Mena Montaña, Cejudo Francisco Javier, Isabel-Lamoneda Ines, Carbonero Pilar
Laboratorio de Bioquimica y Biologia Molecular, Departmento de Biotecnologia-Universidad Politécnica de Madrid, Spain.
Plant Physiol. 2002 Sep;130(1):111-9. doi: 10.1104/pp.005561.
Functional analyses of a number of hydrolase gene promoters, induced by gibberellin (GA) in aleurone cells following germination, have identified a GA-responsive complex as a tripartite element containing a pyrimidine box motif 5'-CCTTTT-3'. We describe here that BPBF, a barley (Hordeum vulgare) transcription factor of the DOF (DNA-Binding with One Finger) class, previously shown to be an activator of reserve protein encoding genes during development, also has a role in the control of hydrolase genes following seed germination. Northern-blot, reverse transcriptase-polymerase chain reaction, and in situ hybridization analyses evidenced that the transcripts of the BPBF-encoding gene (Pbf), besides being present during endosperm development, are also expressed in aleurone cells of germinated seeds where they are induced by GA, an effect counteracted by abscisic acid. Electrophoretic mobility shift assays have shown that the BPBF protein binds specifically to the pyrimidine box motif in vitro within the different sequence contexts that naturally occur in the promoters of genes encoding a cathepsin B-like protease (Al21) and a low-isoelectric point alpha-amylase (Amy2/32b), both induced in the aleurone layers in response to GA. In transient expression experiments, BPBF repressed transcription of the Al21 promoter in GA-treated barley aleurone layers and reverted the GAMYB-mediated activation of this protease promoter.
对一些水解酶基因启动子的功能分析表明,种子萌发后糊粉层细胞中由赤霉素(GA)诱导的启动子含有一个GA反应复合体,该复合体是一个包含嘧啶框基序5'-CCTTTT-3'的三联体元件。我们在此描述,BPBF是大麦(Hordeum vulgare)DOF(单指DNA结合)类转录因子,先前已证明其在发育过程中是贮藏蛋白编码基因的激活剂,在种子萌发后水解酶基因的调控中也发挥作用。Northern杂交、逆转录聚合酶链反应和原位杂交分析表明,编码BPBF的基因(Pbf)的转录本除了在胚乳发育过程中存在外,在萌发种子的糊粉层细胞中也有表达,在那里它们由GA诱导,脱落酸可抵消这种诱导作用。电泳迁移率变动分析表明,BPBF蛋白在体外能特异性结合编码组织蛋白酶B样蛋白酶(Al21)和低等电点α-淀粉酶(Amy2/32b)的基因启动子中自然存在的不同序列背景下的嘧啶框基序,这两种基因在糊粉层中均对GA有诱导反应。在瞬时表达实验中,BPBF抑制了GA处理的大麦糊粉层中Al21启动子的转录,并逆转了GAMYB介导的该蛋白酶启动子的激活。