González-Calle Virginia, Iglesias-Fernández Raquel, Carbonero Pilar, Barrero-Sicilia Cristina
Centro de Biotecnología y Genómica de Plantas (UPM-INIA). ETSI Agrónomos, Universidad Politécnica de Madrid, Campus de Montegancedo, Pozuelo de Alarcón, 28223, Madrid, Spain,
Planta. 2014 Sep;240(3):539-52. doi: 10.1007/s00425-014-2105-3. Epub 2014 Jun 24.
BdDOF24 interacting with BdGAMYB regulates the BdCathB gene upon germination. During barley seed germination, hydrolytic enzymes (α-amylases, proteases, etc.) synthesized in the aleurone layer in response to gibberellins (GA), catalyse the mobilization of storage reserves accumulated in the endosperm during seed maturation. In Brachypodium distachyon, the BdCathB gene that encodes a Cathepsin B-like thiol-protease, orthologous to the wheat Al21 and barley HvCathB, is highly induced in germinating seeds and its expression is regulated by transcription factors (TFs) encoded by genes BdGamyb and BdDof24, orthologous to the barley HvGamyb and BPBF-HvDof24, respectively. Transcripts of both TF genes increase during germination and treatments with abscisic acid (ABA) or paclobutrazol (PAC, an inhibitor of GA biosynthesis) decrease mRNA expression of BdGamyb but do not affect that of BdDof24. Besides, proteins BdDOF24 and BdGAMYB interact in yeast-2 hybrid systems and in plant nuclei, and in transient expression assays in aleurone layers BdDOF24 is a transcriptional repressor and BdGAMYB is an activator of the BdCathB promoter, as occurs with the putative orthologous in barley BPBF-HvDOF24 and HvGAMYB. However, when both TFs are co-bombarded, BdDOF24 enhances the activation driven by BdGAMYB while BPBF-HvDOF24 strongly decreases the HvGAMYB-mediated activation of the BdCathB promoter. The different results obtained when BdDOF24 and BPBF-HvDOF24 interact with BdGAMYB and HvGAMYB are discussed.
与BdGAMYB相互作用的BdDOF24在种子萌发时调控BdCathB基因。在大麦种子萌发过程中,糊粉层响应赤霉素(GA)合成的水解酶(α-淀粉酶、蛋白酶等)催化种子成熟期间胚乳中积累的贮藏物质的动员。在二穗短柄草中,编码组织蛋白酶B样硫醇蛋白酶的BdCathB基因与小麦Al21和大麦HvCathB直系同源,在萌发种子中被高度诱导,其表达受分别与大麦HvGamyb和BPBF-HvDof24直系同源的基因BdGamyb和BdDof24编码的转录因子(TFs)调控。两个TF基因的转录本在萌发期间增加,用脱落酸(ABA)或多效唑(PAC,GA生物合成抑制剂)处理会降低BdGamyb的mRNA表达,但不影响BdDof24的表达。此外,蛋白质BdDOF24和BdGAMYB在酵母双杂交系统和植物细胞核中相互作用,在糊粉层的瞬时表达试验中,BdDOF24是转录抑制因子,BdGAMYB是BdCathB启动子的激活因子,大麦中的假定直系同源物BPBF-HvDOF24和HvGAMYB也是如此。然而,当两种TFs共轰击时,BdDOF24增强了BdGAMYB驱动的激活,而BPBF-HvDOF24强烈降低了HvGAMYB介导的BdCathB启动子的激活。文中讨论了BdDOF24和BPBF-HvDOF24分别与BdGAMYB和HvGAMYB相互作用时获得的不同结果。