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盐碱胁迫下羽扇豆胚轴。II. 线粒体蛋白质组反应。

Lupine embryo axes under salinity stress. II. Mitochondrial proteome response.

作者信息

Wojtyla Łukasz, Kosmala Arkadiusz, Garnczarska Małgorzata

机构信息

Department of Plant Physiology, Faculty of Biology, Adam Mickiewicz University, ul. Umultowska 89, 61-614 Poznań, Poland.

Laboratory of Cytogenetics, Institute of Plant Genetics, Polish Academy of Sciences, ul. Strzeszyńska 34, 60-479 Poznań, Poland.

出版信息

Acta Physiol Plant. 2013;35(8):2383-2392. doi: 10.1007/s11738-013-1273-2. Epub 2013 Apr 3.

Abstract

Germination is the first step of plant growth in plant life cycle. An embryonic radicle protruding the seed coat is the first part of plant which has direct contact with external environment including salt-affected soil. In embryo axes, mitochondria are the main energy producer. To understand better salinity impact on mitochondria functioning, this study was focused on the effect of NaCl stress onto mitochondria proteome. Mitochondria were isolated from yellow lupine ( L. 'Mister') embryo axes cultured in vitro for 12 h with 250 and 500 mM NaCl. Two-dimensional gel electrophoresis of mitochondrial proteins isolated from NaCl-treated axes demonstrated significant changes in proteins abundances as a response to salinity treatment. Twenty-one spots showing significant changes in protein expression profiles both under 250 and 500 mM NaCl treatment were selected for tandem mass spectrometry identification. This approach revealed proteins associated with different metabolic processes that represent enzymes of tricarboxylic acid cycle, mitochondrial electron transport chain, enzymes and proteins involved in mitochondria biogenesis and stresses response. Among proteins involved in mitochondria biogenesis, mitochondrial import inner membrane translocase, subunit Tim17/22, mitochondrial-processing peptidase subunit alpha-1, mitochondrial elongation factor Tu and chaperonins CPN60 were revealed. Finally, formate dehydrogenase 1 was found to accumulate in lupine embryo axes mitochondria under salinity. The functions of identified proteins are discussed in relation to salinity stress response, including salinity-induced PCD.

摘要

发芽是植物生命周期中植物生长的第一步。胚根突出种皮是植物与包括盐渍土壤在内的外部环境直接接触的第一部分。在胚轴中,线粒体是主要的能量产生者。为了更好地理解盐度对线粒体功能的影响,本研究聚焦于NaCl胁迫对线粒体蛋白质组的作用。从在250和500 mM NaCl体外培养12小时的黄羽扇豆(L. 'Mister')胚轴中分离线粒体。对从NaCl处理的胚轴中分离的线粒体蛋白质进行二维凝胶电泳,结果表明蛋白质丰度因盐度处理而发生显著变化。选择在250和500 mM NaCl处理下蛋白质表达谱均有显著变化的21个点进行串联质谱鉴定。该方法揭示了与不同代谢过程相关的蛋白质,这些蛋白质代表三羧酸循环的酶、线粒体电子传递链、参与线粒体生物发生和应激反应的酶和蛋白质。在参与线粒体生物发生的蛋白质中,发现了线粒体内膜转位酶、Tim17/22亚基、线粒体加工肽酶α-1亚基、线粒体延伸因子Tu和伴侣蛋白CPN60。最后,发现甲酸脱氢酶1在盐度下在羽扇豆胚轴线粒体中积累。结合盐度胁迫反应,包括盐度诱导的程序性细胞死亡,对鉴定出的蛋白质的功能进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a585/4372824/6f1b1442c915/11738_2013_1273_Fig1_HTML.jpg

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