ARC Centre of Excellence in Plant Energy Biology, MCS Building M316, University of Western Australia, 35 Stirling Highway, Crawley 6009, Western Australia, Australia.
Mol Plant. 2009 Nov;2(6):1310-24. doi: 10.1093/mp/ssp053. Epub 2009 Jul 24.
To obtain a global overview of how mitochondria respond to stress, we aimed to define the plant mitochondrial stress response (MSR). By combining a set of 1196 Arabidopsis thaliana genes that putatively encode mitochondrial proteins with 16 microarray experiments on stress-related conditions, 45 nuclear encoded genes were defined as widely stress-responsive. Using green fluorescent protein (GFP) fusion assays, the mitochondrial targeting of a large number of these proteins was tested, confirming in total 26 proteins as mitochondrially targeted. Several of these proteins were observed to be dual targeted to mitochondria and plastids, including the small heat shock proteins sHSP23.5 and sHSP23.6. In addition to the well defined stress components of mitochondria, such as alternative oxidases, nicotinamide adenine dinucleotide (NAD(P)H) dehydrogenases, and heat shock proteins, a variety of other proteins, many with unknown function, were identified. The mitochondrial carrier protein family was over-represented in the stress-responsive genes, suggesting that stress induces altered needs for metabolite transport across the mitochondrial inner membrane. Although the genes encoding many of these proteins contain common cis-acting regulatory elements, it was apparent that a number of distinct regulatory processes or signals likely triggered the MSR. Therefore, these genes provide new model systems to study mitochondrial retrograde regulation, in addition to the widely used alternative oxidase model. Additionally, as changes in proteins responsive to stress did not correlate well with changes at a transcript level, it suggests that post-transcriptional mechanisms also play an important role in defining the MSR.
为了全面了解线粒体对胁迫的反应,我们旨在定义植物线粒体应激反应(MSR)。通过将一组 1196 个拟编码线粒体蛋白的拟南芥基因与 16 个与应激相关条件的微阵列实验相结合,鉴定出 45 个核编码基因作为广泛应激反应基因。通过绿色荧光蛋白(GFP)融合测定,对这些蛋白中的大量蛋白进行了线粒体靶向测试,总共确认了 26 个蛋白为线粒体靶向。观察到其中一些蛋白双重靶向线粒体和质体,包括小热休克蛋白 sHSP23.5 和 sHSP23.6。除了线粒体的明确应激成分,如交替氧化酶、烟酰胺腺嘌呤二核苷酸(NAD(P)H)脱氢酶和热休克蛋白外,还鉴定出了许多其他蛋白,其中许多蛋白具有未知功能。在线粒体应激反应基因中,线粒体载体蛋白家族的含量过高,这表明应激诱导了代谢物跨线粒体内膜运输的改变需求。尽管编码这些蛋白的基因包含常见的顺式作用调节元件,但显然有许多不同的调节过程或信号可能触发了 MSR。因此,除了广泛使用的交替氧化酶模型外,这些基因还为研究线粒体逆行调节提供了新的模型系统。此外,由于对胁迫有反应的蛋白质的变化与转录水平的变化相关性较差,这表明转录后机制也在定义 MSR 中发挥重要作用。