Harrison D G, Venema R C, Arnal J F, Inoue N, Ohara Y, Sayegh H, Murphy T J
Department of Medicine, Emory University of Medicine, Atlanta, GA.
Agents Actions Suppl. 1995;45:107-17. doi: 10.1007/978-3-0348-7346-8_16.
During the past two years, the enzyme responsible for production of endothelium-derived nitric oxide, the endothelial cell NO synthase (ecNOS) has been cloned and the gene encoding this enzyme isolated, cloned and its structure characterized. This research has provided direction for a variety of studies of regulation of the ecNOS. Several features of the ecNOS are compatible with a constitutively expressed, poorly regulated gene, including absence of a TATA box and numerous SP-1 sites. The promoter also contains a number of putative binding domains which suggest that it may be regulated by a variety of transcription factor mediated signals. In this review we will discuss evidence to support the concept that the ecNOS is a constitutively expressed gene subject to a modest degree of regulation by important physiological influences.
在过去两年中,负责产生内皮衍生一氧化氮的酶——内皮细胞一氧化氮合酶(ecNOS)已被克隆,编码该酶的基因也已被分离、克隆并确定其结构特征。这项研究为ecNOS调节的各种研究提供了方向。ecNOS的几个特征与一个组成性表达、调节不佳的基因相符,包括缺乏TATA框和众多SP-1位点。该启动子还包含一些假定的结合域,这表明它可能受多种转录因子介导的信号调节。在这篇综述中,我们将讨论支持以下概念的证据:ecNOS是一个组成性表达的基因,受到重要生理影响的适度调节。