Van der Werf A, Van Assel S, Aerts D, Steinert M, Pays E
Department of Molecular Biology, University of Brussels, Rhode St Genèse, Belgium.
EMBO J. 1990 Apr;9(4):1035-40. doi: 10.1002/j.1460-2075.1990.tb08207.x.
The AnTat 1.1 antigen type typically occurs late in a chronic infection by the EATRO 1125 stock of Trypanosoma brucei. The AnTat 1.1 gene, which is located 24 kb from a chromosome end, seems exclusively expressed by acting as a donor in gene conversion events targeted to the telomeric expression site. We report that this gene is sufficiently provided with the homology blocks required for recombination with the expression site, and is not interrupted by stop codons up to the 3' block of homology. A possible reason for its low probability of activation is an inverse orientation with respect to the proximal chromosome end, since, if correctly positioned, it is readily expressed at an early stage of infection, following gene conversion. This suggests that interactions between chromosome ends may precede and favour the rearrangements leading to antigenic variation.
AnTat 1.1抗原类型通常在布氏锥虫EATRO 1125株慢性感染后期出现。AnTat 1.1基因位于距染色体末端24 kb处,似乎仅通过在靶向端粒表达位点的基因转换事件中作为供体来表达。我们报告该基因具有与表达位点重组所需的足够同源性模块,并且在3'同源性模块之前没有被终止密码子中断。其激活概率低的一个可能原因是相对于近端染色体末端的反向取向,因为如果位置正确,它在基因转换后的感染早期很容易表达。这表明染色体末端之间的相互作用可能先于并有利于导致抗原变异的重排。