Shinoda T
National Chemical Laboratory for Industry, Tsukuba Research Center, Ibaraki, Japan.
Nucleic Acids Symp Ser. 1992(27):173-4.
The base sequence of a specific DNA region of the APP gene identified as the promoter was analyzed by means of the quantity Sr corresponding to superdelocalizability of oxygen ion of each phosphate for the ten DNA dimer units (XY/Y' X') and the six [(XY/Y'X')+H+] complexes. The base sequence of the -35 signal was determined to be 5'-CAGCTG-3' (-49 to -44). On the other hand, the base sequence of the -10 signal was found several ones. Therefore, transcription is to initiate at multiple sites. The mechanisum how RNA polymerases can recognize each transcription site, was proposed. The result explains fairly well some characteristics of the promoter of the APP gene experimentally found so far.
通过对十个DNA二聚体单元(XY/Y'X')和六个[(XY/Y'X')+H+]复合物中每个磷酸根氧离子的超离域性对应的量Sr,分析了被鉴定为启动子的APP基因特定DNA区域的碱基序列。确定-35信号的碱基序列为5'-CAGCTG-3'(-49至-44)。另一方面,发现了几个-10信号的碱基序列。因此,转录在多个位点起始。提出了RNA聚合酶如何识别每个转录位点的机制。该结果很好地解释了迄今为止实验发现的APP基因启动子的一些特征。