Strijker R, Blom van Assendelft G, Dikkeschei B D, Gruber M, Ab G
Gene. 1986;45(1):27-35. doi: 10.1016/0378-1119(86)90128-9.
We have investigated RNAs originating from the 5'-flanking region of the chicken very-low-density apolipoprotein II (apoVLDLII) gene. S1 nuclease mapping and primer extension experiments revealed two minor upstream transcription start points located 1105 and 1530 nucleotides in front of the apoVLDLII gene. Transcription starting at these points is dependent upon estradiol as is transcription from the major start points. The transcripts are polyadenylated, but are not detectable in polysomes. Run-on assays indicated that the low concentration of the upstream initiated transcripts is due both to low transcription levels and to low transcript stability. The sequence around the upstream start points does not show strong homologies with consensus sequences of promoters for eukaryotic protein encoding genes. Nevertheless, the upstream sequences are transcribed in vivo by RNA polymerase II.
我们研究了源自鸡极低密度载脂蛋白II(apoVLDLII)基因5'侧翼区域的RNA。S1核酸酶图谱分析和引物延伸实验揭示了apoVLDLII基因前1105和1530个核苷酸处的两个次要上游转录起始点。从这些位点起始的转录依赖于雌二醇,就像从主要起始点的转录一样。这些转录本进行了多聚腺苷酸化,但在多核糖体中无法检测到。连续转录分析表明,上游起始转录本的低浓度是由于低转录水平和低转录本稳定性。上游起始点周围的序列与真核蛋白质编码基因启动子的共有序列没有很强的同源性。然而,上游序列在体内由RNA聚合酶II转录。