Baud Sébastien, Dichow Neel Reinhard, Kelemen Zsolt, d'Andréa Sabine, To Alexandra, Berger Nathalie, Canonge Michel, Kronenberger Jocelyne, Viterbo David, Dubreucq Bertrand, Lepiniec Loïc, Chardot Thierry, Miquel Martine
Institut Jean-Pierre Bourgin, UMR Biologie des semences, INRA/AgroParisTech, F-78000 Versailles, France.
Plant Cell Physiol. 2009 Aug;50(8):1463-78. doi: 10.1093/pcp/pcp092. Epub 2009 Jun 20.
The hydroxysteroid dehydrogenase HSD1, identified in the proteome of oil bodies from mature Arabidopsis seeds, is encoded by At5g50600 and At5g50700, two gene copies anchored on a duplicated region of chromosome 5. Using a real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) approach, the accumulation of HSD1 mRNA was shown to be specifically and highly induced in oil-accumulating tissues of maturing seeds. HSD1 mRNA disappeared during germination. The activity of HSD1 promoter and the localization of HSD1 transcripts by in situ hybridization were consistent with this pattern. A complementary set of molecular and genetic analyses showed that HSD1 is a target of LEAFY COTYLEDON2, a transcriptional regulator able to bind the promoter of HSD1. Immunoblot analyses and immunolocalization experiments using anti-AtHSD1 antibodies established that the pattern of HSD1 deposition faithfully reflected mRNA accumulation. At the subcellular level, the study of HSD1:GFP fusion proteins showed the targeting of HSD1 to the surface of oil bodies. Transgenic lines overexpressing HSD1 were then obtained to test the importance of proper transcriptional regulation of HSD1 in seeds. Whereas no impact on oil accumulation could be detected, transgenic seeds exhibited lower cold and light requirements to break dormancy, germinate and mobilize storage lipids. Interestingly, overexpressors of HSD1 over-accumulated HSD1 protein in seeds but not in vegetative organs, suggesting that post-transcriptional regulations exist that prevent HSD1 accumulation in tissues deprived of oil bodies.
在成熟拟南芥种子油体蛋白质组中鉴定出的羟基类固醇脱氢酶HSD1,由At5g50600和At5g50700编码,这两个基因拷贝锚定在5号染色体的一个重复区域上。使用实时定量逆转录聚合酶链反应(RT-PCR)方法,结果表明HSD1 mRNA的积累在成熟种子的油积累组织中受到特异性和高度诱导。HSD1 mRNA在种子萌发过程中消失。HSD1启动子的活性以及原位杂交对HSD1转录本的定位与这种模式一致。一系列互补的分子和遗传分析表明,HSD1是LEAFY COTYLEDON2的靶标,LEAFY COTYLEDON2是一种能够结合HSD1启动子的转录调节因子。使用抗AtHSD1抗体进行的免疫印迹分析和免疫定位实验表明,HSD1沉积模式忠实地反映了mRNA的积累。在亚细胞水平上,对HSD1:GFP融合蛋白的研究表明HSD1定位于油体表面。随后获得了过表达HSD1的转基因株系,以测试种子中HSD1适当转录调控的重要性。虽然未检测到对油积累的影响,但转基因种子在打破休眠、萌发和动员储存脂质方面表现出对低温和光照的需求较低。有趣的是,HSD1过表达体在种子中过度积累HSD1蛋白,但在营养器官中没有,这表明存在转录后调控机制,可防止HSD1在缺乏油体的组织中积累。