Marzábal Pau, Gas Elisabet, Fontanet Pilar, Vicente-Carbajosa Jesús, Torrent Margarita, Ludevid M Dolores
Consorci CSIC-IRTA, Jordi Girona 18-26, 08034 Barcelona, Spain.
Plant Mol Biol. 2008 Jul;67(5):441-54. doi: 10.1007/s11103-008-9325-5. Epub 2008 Apr 1.
Maize PBF (prolamin-box binding factor) belongs to the Dof class of plant specific transcription factors containing one highly conserved zinc finger DNA-binding domain, called Dof (DNA binding with one finger) domain. Maize PBF trans-activates the gamma-zein gene (gammaZ) promoter in developing maize seeds as shown by transient expression in maize endosperms. Co-transfection of a gammaZ:GUS construct with 35S:PBF resulted in a sevenfold increase in GUS expression, however, PBF mutation in Cys residues within the Dof domain abolishes both, binding to DNA and the capacity to activate gammaZ promoter. We present two pieces of evidence that PBF transactivates gammaZ promoter by binding to the Pb3 motif (TGTAAAG). First, recombinant Dof domain of PBF (bdPBF) specifically recognized Pb3 site as shown by gel mobility shift assays and second, co-expression of PBF with gammaZ promoter mutated in Pb3 motif suppressed PBF trans-activation capacity. Immunocytochemical analysis on developing endosperm sections shows that PBF is localized in the nuclei of the peripheral layer cells of starchy endosperm, the tissue in which the initial accumulation of gamma-zein protein occurs. By contrast, PBF is detected in the cytosol of the starchy endosperm cells newly differentiated from aleurone daughter cells, where gamma-zein was absent. Taken together these data indicate that maize PBF plays an essential role in the regulation of the temporal and spatial expression of gammaZ gene.
玉米PBF(醇溶蛋白盒结合因子)属于植物特异性转录因子的Dof类,含有一个高度保守的锌指DNA结合结构域,称为Dof(单指DNA结合)结构域。如在玉米胚乳中的瞬时表达所示,玉米PBF在发育中的玉米种子中反式激活γ-玉米醇溶蛋白基因(γZ)启动子。将γZ:GUS构建体与35S:PBF共转染导致GUS表达增加了7倍,然而,Dof结构域内半胱氨酸残基的PBF突变消除了与DNA的结合以及激活γZ启动子的能力。我们提供了两条证据表明PBF通过与Pb3基序(TGTAAAG)结合来反式激活γZ启动子。第一,如凝胶迁移率变动分析所示,PBF的重组Dof结构域(bdPBF)特异性识别Pb3位点;第二,PBF与在Pb3基序中发生突变的γZ启动子共表达抑制了PBF的反式激活能力。对发育中的胚乳切片进行免疫细胞化学分析表明,PBF定位于淀粉质胚乳外周层细胞的细胞核中,γ-玉米醇溶蛋白最初在此组织中积累。相比之下,在从糊粉层子细胞新分化出的淀粉质胚乳细胞的细胞质中检测到PBF,而这些细胞中不存在γ-玉米醇溶蛋白。综合这些数据表明,玉米PBF在γZ基因的时空表达调控中起重要作用。