Ben Amar M F, Jefferies D, Pays A, Bakalara N, Kendall G, Pays E
Department of Molecular Biology, University of Brussels, Belgium.
Nucleic Acids Res. 1991 Nov 11;19(21):5857-62. doi: 10.1093/nar/19.21.5857.
The actin genes of Trypanosoma brucei are transcribed constitutively during the parasite life-cycle, by a polymerase sensitive to alpha-amanitin. The start region of the actin gene transcription unit was mapped by virtue of the accumulation of promoter-proximal transcripts which occurs following moderate UV irradiation. This region, located about 4 kilobases upstream from the genes, was able to direct transient expression of the bacterial Chloramphenicol Acetyl Transferase (CAT) gene in both bloodstream and procyclic forms of the parasite. The essential region of the promoter was defined by deletion, and appeared to be within 600 bp upstream from the putative transcription start site. It does not share significant homology with the other trypanosome promoters described so far (VSG, procyclin, rDNA), which all direct alpha-amanitin resistant transcription.
布氏锥虫的肌动蛋白基因在寄生虫生命周期中由对α-鹅膏蕈碱敏感的聚合酶持续转录。通过中度紫外线照射后启动子近端转录本的积累,绘制了肌动蛋白基因转录单位的起始区域。该区域位于基因上游约4千碱基处,能够在寄生虫的血流型和前循环型中指导细菌氯霉素乙酰转移酶(CAT)基因的瞬时表达。启动子的必需区域通过缺失来定义,似乎位于假定转录起始位点上游600 bp内。它与迄今为止描述的其他锥虫启动子(VSG、前环蛋白、rDNA)没有显著同源性,这些启动子都指导对α-鹅膏蕈碱抗性的转录。