Weise Andreas, Rodriguez-Franco Marta, Timm Barbara, Hermann Matthias, Link Sandra, Jost Wolfgang, Gorr Gilbert
greenovation Biotech GmbH, Bötzinger Str. 29b, 79111, Freiburg, Germany.
Appl Microbiol Biotechnol. 2006 Apr;70(3):337-45. doi: 10.1007/s00253-005-0087-6. Epub 2005 Jul 30.
We have isolated four actin (Act) genes from Physcomitrella patens and used their corresponding 5' regions for recombinant expression of the human vascular endothelial growth factor (rhVEGF121) in transiently transformed Physcomitrella protoplasts and in stable transformed lines. In the transient system, we found up to 11-fold activity of the corresponding 5' regions as compared with that of the plant constitutive 35S promoter. Moreover, the use of an optimised expression vector in which the human VEGF signal peptide was exchanged with a plant signal peptide resulted in an additional 7-fold increase in secreted rhVEGF. We found that the 5' introns of PpAct1, PpAct5 and PpAct7 are essential for high expression. The enhancing mechanisms of the introns, however, seem to be different since in the case of PpAct1, the expression level is stimulated only in the presence of the endogenous promoter, whereas the 5' introns of PpAct5 and PpAct7 stimulate expression also in combination with the 35S promoter. Beyond this, the isolated 5' regions are shown to be useful for high expression levels in transgenic moss lines with values of secreted rhVEGF up to 96 microg g(-1) dry weight.
我们从小立碗藓中分离出了四个肌动蛋白(Act)基因,并利用其相应的5'区域在瞬时转化的小立碗藓原生质体和稳定转化株系中重组表达人血管内皮生长因子(rhVEGF121)。在瞬时系统中,我们发现与植物组成型35S启动子相比,相应的5'区域活性高达11倍。此外,使用一种优化的表达载体,其中人VEGF信号肽被植物信号肽替换,导致分泌的rhVEGF增加了7倍。我们发现PpAct1、PpAct5和PpAct7的5'内含子对于高表达至关重要。然而,内含子的增强机制似乎有所不同,因为在PpAct1的情况下,表达水平仅在内源启动子存在时受到刺激,而PpAct5和PpAct7的5'内含子与35S启动子结合时也能刺激表达。除此之外,分离出的5'区域被证明可用于转基因苔藓株系中的高表达,分泌的rhVEGF值高达96μg g(-1)干重。