Nagoshi Y L, Alarcon C M, Donelson J E
Genetics Ph.D. Program, University of Iowa, Iowa City 52242, USA.
Mol Biochem Parasitol. 1995 Jun;72(1-2):33-45. doi: 10.1016/0166-6851(95)00062-6.
During their metacyclic developmental stage, African trypanosomes are coated with one of 12-15 variant surface glycoproteins (VSGs) that define different metacyclic variant antigen types (MVATs). The MVAT VSG genes are located near telomeres of large chromosomes and are expressed without rearrangement in the metacyclic stage. We have cloned and examined the telomere-linked MVAT5 VSG gene and its upstream expression site associated gene (ESAG I) which are separated by 4.5 kb. Within this 4.5-kb intergenic region is an 87-bp sequence that serves as a strong promoter for a luciferase reporter gene in transient transfection assays. This 87-bp sequence is similar, but not identical, to the promoter for another MVAT VSG gene. UV irradiation experiments were used to detect RNA synthesis from this MVAT5 promoter in bloodstream trypanosomes expressing an unrelated VSG. We propose that this sequence is a specific promoter for the MVAT5 VSG mRNA that occurs in about 10% of the trypanosome population during the metacyclic stage of the parasites' life cycle.
在其循环后期发育阶段,非洲锥虫表面覆盖着12至15种可变表面糖蛋白(VSG)之一,这些糖蛋白定义了不同的循环后期可变抗原类型(MVAT)。MVAT VSG基因位于大染色体的端粒附近,在循环后期阶段不经过重排即可表达。我们克隆并检测了与端粒相连的MVAT5 VSG基因及其上游表达位点相关基因(ESAG I),它们之间相隔4.5 kb。在这个4.5 kb的基因间隔区内,有一个87 bp的序列,在瞬时转染实验中,它可作为荧光素酶报告基因的强启动子。这个87 bp的序列与另一个MVAT VSG基因的启动子相似,但并不相同。紫外线照射实验用于检测在表达不相关VSG的血流锥虫中,来自这个MVAT5启动子的RNA合成情况。我们认为,这个序列是MVAT5 VSG mRNA的特异性启动子,在寄生虫生命周期的循环后期阶段,约10%的锥虫群体中会出现这种mRNA。