Su Li-Hsin, Lee Gilbert A, Huang Yu-Chang, Chen Yi-Hsiu, Sun Chin-Hung
Department of Parasitology, College of Medicine, National Taiwan University, Taipei 100, Taiwan, ROC.
Mol Biochem Parasitol. 2007 Dec;156(2):124-35. doi: 10.1016/j.molbiopara.2007.07.015. Epub 2007 Jul 31.
Two systems for stable transfection of Giardia have been established using selection either by neomycin or by puromycin. We asked if these selection systems themselves influenced expression of endogenous giardial genes. Northern blot analysis showed a approximately 1.4 to approximately 7-fold increase in the encystation-induced cyst wall protein 1 (cwp1), cwp2, and gmyb2 gene transcripts in the drug selected cell lines during vegetative growth, compared with untransfected cells. However, the levels of the constitutive ran, lrp3, or alpha2-tubulin gene transcripts decreased slightly or did not change in these stably transfected cell lines. Part of the effect could be due to drug selection, since treatment of untransfected cells with G418 or puromycin also had similar effects. Nuclear run-on assays showed that part of the effect comes from an increase in transcription initiation rate. The levels of CWP and cyst formation during vegetative growth also increased in the transfected cell lines. Using proteomic technologies, we identified eight genes whose expression is upregulated in neomycin selected cell lines, including phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase, ornithine carbamoyltransferase, carbamate kinase, orf 16424, cyclophilin, co-chaperone-like p21, and bip. Six of these are also upregulated in puromycin selected cell lines. Our results indicate that transfection and drug selection, per se, can alter expression of genes involved in metabolism, protein folding, and differentiation status in Giardia.
利用新霉素或嘌呤霉素进行筛选,已建立了两种用于贾第虫稳定转染的系统。我们探究了这些筛选系统本身是否会影响贾第虫内源基因的表达。Northern印迹分析表明,与未转染的细胞相比,在营养生长期间,药物筛选的细胞系中,包囊化诱导的囊壁蛋白1(cwp1)、cwp2和gmyb2基因转录本增加了约1.4至约7倍。然而,在这些稳定转染细胞系中,组成型的ran、lrp3或α2-微管蛋白基因转录本水平略有下降或没有变化。部分影响可能归因于药物筛选,因为用G418或嘌呤霉素处理未转染的细胞也有类似的效果。核运行分析表明,部分影响来自转录起始速率的增加。在转染的细胞系中,营养生长期间CWP的水平和包囊形成也增加了。利用蛋白质组学技术,我们鉴定出八个在新霉素筛选的细胞系中表达上调的基因,包括磷酸甘油酸激酶、甘油醛-3-磷酸脱氢酶、鸟氨酸氨甲酰基转移酶、氨基甲酸激酶、orf 16424、亲环蛋白、共伴侣样p21和Bip。其中六个在嘌呤霉素筛选的细胞系中也上调。我们的结果表明,转染和药物筛选本身可以改变贾第虫中参与代谢、蛋白质折叠和分化状态的基因的表达。