Rao C D, Igarashi H, Chiu I M, Robbins K C, Aaronson S A
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2392-6. doi: 10.1073/pnas.83.8.2392.
The structure of the normal human c-sis/platelet-derived growth factor 2 (SIS/PDGF2) transcript was determined by a combination of cDNA cloning, nuclease S1 mapping, and primer extension. Nucleotide sequence analysis revealed that the 3373-nucleotide SIS/PDGF2 mRNA contained only a 723-base-pair (bp) coding sequence for the PDGF2 precursor polypeptide. The coding sequence was flanked by long 5' (1022 bp) and 3' (1625 bp) untranslated regions. The 5' noncoding region, as well as upstream flanking genomic sequences, contained clusters of specific short repeat sequences. A consensus transcriptional promoter sequence, TATAAA, was identified 24 bp upstream of the mRNA start site and an enhancer-like "TG element" was detected about 180 bp downstream from the site of polyadenylylation. These findings identify putative regulatory elements of the SIS/PDGF2 gene.
通过cDNA克隆、核酸酶S1图谱分析和引物延伸相结合的方法,确定了正常人c-sis/血小板衍生生长因子2(SIS/PDGF2)转录本的结构。核苷酸序列分析表明,3373个核苷酸的SIS/PDGF2 mRNA仅包含一个723个碱基对(bp)的PDGF2前体多肽编码序列。编码序列两侧是长的5'(1022 bp)和3'(1625 bp)非翻译区。5'非编码区以及上游侧翼基因组序列包含特定短重复序列簇。在mRNA起始位点上游24 bp处鉴定出一个共有转录启动子序列TATAAA,在多聚腺苷酸化位点下游约180 bp处检测到一个增强子样的“TG元件”。这些发现确定了SIS/PDGF2基因的假定调控元件。