Vicente-Carbajosa J, Oñate L, Lara P, Diaz I, Carbonero P
Departamento Biotecnología-UPM, Madrid, Spain.
Plant J. 1998 Mar;13(5):629-40. doi: 10.1111/j.1365-313x.1998.00068.x.
A cDNA encoding a bZIP transcription factor was obtained from barley endosperm and used to identify the corresponding gene from a genomic library. The gene, designated Blz1, contained six exons and five introns, plus a 442 nt-long 5'-untranslated leader sequence, and was located on chromosome 5H. The Blz1 mRNA was detected early in endosperm development and was also expressed in roots and leaves. The BLZ1 protein was a potent transcriptional activator in a yeast system; 85% of its activity was associated with the first 203 amino acid residues at the N-terminus, which included two acidic regions. Presumptive involvement of Blz1 in the regulation of gene expression in endosperm was ascertained by the DNA-binding properties of BLZ1 in electrophoretic mobility shift assays (EMSA) and by transient expression in barley developing endosperms, using, as effectors, Blz1 in both sense and anti-sense orientations. In the co-bombardment experiments, the beta-glucuronidase (GUS) reported gene responded to Blz1 if under the control of the endosperm-specific ltr1 promoter or under a synthetic promoter containing the endosperm box of gene Hor2. Sucrose synthase promoters Ss1 and Ss2 and synthetic promoters containing mutated sequences of Hor2 were unaffected in trans by Blz1.
从大麦胚乳中获得了一个编码bZIP转录因子的cDNA,并用于从基因组文库中鉴定相应基因。该基因命名为Blz1,包含6个外显子和5个内含子,外加一个442 nt长的5'非翻译前导序列,位于5H染色体上。Blz1 mRNA在胚乳发育早期被检测到,在根和叶中也有表达。BLZ1蛋白在酵母系统中是一种有效的转录激活因子;其85%的活性与N端的前203个氨基酸残基相关,其中包括两个酸性区域。通过电泳迁移率变动分析(EMSA)中BLZ1的DNA结合特性以及在大麦发育胚乳中的瞬时表达,使用正义和反义方向的Blz1作为效应物,确定了Blz1可能参与胚乳中基因表达的调控。在共轰击实验中,如果β-葡萄糖醛酸酶(GUS)报告基因受胚乳特异性ltr1启动子控制或受含有基因Hor2胚乳盒的合成启动子控制,则对Blz1有反应。蔗糖合酶启动子Ss1和Ss2以及含有Hor2突变序列的合成启动子在反式中不受Blz1影响。