Institute for Molecular Biotechnology, RWTH Aachen University, Worringerweg 1,Aachen, 52074, Germany.
Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6,Aachen, 52074, Germany.
Biotechnol J. 2019 Mar;14(3):e1800075. doi: 10.1002/biot.201800075. Epub 2018 May 11.
The yield of recombinant proteins in plants determines their economic competitiveness as a production platform compared to microbes and mammalian cells. The promoter, untranslated regions (UTRs) and codon usage can all contribute to the yield, but potential interactions among these components have not been examined in detail. Here the effect of two promoters (35SS and nos) and four 5'UTRs on the spatiotemporal expression of DsRed mRNA and the accumulation of DsRed protein during transient expression in tobacco (Nicotiana tabacum) mediated by Agrobacterium tumefaciens is investigated. The authors found that the mRNA levels peaked 2-3 days post-infiltration (dpi), and rapidly declined thereafter, whereas DsRed protein was first detected after ≈3 days and concentrations continued to increase until at least 5 dpi. This temporal decoupling of mRNA and protein expression was strongest in the older leaves, which also produced the lowest DsRed yields. The accumulation of DsRed linearly correlated with mRNA levels in all but the youngest leaves, where more DsRed was synthesized per mRNA molecule. This was the case for both promoters, although the nos promoter had a higher protein/mRNA ratio than the 35SS promoter. Furthermore, the type of 5'UTR affected DsRed protein accumulation by 50% starting from similar levels of mRNA. The authors concluded that DsRed mRNA levels are not the limiting factor for DsRed protein expression in plants, but that translation-associated processes such as initiation, elongation, and release are bottlenecks that should be addressed in future studies.
与微生物和哺乳动物细胞相比,植物中重组蛋白的产量决定了其作为生产平台的经济竞争力。启动子、非翻译区(UTR)和密码子使用都可以影响产量,但这些元件之间的潜在相互作用尚未得到详细研究。在这里,研究了两个启动子(35SS 和 nos)和四个 5'UTR 对 DsRed mRNA 在烟草(Nicotiana tabacum)中转瞬时表达的时空表达以及由根癌农杆菌介导的 DsRed 蛋白积累的影响。作者发现,mRNA 水平在侵染后 2-3 天(dpi)达到峰值,此后迅速下降,而 DsRed 蛋白在约 3 天后才首次检测到,并且浓度至少在 5 dpi 时继续增加。这种 mRNA 和蛋白质表达的时间解耦在较老的叶片中最强,而这些叶片产生的 DsRed 产量最低。除了最年轻的叶片外,DsRed 的积累与 mRNA 水平呈线性相关,在这些叶片中,每个 mRNA 分子合成的 DsRed 更多。这两种启动子都是如此,尽管 nos 启动子的蛋白/信使 RNA 比值高于 35SS 启动子。此外,5'UTR 的类型从相似的 mRNA 水平开始就影响了 50%的 DsRed 蛋白积累。作者得出结论,在植物中,DsRed mRNA 水平不是 DsRed 蛋白表达的限制因素,而是翻译相关过程(如起始、延伸和释放)是未来研究中应解决的瓶颈。