Pays E, Vanhamme L, Berberof M
Department of Molecular Biology, Univeristy of Brussels, Rhode Saint Genèse, Belgium.
Annu Rev Microbiol. 1994;48:25-52. doi: 10.1146/annurev.mi.48.100194.000325.
The major surface antigens of African trypanosomes, variant surface glycoprotein (VSG) and procyclin, are typical markers of their respective developmental stages, the bloodstream form and the insect-specific procyclic form. Although the role of procyclin is still unclear, variation of the VSG in the blood allows the parasite to escape the immune response of the host and develop a chronic infection. In this review, we discuss the available information concerning the genetic mechanisms that control the expression of VSG and procyclin during the life-cycle of the trypanosome. Unlike other eukaryotes, trypanosomes do not appear to primarily control the expression of their genes through a specific modulation of promoter activity. Antigenic variation in the bloodstream results either from DNA rearrangements or from a change in telomeric chromatin structure, and stage-specific regulation of antigen synthesis is linked to differential control of RNA elongation, processing, stability, and/or translation. Trypanosomes' apparent lack of transcription-initiation control probably relates to the general organization of genes in long polycistronic transcription units. Only two promoters for protein-encoding genes, those of VSG and procyclin, are known in trypanosomes, and these share properties with the ribosomal gene promoter.
非洲锥虫的主要表面抗原,即变异表面糖蛋白(VSG)和前环素,是其各自发育阶段的典型标志物,分别为血液内期形式和昆虫特异性前循环期形式。尽管前环素的作用仍不清楚,但血液中VSG的变异使寄生虫能够逃避宿主的免疫反应并发展为慢性感染。在这篇综述中,我们讨论了有关在锥虫生命周期中控制VSG和前环素表达的遗传机制的现有信息。与其他真核生物不同,锥虫似乎并非主要通过启动子活性的特定调节来控制其基因的表达。血液中的抗原变异要么源于DNA重排,要么源于端粒染色质结构的变化,并且抗原合成的阶段特异性调节与RNA延伸、加工、稳定性和/或翻译的差异控制相关。锥虫明显缺乏转录起始控制可能与长多顺反子转录单元中基因的总体组织有关。在锥虫中,仅知道两个用于蛋白质编码基因的启动子,即VSG和前环素的启动子,并且这些启动子与核糖体基因启动子具有共同特性。