Coquelet H, Tebabi P, Pays A, Steinert M, Pays E
Department of Molecular Biology, University of Brussels, Rhode-Saint-Genèse, Belgium.
Mol Cell Biol. 1989 Sep;9(9):4022-5. doi: 10.1128/mcb.9.9.4022-4025.1989.
The expression site for the variable surface glycoprotein (VSG) gene AnTat 1.3A of Trypanosoma brucei is 45 kilobases long and encompasses seven expression site-associated genes (ESAGs) (E. Pays, P. Tebabi, A. Pays, H. Coquelet, P. Revelard, D. Salmon, and M. Steinert, Cell 57:835-845, 1989). After UV irradiation, several large transcripts from the putative promoter region were strongly enriched. We report that one such major transcript starts near the poly(A) addition site of the first gene (ESAG 7), spans the intergenic region, and extends to the poly(A) addition site of the second gene (ESAG 6), thus bypassing the normal 3' splice site of the ESAG 6 mRNA. Since this transcript is spliced, we conclude that UV irradiation does not inhibit splicing but stabilizes unstable processing products. This demonstrates that at least some intergenic regions of the VSG gene expression site are continuously transcribed in accordance with a polycistronic transcription model.
布氏锥虫可变表面糖蛋白(VSG)基因AnTat 1.3A的表达位点长45千碱基,包含7个表达位点相关基因(ESAGs)(E. Pays、P. Tebabi、A. Pays、H. Coquelet、P. Revelard、D. Salmon和M. Steinert,《细胞》57:835 - 845,1989年)。紫外线照射后,来自假定启动子区域的几个大转录本大量富集。我们报告,这样一个主要转录本起始于第一个基因(ESAG 7)的多聚腺苷酸化位点附近,跨越基因间区域,并延伸至第二个基因(ESAG 6)的多聚腺苷酸化位点,从而绕过了ESAG 6 mRNA正常的3'剪接位点。由于这个转录本被剪接,我们得出结论,紫外线照射并不抑制剪接,而是稳定了不稳定的加工产物。这表明VSG基因表达位点的至少一些基因间区域按照多顺反子转录模型持续转录。