Pimentel Catarina, Van Der Straeten Dominique, Pires Euclides, Faro Carlos, Rodrigues-Pousada Claudina
Departamento de Biologia Molecular e Biotecnologia do Centro de Neurociências de Coimbra, Universidade de Coimbra, Coimbra, Portugal.
FEBS J. 2007 May;274(10):2523-39. doi: 10.1111/j.1742-4658.2007.05787.x. Epub 2007 Apr 13.
Cardosin A and cardosin B are two aspartic proteases mainly found in the pistils of cardoon Cynara cardunculus L., whose flowers are traditionally used in several Mediterranean countries in the manufacture of ewe's cheese. We have been characterizing cardosins at the biochemical, structural and molecular levels. In this study, we show that the cardoon aspartic proteases are encoded by a multigene family. The genes for cardosin A and cardosin B, as well as those for two new cardoon aspartic proteases, designated cardosin C and cardosin D, were characterized, and their expression in C. cardunculus L. was analyzed by RT-PCR. Together with cardosins, a partial clone of the cyprosin B gene was isolated, revealing that cardosin and cyprosin genes coexist in the genome of the same plant. As a first approach to understanding what dictates the flower-specific pattern of cardosin genes, the respective gene 5' regulatory sequences were fused with the reporter beta-glucuronidase and introduced into Arabidopsis thaliana. A subsequent deletion analysis of the promoter region of the cardosin A gene allowed the identification of a region of approximately 500 bp essential for gene expression in transgenic flowers. Additionally, the relevance of the leader intron of the cardosin A and B genes for gene expression was evaluated. Our data showed that the leader intron is essential for cardosin B gene expression in A. thaliana. In silico analysis revealed the presence of potential regulatory motifs that lay within the aforementioned regions and therefore might be important in the regulation of cardosin expression.
卡多辛A和卡多辛B是两种天冬氨酸蛋白酶,主要存在于刺菜蓟(Cynara cardunculus L.)的雌蕊中,其花朵在几个地中海国家传统上用于制作母羊奶酪。我们一直在从生化、结构和分子水平对卡多辛进行表征。在本研究中,我们表明刺菜蓟天冬氨酸蛋白酶由一个多基因家族编码。对卡多辛A和卡多辛B的基因,以及另外两种新的刺菜蓟天冬氨酸蛋白酶(命名为卡多辛C和卡多辛D)的基因进行了表征,并通过逆转录聚合酶链反应(RT-PCR)分析了它们在刺菜蓟中的表达。与卡多辛一起,分离出了环孢菌素B基因的一个部分克隆,揭示了卡多辛和环孢菌素基因共存于同一植物的基因组中。作为理解决定卡多辛基因花特异性模式因素的第一步,将各自基因的5'调控序列与报告基因β-葡萄糖醛酸酶融合,并导入拟南芥。随后对卡多辛A基因启动子区域的缺失分析,使得能够鉴定出转基因花中基因表达所必需的大约500 bp的区域。此外,还评估了卡多辛A和B基因的前导内含子对基因表达的相关性。我们的数据表明,前导内含子对拟南芥中卡多辛B基因的表达至关重要。电子分析揭示了上述区域内存在潜在的调控基序,因此可能在卡多辛表达的调控中起重要作用。