Graham S V, Barry J D
Wellcome Unit of Molecular Parasitology, Anderson College, University of Glasgow, Scotland.
Mol Cell Biol. 1995 Nov;15(11):5945-56. doi: 10.1128/MCB.15.11.5945.
In antigenic variation in African trypanosomes, switching of the variant surface glycoprotein (VSG) allows evasion of the mammalian host immune response. Trypanosomes first express the VSG in the tsetse fly vector, at the metacyclic stage, in preparation for transfer into the mammal. In this life cycle stage, a small, specific subset (1 to 2%) of VSGs are activated, and we have shown previously that the system of activation and expression of metacyclic VSG (M-VSG) genes is very different from that used for bloodstream VSG genes (S.V. Graham, K.R. Matthews, P.G. Shiels, and J.D. Barry, Parasitology 101:361-367, 1990). Now we show that unlike other trypanosome genes including bloodstream VSG genes, M-VSG genes are expressed from promoters subject to exclusively transcriptional regulation in a life cycle stage-dependent manner. We have located an M-VSG gene promoter, and we demonstrate that it is specifically up-regulated at the metacyclic stage. This is the first demonstration of gene expression being regulated entirely at the level of transcription among the Kinetoplastida; all other protein-coding genes examined in these organisms are, at least partly, under posttranscriptional control. The distinctive mode of expression of M-VSG genes may be due to a stochastic mechanism for metacyclic VSG activation.
在非洲锥虫的抗原变异中,变异表面糖蛋白(VSG)的转换使得寄生虫能够逃避哺乳动物宿主的免疫反应。锥虫首先在采采蝇媒介的循环后期表达VSG,为转移至哺乳动物体内做准备。在这个生命周期阶段,一小部分特定的VSG(1%至2%)被激活,我们之前已经表明,循环后期VSG(M-VSG)基因的激活和表达系统与用于血流中VSG基因的系统非常不同(S.V. Graham、K.R. Matthews、P.G. Shiels和J.D. Barry,《寄生虫学》101:361 - 367,1990)。现在我们发现,与包括血流中VSG基因在内的其他锥虫基因不同,M-VSG基因是从仅受生命周期阶段依赖性转录调控的启动子表达的。我们定位了一个M-VSG基因启动子,并证明它在循环后期阶段被特异性上调。这是动质体目基因表达完全在转录水平受到调控的首次证明;在这些生物体中检测的所有其他蛋白质编码基因至少部分受转录后控制。M-VSG基因独特的表达模式可能是由于循环后期VSG激活的随机机制。