organelle surface, to translocation across one or both mitochondrial membranes and assembly after removal of the targeting signal, referred to as a presequence. In plants, import has to further discriminate between mitochondria and chloroplasts. In this study, we determined the precise cleavage sites in the presequences for Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) mitochondrial proteins using mass spectrometry by comparing the precursor sequences with experimental evidence of the amino-terminal peptide from mature proteins. We validated this method by assessments of false-positive rates and comparisons with previous available data using Edman degradation. In total, the cleavable presequences of 62 proteins from Arabidopsis and 52 proteins from rice mitochondria were determined. None of these proteins contained amino-terminal acetylation, in contrast to recent findings for chloroplast stromal proteins. Furthermore, the classical matrix glutamate dehydrogenase was detected with intact and amino-terminal acetylated sequences, indicating that it is imported into mitochondria without a cleavable targeting signal. Arabidopsis and rice mitochondrial presequences had similar isoelectric points, hydrophobicity, and the predicted ability to form an amphiphilic alpha-helix at the amino-terminal region of the presequence, but variations in length, amino acid composition, and cleavage motifs for mitochondrial processing peptidase were observed. A combination of lower hydrophobicity and start point of the amino-terminal alpha-helix in mitochondrial presequences in both Arabidopsis and rice distinguished them (98%) from Arabidopsis chloroplast stroma transit peptides. Both Arabidopsis and rice mitochondrial cleavage sites could be grouped into three classes, with conserved -3R (class II) and -2R (class I) or without any conserved (class III) arginines. Class II was dominant in both Arabidopsis and rice (55%-58%), but in rice sequences there was much less frequently a phenylalanine (F) in the -1 position of the cleavage site than in Arabidopsis sequences. Our data also suggest a novel cleavage motif of (F/Y) downward arrow(S/A) in plant class III sequences.
线粒体蛋白输入是一个复杂的多步骤过程,从胞质溶胶中蛋白质的合成开始,被细胞器表面的受体识别,到穿过一层或两层线粒体膜进行转运,并在去除称为前导序列的靶向信号后进行组装。在植物中,蛋白输入还必须进一步区分线粒体和叶绿体。在本研究中,我们通过质谱法,将前体序列与成熟蛋白氨基末端肽段的实验证据进行比较,确定了拟南芥和水稻线粒体蛋白前导序列中的精确切割位点。我们通过评估假阳性率以及与先前使用埃德曼降解法获得的数据进行比较,验证了该方法。总共确定了拟南芥62种蛋白质和水稻线粒体52种蛋白质的可切割前导序列。与叶绿体基质蛋白的最新研究结果相反,这些蛋白质均未含有氨基末端乙酰化修饰。此外,经典的线粒体基质谷氨酸脱氢酶被检测到具有完整且氨基末端乙酰化的序列,这表明它在没有可切割靶向信号的情况下被输入到线粒体中。拟南芥和水稻线粒体前导序列在前导序列氨基末端区域具有相似的等电点、疏水性以及预测形成两亲性α螺旋的能力,但在前导序列长度、氨基酸组成以及线粒体加工肽酶的切割基序方面存在差异。拟南芥和水稻线粒体前导序列较低的疏水性以及氨基末端α螺旋的起始点,将它们与拟南芥叶绿体基质转运肽区分开来(98%)。拟南芥和水稻线粒体的切割位点均可分为三类,具有保守的-3R(II类)和-2R(I类)或没有任何保守的精氨酸(III类)。II类在拟南芥和水稻中均占主导地位(55%-58%),但在水稻序列中,切割位点-1位置的苯丙氨酸(F)出现频率远低于拟南芥序列。我们的数据还表明,植物III类序列中存在一种新的切割基序(F/Y)↓(S/A)。