Pays E
Department of Molecular Biology, Free University of Brussels, Rhode St. Genèse, Belgium.
Biol Cell. 1988;64(2):121-30. doi: 10.1016/0248-4900(88)90071-8.
Among the large collection of antigen genes present in the Trypanosoma brucei genome, only one is usually transcribed at a time when the parasites develop in the mammalian bloodstream. The antigen gene is transcribed in a telomeric expression site, together with other genes whose function is unknown. The nature of the RNA polymerase and transcription promoter, as well as the overall organization of the transcription unit, suggests that transcription of the antigen gene is of the ribosomal type. This transcription rapidly stops when the temperature of the parasite medium is lowered, probably accounting for the gene inactivation in the procyclic form of the insect midgut. Antigen gene expression resumes in 2 steps: first, induction of specific metacyclic variants occurs in the fly salivary glands, then injection into the blood reactivates the expression site silenced at the procyclic stage. Several telomeres can act as alternative expression sites, but the mechanism for expression-site switching is unknown. In a given expression site, the specificity of the antigen gene can change following gene conversion, telomeric reciprocal recombination, or point mutation. The alternate use of these mechanisms leads to the successive appearance of a very high number of antigenic variants, as well as to rapid evolution of the antigen gene repertoire. The relative extent of homology between nontelomeric antigen genes and the expression site may condition the programming of antigenic variation late in chronic infection, as well as the generation of chimaeric antigen genes.
在布氏锥虫基因组中存在的大量抗原基因集合里,当寄生虫在哺乳动物血液中发育时,通常一次只有一个基因被转录。该抗原基因与其他功能未知的基因一起在端粒表达位点被转录。RNA聚合酶和转录启动子的性质,以及转录单元的整体组织,表明抗原基因的转录属于核糖体类型。当寄生虫培养基的温度降低时,这种转录会迅速停止,这可能是昆虫中肠前循环形式中基因失活的原因。抗原基因的表达分两步恢复:首先,在苍蝇唾液腺中诱导特定的循环后期变体,然后注入血液会重新激活在前循环阶段沉默的表达位点。几个端粒可以作为替代表达位点,但表达位点切换的机制尚不清楚。在给定的表达位点,抗原基因的特异性可以在基因转换、端粒相互重组或点突变后发生变化。这些机制的交替使用导致大量抗原变体的相继出现,以及抗原基因库的快速进化。非端粒抗原基因与表达位点之间的同源性相对程度可能会影响慢性感染后期抗原变异的编程,以及嵌合抗原基因的产生。