Hug M, Carruthers V B, Hartmann C, Sherman D S, Cross G A, Clayton C
Zentrum für Molekulare Biologie, Heidelberg, Germany.
Mol Biochem Parasitol. 1993 Sep;61(1):87-95. doi: 10.1016/0166-6851(93)90161-p.
A series of Trypanosoma brucei transfection vectors was constructed in which transcription of the luciferase gene was driven by the procyclic acidic repetitive protein (procyclin) promoter. The untranslated regions surrounding the luciferase gene were derived from the actin, fructose bisphosphate aldolase, or PARP loci. Trans-splicing of the resulting transcripts occurred as expected, but the site of 3' polyadenylation was upstream of the position anticipated. The nature of the 3'-untranslated region was crucial to the level of expression in bloodstream forms.
构建了一系列布氏锥虫转染载体,其中荧光素酶基因的转录由前循环酸性重复蛋白(前循环素)启动子驱动。荧光素酶基因周围的非翻译区来自肌动蛋白、果糖二磷酸醛缩酶或聚(ADP-核糖)聚合酶基因座。所得转录本的反式剪接如预期发生,但3'聚腺苷酸化位点位于预期位置的上游。3'非翻译区的性质对于血流形式中的表达水平至关重要。