Chrapkiewicz N B, Davis C M, Chu D T, Caldwell C M, Granner D K
Department of Molecular Physiology and Biophysics, Vanderbilt University Medical School, Nashville, TN 37232.
Nucleic Acids Res. 1989 Aug 25;17(16):6651-67. doi: 10.1093/nar/17.16.6651.
Several overlapping cDNA and genomic DNA clones corresponding to mRNA g33 and gene 33, respectively, were isolated and characterized. The mRNA g33 molecule is 2971 nt in length, exclusive of a poly(A+) tail, and encodes a putative 459 amino acid protein (49,946 daltons). The 13.2 kbp gene consists of four exons, three introns, and has two initiation sites located 27 and 30 bp downstream from a TATA box. Transfection of H4IIE cells with a fusion gene 33 (-1900 to +32)/luciferase construct (pSL330A) gave rise to readily detectable luciferase activity. In addition, primer extension analysis of the gene 33/luciferase mRNA transcribed in these experiments showed that transcription initiates in the gene 33 DNA at two sites consistent with those found in vivo. Analysis of the effect of 5' deletions on basal promoter activity showed that, in relation to the promoter activity of pSL330A, approximately 40% of the activity is lost between -1643 and -1050, another approximately 40% between -550 and -475, and deletion to -55 causes a total loss of detectable luciferase activity.
分别分离并鉴定了几个与mRNA g33和基因33相对应的重叠cDNA和基因组DNA克隆。mRNA g33分子长度为2971 nt(不包括聚腺苷酸尾),编码一种推定的459个氨基酸的蛋白质(49,946道尔顿)。这个13.2 kbp的基因由四个外显子、三个内含子组成,并且在TATA框下游27和30 bp处有两个起始位点。用融合基因33(-1900至+32)/荧光素酶构建体(pSL330A)转染H4IIE细胞后产生了易于检测到的荧光素酶活性。此外,对这些实验中转录的基因33/荧光素酶mRNA进行引物延伸分析表明,转录在基因33 DNA中的两个位点起始,这与体内发现的位点一致。对5'缺失对基础启动子活性的影响分析表明,相对于pSL330A的启动子活性,在-1643和-1050之间大约损失了40%的活性,在-550和-475之间又损失了大约40%,缺失至-55会导致可检测到的荧光素酶活性完全丧失。