Elorza Alvaro, Roschzttardtz Hannetz, Gómez Isabel, Mouras Armand, Holuigue Loreto, Araya Alejandro, Jordana Xavier
Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, P. Universidad Católica de Chile, Casilla 114-D, Santiago.
Plant Cell Physiol. 2006 Jan;47(1):14-21. doi: 10.1093/pcp/pci218. Epub 2005 Oct 25.
Three nuclear genes, SDH2-1, SDH2-2 and SDH2-3, encode the essential iron-sulfur subunit of mitochondrial complex II in Arabidopsis thaliana. SDH2-1 and SDH2-2 probably arose via a recent duplication event and we reported that both are expressed in all organs from adult plants. In contrast, transcripts from SDH2-3 were not detected. Here we present data demonstrating that SDH2-3 is specifically expressed during seed development. SDH2-3 transcripts appear during seed maturation, persist through desiccation, are abundant in dry seeds and markedly decline during germination. Analysis of transgenic Arabidopsis plants carrying the SDH2-3 promoter fused to the beta-glucuronidase reporter gene shows that the SDH2-3 promoter is activated in the embryo during maturation, from the bent-cotyledon stage. beta-Glucuronidase expression correlates with the appearance of endogenous SDH2-3 transcripts, suggesting that control of this nuclear gene is achieved through transcriptional regulation. Furthermore, progressive deletions of this promoter identified a 159 bp region (-223 to -65) important for SDH2-3 transcriptional activation in seeds. Interestingly, the SDH2-3 promoter remains active in embryonic tissues during germination and post-germinative growth, and is turned off in vegetative tissues (true leaves). In contrast to SDH2-3 transcripts, SDH2-1 and SDH2-2 transcripts are barely detected in dry seeds and increase during germination and post-germinative growth. The opposite expression patterns of SDH2 nuclear genes strongly suggest that during germination the embryo-specific SDH2-3 is replaced by SDH2-1 or SDH2-2 in mitochondrial complex II.
三个核基因,SDH2-1、SDH2-2和SDH2-3,编码拟南芥线粒体复合物II的必需铁硫亚基。SDH2-1和SDH2-2可能是通过最近的一次复制事件产生的,我们报道这两个基因在成年植物的所有器官中均有表达。相比之下,未检测到SDH2-3的转录本。在此,我们提供的数据表明SDH2-3在种子发育过程中特异性表达。SDH2-3转录本在种子成熟期间出现,在干燥过程中持续存在,在干种子中含量丰富,并在萌发过程中显著下降。对携带与β-葡萄糖醛酸酶报告基因融合的SDH2-3启动子的转基因拟南芥植物进行分析表明,从弯子叶期开始,SDH2-3启动子在胚胎成熟过程中被激活。β-葡萄糖醛酸酶的表达与内源性SDH2-3转录本的出现相关,表明该核基因的调控是通过转录调控实现的。此外,对该启动子进行逐步缺失分析,确定了一个对种子中SDH2-3转录激活重要的159 bp区域(-223至-65)。有趣的是,SDH2-3启动子在萌发和萌发后生长期间在胚胎组织中保持活性,并在营养组织(真叶)中关闭。与SDH2-3转录本相反,SDH2-1和SDH2-2转录本在干种子中几乎检测不到,并在萌发和萌发后生长期间增加。SDH2核基因相反的表达模式强烈表明,在萌发过程中,线粒体复合物II中胚胎特异性的SDH2-3被SDH2-1或SDH2-2所取代。