Qi Xiaoting, Zhang Yuxiu, Chai Tuanyao
Department of Biology, Graduate University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.
Plant Physiol. 2007 Jan;143(1):50-9. doi: 10.1104/pp.106.080283. Epub 2006 Jul 21.
The bean (Phaseolus vulgaris) stress-related gene number 2 (PvSR2) gene responds to heavy metals but not to other forms of environmental stresses. To elucidate its heavy metal-regulatory mechanism at the transcriptional level, we isolated and characterized the promoter region (-1623/+48) of PvSR2. Deletions from the 5' end revealed that a sequence between -222 and -147 relative to the transcriptional start site was sufficient for heavy metal-specific induction of the promoter region of PvSR2. Detailed analysis of this 76-bp fragment indicated that heavy metal-responsive elements were localized in two regions (-222/-188 and -187/-147), each of which could separately confer heavy metal-responsive expression on the beta-glucuronidase gene in the context of a minimal cauliflower mosaic virus 35S promoter. Region I (-222/-188) contains a motif (metal-regulatory element-like sequence) similar to the consensus metal-regulatory element of the animal metallothionein gene, and mutation of this motif eliminated the heavy metal-inducible function of region I. Region II (-187/-147) had no similarity to previously identified cis-acting elements involved in heavy metal induction, suggesting the presence of a novel heavy metal-responsive element. Transformed tobacco (Nicotiana tabacum) seedlings expressing beta-glucuronidase under control of the PvSR2 promoter region (-687/+48) showed heavy metal-specific responsive activity that depended on the type and concentration of the heavy metal and the type of organ. These findings further our understanding of the regulation of PvSR2 expression and provide a new heavy-metal-inducible promoter system in transgenic plants.
菜豆(Phaseolus vulgaris)胁迫相关基因2(PvSR2)基因对重金属有反应,但对其他形式的环境胁迫无反应。为了阐明其在转录水平上的重金属调控机制,我们分离并鉴定了PvSR2的启动子区域(-1623/+48)。从5'端进行缺失分析表明,相对于转录起始位点,-222至-147之间的序列足以实现PvSR2启动子区域的重金属特异性诱导。对这个76 bp片段的详细分析表明,重金属反应元件位于两个区域(-222/-188和-187/-147),在最小花椰菜花叶病毒35S启动子的背景下,每个区域都可以分别赋予β-葡萄糖醛酸酶基因重金属反应性表达。区域I(-222/-188)包含一个与动物金属硫蛋白基因的共有金属调控元件相似的基序(金属调控元件样序列),该基序的突变消除了区域I的重金属诱导功能。区域II(-187/-147)与先前鉴定的参与重金属诱导的顺式作用元件没有相似性,表明存在一种新型的重金属反应元件。在PvSR2启动子区域(-687/+48)控制下表达β-葡萄糖醛酸酶的转基因烟草(Nicotiana tabacum)幼苗表现出重金属特异性反应活性,该活性取决于重金属的类型和浓度以及器官类型。这些发现加深了我们对PvSR2表达调控的理解,并为转基因植物提供了一种新的重金属诱导型启动子系统。