Pays E, Tebabi P, Pays A, Coquelet H, Revelard P, Salmon D, Steinert M
Department of Molecular Biology, Free University of Brussels, Belgium.
Cell. 1989 Jun 2;57(5):835-45. doi: 10.1016/0092-8674(89)90798-8.
The AnTat 1.3A antigen gene expression site of T. brucei was cloned from genomic libraries of the 200 kb expressor chromosome. In addition to the antigen gene, it contains seven putative coding regions (ESAGs, for expression site-associated genes), as well as a RIME retroposon. The polypeptide encoded by ESAG 4 shows homology to yeast adenylate cyclase, and possesses structural features of a transmembrane protein. The expression site is transcribed by a pol l-like polymerase in the parasite bloodstream form only, but sequences similar to ESAGs 5, 4, and 2 are also transcribed constitutively elsewhere, by a polymerase sensitive to alpha-amanitin. Ultraviolet irradiation, which seems to block RNA processing, allows the tentative mapping of a transcription promoter about 45 kb upstream of the antigen gene.
布氏锥虫的AnTat 1.3A抗原基因表达位点是从200 kb表达染色体的基因组文库中克隆出来的。除了抗原基因外,它还包含七个推定的编码区(ESAGs,即表达位点相关基因)以及一个RIME反转录转座子。ESAG 4编码的多肽与酵母腺苷酸环化酶具有同源性,并具有跨膜蛋白的结构特征。该表达位点仅在寄生虫血流形式中由类似pol l的聚合酶转录,但与ESAGs 5、4和2相似的序列在其他地方也由对α-鹅膏蕈碱敏感的聚合酶组成性转录。紫外线照射似乎会阻断RNA加工,从而使我们能够初步定位抗原基因上游约45 kb处的转录启动子。