Maugenest S, Martinez I, Godin B, Perez P, Lescure A M
Laboratoire de Biologie des Semences, INRA INA-PG, Versailles, France.
Plant Mol Biol. 1999 Feb;39(3):503-14. doi: 10.1023/a:1006131506193.
Up to 80% of Zea mays L. grain phosphorus is stored in the form of phytin in the embryo. Our objective is to determine the control of phytin mobilization during germination and seedling growth. A maize phytase cDNA, phy S11, has been previously characterized (Maugenest et al., Biochem J 322: 511-517, 1997). In the present work, phy S11 was used to screen a maize genomic library and two distinct genes, PHYT I and PHYT II, were isolated and sequenced. The transcribed sequences of these two genes presented a strong homology whereas the untranscribed upstream and downstream sequences appeared very different. Northern blot analysis and in situ hybridization showed a high accumulation of phytase mRNA at the early steps of germination in the coleorhiza, radicle cortex and coleoptile parenchyma. Phytase expression was also detected at a lower extent in the scutellum. In adult plants, northern blot analyses revealed low but significant levels of phytase mRNA in the roots. In situ hybridizations on root cross-sections localized phytase mRNA in rhizodermis, endodermis and pericycle layers. Immunolocalization analysis showed phytase accumulation at the same sites as its mRNA. A RT-PCR approach was used in an attempt to discriminate between the transcripts from each gene in the different situations. These experiments indicate that both genes are expressed during germination, whereas only PHYT I is expressed in adult roots. This suggests that signals responsible for phytase gene expression in roots are different from those responsible for gene expression during germination.
高达80%的玉米籽粒磷以肌醇六磷酸钙镁的形式储存在胚中。我们的目标是确定发芽和幼苗生长过程中肌醇六磷酸钙镁动员的调控机制。一种玉米植酸酶cDNA,phy S11,先前已被鉴定(Maugenest等人,《生物化学杂志》322:511 - 517,1997)。在本研究中,利用phy S11筛选玉米基因组文库,分离并测序了两个不同的基因,PHYT I和PHYT II。这两个基因的转录序列具有高度同源性,而未转录的上游和下游序列则差异很大。Northern杂交分析和原位杂交显示,在发芽早期,胚根鞘、胚根皮层和胚芽鞘薄壁组织中植酸酶mRNA大量积累。在盾片中也检测到较低水平的植酸酶表达。在成年植株中,Northern杂交分析显示根中植酸酶mRNA水平较低但显著。对根横切面的原位杂交将植酸酶mRNA定位在根表皮、内皮层和中柱鞘层。免疫定位分析表明植酸酶在与其mRNA相同的位点积累。采用RT-PCR方法试图区分不同情况下每个基因的转录本。这些实验表明,两个基因在发芽过程中均表达,而仅PHYT I在成年根中表达。这表明负责根中植酸酶基因表达的信号与负责发芽过程中基因表达的信号不同。