Joubès J, Phan T H, Just D, Rothan C, Bergounioux C, Raymond P, Chevalier C
Unité de Physiologie Végétale, Institut de Biologie Végétale Moléculaire, Centre de Recherche Institut National de la Recherche Agronomique-Bordeaux, BP 81, 33883 Villenave d'Ornon cedex, France.
Plant Physiol. 1999 Nov;121(3):857-69. doi: 10.1104/pp.121.3.857.
Following fruit set, the early development of tomato (Lycopersicon esculentum Mill.) fruit comprises two distinct phases: a cell division phase and a consecutive phase of cell expansion until the onset of ripening. In this study, we analyzed cytological and molecular changes characterizing these early phases of tomato fruit development. First we investigated the spatial and temporal regulation of the mitotic activity during fruit development. The DNA content of isolated nuclei from the different fruit tissues was determined by flow cytometry analysis. The results confirm the data of mitotic activity measurements and show that cell differentiation, leading to expanded cells, is characterized by endoreduplication. Second, we isolated two cDNAs, named Lyces;CDKA1 (accession no. Y17225) and Lyces;CDKA2 (accession no. Y17226), encoding tomato homologs of the cyclin-dependent kinase (CDK) p34(cdc2). Tomato CDKA gene expression was followed at both the transcriptional and translational levels during fruit development. The transcripts for Lyces;CDKA1 and Lyces;CDKA2 and the corresponding CDKA proteins are predominantly accumulated during the phase of cell division between anthesis and 5 d post anthesis (DPA). In whole fruits, the maximum CDK activity was obtained between 5 and 10 DPA. The determination of the kinase activity using protein extracts from the different fruit tissues was in agreement with mitotic activity analysis. It showed the particular disappearance of the activity in the gel tissue as early as 15 DPA. The overall data of CDK activity measurements suggest a strong post-translational regulation of CDK at the temporal and spatial levels during early tomato fruit development.
坐果后,番茄(Lycopersicon esculentum Mill.)果实的早期发育包括两个不同阶段:细胞分裂阶段和随后的细胞扩展阶段,直至成熟开始。在本研究中,我们分析了表征番茄果实发育早期阶段的细胞学和分子变化。首先,我们研究了果实发育过程中有丝分裂活性的时空调控。通过流式细胞术分析确定了从不同果实组织分离的细胞核的DNA含量。结果证实了有丝分裂活性测量的数据,并表明导致细胞扩展的细胞分化以内复制为特征。其次,我们分离了两个cDNA,命名为Lyces;CDKA1(登录号Y17225)和Lyces;CDKA2(登录号Y17226),它们编码细胞周期蛋白依赖性激酶(CDK)p34(cdc2)的番茄同源物。在果实发育过程中,对番茄CDKA基因表达进行了转录和翻译水平的跟踪。Lyces;CDKA1和Lyces;CDKA2的转录本以及相应的CDKA蛋白主要在开花期至花后5天(DPA)的细胞分裂阶段积累。在整个果实中,最大的CDK活性在花后5至10天获得。使用来自不同果实组织的蛋白质提取物测定激酶活性与有丝分裂活性分析结果一致。结果表明,早在花后15天,凝胶组织中的活性就特别消失了。CDK活性测量的总体数据表明,在番茄果实发育早期,CDK在时间和空间水平上受到强烈的翻译后调控。