Agarwal Priyanka, Kumar Rahul, Pareek Amit, Sharma Arun K
Department of Plant Molecular Biology, University of Delhi South Campus, New Delhi, 110021, India.
Repository of Tomato Genomics Resources, Department of Plant Sciences, University of Hyderabad, Hyderabad, 500046, India.
Mol Genet Genomics. 2017 Feb;292(1):145-156. doi: 10.1007/s00438-016-1262-4. Epub 2016 Oct 27.
Isolation and functional characterization of tissue- and stage-specific gene promoters is beneficial for genetic improvement of economically important crops. Here, we have characterized a putative promoter of a ripening-induced gene RIP1 (Ripening induced protein 1) in tomato. Quantification of the transcript level of RIP1 showed that its expression is fruit preferential, with maximum accumulation in red ripe fruits. To test the promoter activity, we made a reporter construct by cloning 1450 bp putative RIP1 promoter driving the GUS (ß-glucuronidase) gene expression and generated stable transgenic lines in tomato and Arabidopsis. Histochemical and fluorometric assays validated the fruit-specific expression of RIP1 as the highest GUS activity was found in red ripe tomatoes. Similarly, we detected high levels of GUS activity in the siliques of Arabidopsis. On the contrary, weak GUS activity was found in the flower buds in both tomato and Arabidopsis. To characterize the specific regions of the RIP1 promoter that might be essential for its maximum activity and specificity in fruits, we made stable transgenic lines of tomato and Arabidopsis with 5'-deletion constructs. Characterization of these transgenic plants showed that the full length promoter is essential for its function. Overall, we report the identification and characterization of a ripening-induced promoter of tomato, which would be useful for the controlled manipulation of the ripening-related agronomic traits in genetic manipulation studies in future.
分离和鉴定组织及阶段特异性基因启动子,有助于对经济作物进行遗传改良。在此,我们对番茄中一个成熟诱导基因RIP1(成熟诱导蛋白1)的假定启动子进行了鉴定。RIP1转录水平的定量分析表明,其表达具有果实偏好性,在红色成熟果实中积累量最高。为了检测启动子活性,我们构建了一个报告基因载体,通过克隆1450 bp假定的RIP1启动子来驱动GUS(β-葡萄糖醛酸酶)基因表达,并在番茄和拟南芥中获得了稳定的转基因株系。组织化学和荧光分析验证了RIP1在果实中的特异性表达,因为在红色成熟番茄中发现了最高的GUS活性。同样,我们在拟南芥的角果中也检测到了高水平的GUS活性。相反,在番茄和拟南芥的花蕾中发现GUS活性较弱。为了鉴定RIP1启动子中对其在果实中的最大活性和特异性可能至关重要的特定区域,我们用5'-缺失构建体获得了番茄和拟南芥的稳定转基因株系。对这些转基因植物的鉴定表明,全长启动子对其功能至关重要。总体而言,我们报告了番茄中一个成熟诱导启动子的鉴定和特性,这将有助于未来在遗传操作研究中对与成熟相关的农艺性状进行可控操作。