Chernak J M
Molecular Neurobiology Unit, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224.
Gene. 1993 Nov 15;133(2):255-60. doi: 10.1016/0378-1119(93)90648-m.
The 5' upstream regulatory region of the gene encoding the rat amyloid precursor protein (APP) was cloned and sequenced. It lacks both a TATA box and a CAAT box, has a high G + C content (68%), is 89% homologous to the corresponding region of the mouse APP gene, and 82% homologous to the corresponding region of the human APP gene. This region contains putative regulatory elements both 5' and 3' to the probable transcription start point (tsp). There are consensus DNA sites for the binding of SP1, AP2, AP4 and GC factor (GCF) proteins, and two GC boxes with the consensus sequence, 5'-GGGYGCRG. Potential regulatory sites with only a single mismatch to the consensus sequences include three SP1, one AP1, five AP2, and two GCF sites, as well as one GC box. There are also six potential stem-loop secondary structures (SSS) near the probable tsp. A consecutive series of elements, consisting of a GC box, AP2 site, three SSS, two SP1 sites, and AP4, AP1 and GCF sites just upstream from the probable tsp, are well-conserved between the rat, mouse and human sequences. An additional AP2 site, two GC boxes, and two additional SSS appear to be conserved between species. However, two possible rat SP1 sites, three possible rat AP2 sites, and two possible rat GCF sites are lacking in the human. On the other hand, the rat sequence is missing four potential SP1 sites, four potential AP2 sites, and nine potential GC boxes which are found in the human sequence.(ABSTRACT TRUNCATED AT 250 WORDS)
编码大鼠淀粉样前体蛋白(APP)的基因的5'上游调控区域被克隆并测序。它既缺乏TATA盒也缺乏CAAT盒,G + C含量高(68%),与小鼠APP基因的相应区域有89%的同源性,与人类APP基因的相应区域有82%的同源性。该区域在可能的转录起始点(tsp)的5'和3'端都包含推定的调控元件。存在用于SP1、AP2、AP4和GC因子(GCF)蛋白结合的共有DNA位点,以及两个具有共有序列5'-GGGYGCRG的GC盒。与共有序列仅有一个错配的潜在调控位点包括三个SP1、一个AP1、五个AP2和两个GCF位点,以及一个GC盒。在可能的tsp附近还有六个潜在的茎环二级结构(SSS)。在大鼠、小鼠和人类序列之间,由一个GC盒、AP2位点、三个SSS、两个SP1位点以及恰好在可能的tsp上游的AP4、AP1和GCF位点组成的一系列连续元件高度保守。另外一个AP2位点、两个GC盒和另外两个SSS似乎在物种间保守。然而,人类中缺少两个可能的大鼠SP1位点、三个可能的大鼠AP2位点和两个可能的大鼠GCF位点。另一方面,大鼠序列中缺少人类序列中发现的四个潜在SP1位点、四个潜在AP2位点和九个潜在GC盒。(摘要截短于250字)