Azuara-Liceaga E, Flores-Soto E, López-Camarillo C, Orozco E
Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, San Lorenzo # 290, Col. Del Valle, CP 03100, Mexico D.F., Mexico.
Exp Parasitol. 2005 Jul;110(3):280-5. doi: 10.1016/j.exppara.2005.03.004. Epub 2005 Apr 11.
The Entamoeba histolytica Ehcp112 and Ehadh112 genes that encode the EhCPADH complex are separated by a non-coding 188pb region. Their proximity suggests a coordinated expression regulation for both genes. Here, we studied the structure and function of 996 bp (p996CAT) upstream the ATG start codon of the Ehadh112 gene. The p996CAT plasmid drove CAT transcription with a 78% of the activity showed by actin promoter. Deletion of 330 bp at the 5' end of p966CAT to produce the p776CAT plasmid, decreased activity to 40% in relation to actin promoter and to 50% of p996CAT, suggesting the presence of a silencer in this region. Interestingly, deletion of other 297 bp to the p776CAT to generate the p469CAT plasmid, augmented activity in 2.5-fold compared with p776CAT construction, showing the presence of a proximal enhancer promoter. Transcription initiation sites (-69 and -150 bp), TATA like box, GAAC, and Inr elements, as well as putative DNA binding motifs, were mapped in the -1 to -469 bp core promoter region.
编码EhCPADH复合物的溶组织内阿米巴Ehcp112和Ehadh112基因被一个188pb的非编码区域隔开。它们的相邻关系表明这两个基因存在协调的表达调控。在此,我们研究了Ehadh112基因ATG起始密码子上游996bp(p996CAT)的结构和功能。p996CAT质粒驱动CAT转录,其活性为肌动蛋白启动子所显示活性的78%。在p966CAT的5'端缺失330bp以产生p776CAT质粒,相对于肌动蛋白启动子,活性降低至40%,相对于p996CAT降低至50%,这表明该区域存在一个沉默子。有趣的是,在p776CAT上再缺失另外297bp以产生p469CAT质粒,与p776CAT构建体相比,活性增加了2.5倍,表明存在一个近端增强子启动子。转录起始位点(-69和-150bp)、类TATA盒、GAAC和Inr元件以及假定的DNA结合基序,被定位在-1至-469bp的核心启动子区域。