Gubler F, Raventos D, Keys M, Watts R, Mundy J, Jacobsen J V
Co-operative Research Centre for Plant Science, Canberra City, ACT, Australia.
Plant J. 1999 Jan;17(1):1-9. doi: 10.1046/j.1365-313x.1999.00346.x.
GAMYB is an MYB transcription factor which is expressed in cereal aleurone cells in response to gibberellin (GA). HvGAMYB binds to the TAACAAA box of a high-pl alpha-amylase gene promoter and transcriptionally activates its expression. In this study, we examined the role of HvGAMYB in activating expression of other GA-regulated genes encoding hydrolytic enzymes. In transient expression experiments, HvGAMYB transactivated expression of reporter genes fused to a low-pl alpha-amylase gene promoter, an EII (1-3, 1-4)-beta-glucanase gene promoter and a cathepsin B-like protease promoter. HvGAMYB DNA binding specificity was determined using a PCR-based random site selection using HvGAMYB fusion protein isolated from E. coli. The deduced consensus closely resembled gibberellin response elements in alpha-amylase promoters. Functional analysis of HvGAMYB by transient expression of C terminal HvGAMYB deletions in barley aleurone cells identified two transcriptional activation domains (TADs) which function in transcriptional regulation of both high- and low-pl alpha-amylase promoters. The same TADs were identified using a heterologous yeast expression system. Together, these results indicate that HvGAMYB has two TADs. These domains are C-terminal to its DNA-binding domain.
GAMYB是一种MYB转录因子,在谷类糊粉层细胞中响应赤霉素(GA)而表达。HvGAMYB与高表达α-淀粉酶基因启动子的TAACAAA框结合,并转录激活其表达。在本研究中,我们研究了HvGAMYB在激活其他编码水解酶的GA调控基因表达中的作用。在瞬时表达实验中,HvGAMYB反式激活了与低表达α-淀粉酶基因启动子、EII(1-3,1-4)-β-葡聚糖酶基因启动子和组织蛋白酶B样蛋白酶启动子融合的报告基因的表达。使用从大肠杆菌中分离的HvGAMYB融合蛋白,通过基于PCR的随机位点选择来确定HvGAMYB的DNA结合特异性。推导的共有序列与α-淀粉酶启动子中的赤霉素反应元件非常相似。通过在大麦糊粉层细胞中瞬时表达C末端HvGAMYB缺失对HvGAMYB进行功能分析,确定了两个转录激活结构域(TAD),它们在高表达和低表达α-淀粉酶启动子的转录调控中起作用。使用异源酵母表达系统也鉴定出了相同的TAD。这些结果共同表明HvGAMYB有两个TAD。这些结构域位于其DNA结合结构域的C末端。