Serventi I M, Cavanaugh E, Moss J, Vaughan M
Laboratory of Cellular Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Mar 5;268(7):4863-72.
ADP-ribosylation factors (ARFs) are a family of approximately 20-kDa guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activities of cholera toxin in vitro and function in protein trafficking in vivo. The six cloned mammalian ARFs can be grouped into three classes based on size and sequence identity. ARF 2 is a class I ARF, whose approximately 2.6-kilobase mRNA exhibits species and tissue selective expression and is developmentally regulated in rat brain. Here we report the sequence, structure, and functional promoter region of the bovine ARF 2 gene, which was facilitated by constructing a composite cDNA. The ARF 2 cDNA, constructed from a partial cDNA clone and polymerase chain reaction-amplified fragments from reverse-transcribed poly(A)+ RNA, was approximately 2270 base pairs (bp) (minus the poly(A) tail). In the 3'-untranslated region, there are two potential polyadenylation signals, ATTAAA and AATAAA, at positions 1064 and 2232, respectively, and two ATTTA motifs, believed to signal mRNA degradation, at positions 2115 and 2165. The ARF 2 gene, represented in three overlapping genomic clones, spans approximately 20 kilobase pairs with five exons and four introns. Consensus sequences for guanine nucleotide-binding and GTP hydrolysis are in separate exons, except for the NKXD sequence, which is divided by intron 4. There are multiple transcriptional initiation sites. Transient transfection of embryonic trachea cells with deletion constructs defined the functional promoter region to be within 400 bp upstream of the most 5' site of transcription initiation. This 400-bp region lacks a TATA-like sequence but contains six inverted CCAAT boxes, four potential Sp1-binding sites, and a potential AP-2-binding site. Although the pattern of expression of ARF 2 is unique among the ARFs, the structures of the class I ARF genes are conserved among its members and across species.
ADP-核糖基化因子(ARFs)是一类分子量约为20 kDa的鸟嘌呤核苷酸结合蛋白,在体外可刺激霍乱毒素的ADP-核糖基转移酶活性,在体内参与蛋白质转运。根据大小和序列同源性,已克隆的6种哺乳动物ARFs可分为三类。ARF 2属于I类ARF,其约2.6千碱基的mRNA呈现物种和组织选择性表达,且在大鼠脑中受发育调控。在此,我们报告牛ARF 2基因的序列、结构和功能启动子区域,这得益于构建一个复合cDNA。由一个部分cDNA克隆和逆转录的聚腺苷酸加尾RNA经聚合酶链反应扩增片段构建的ARF 2 cDNA约为2270个碱基对(bp)(不含聚腺苷酸尾)。在3'非翻译区,分别在第1064位和第2232位有两个潜在的聚腺苷酸化信号ATTAAA和AATAAA,在第2115位和第2165位有两个ATTTA基序,被认为是mRNA降解的信号。ARF 2基因由三个重叠的基因组克隆代表,跨度约20千碱基对,有五个外显子和四个内含子。除了被内含子4分隔的NKXD序列外,鸟嘌呤核苷酸结合和GTP水解的共有序列位于不同的外显子中。有多个转录起始位点。用缺失构建体对胚胎气管细胞进行瞬时转染,确定功能启动子区域位于转录起始最5'位点上游400 bp内。这个400 bp的区域缺乏类似TATA的序列,但包含六个反向CCAAT框、四个潜在的Sp1结合位点和一个潜在的AP-2结合位点。尽管ARF 2的表达模式在ARFs中是独特的,但I类ARF基因的结构在其成员之间以及跨物种中是保守的。