Szabo P, Panneerselvam C, Clinton M, Frangou-Lazaridis M, Weksler D, Whittington E, Macera M J, Grzeschik K H, Selvakumar A, Horecker B L
Department of Medicine, Cornell University Medical College, New York, NY 10021.
Hum Genet. 1993 Feb;90(6):629-34. doi: 10.1007/BF00202480.
A genomic clone encoding prothymosin alpha (gene symbol: PTMA), a nuclear-targeted protein associated with cell proliferation, was isolated and the 5'-regulatory region subcloned and sequenced. Because of previously reported discrepancies between several cDNA clones and a genomic clone for prothymosin alpha, we determined the sequence of the first exon and of a 1.7-kb region 5' to the first exon. The sequence of the genomic clone reported here corresponds to the published cDNA sequences, suggesting that the previously noted discrepancies may be due to genetic polymorphism in this region. In addition, our sequence data extend the known 5'-upstream sequence by an additional 1.5 kb allowing the identification of numerous, potential cis-acting regulatory sites. This 5'-flanking cloned probe permitted us to localize the prothymosin gene to chromosome 2 in humans.
一个编码前胸腺素α(基因符号:PTMA)的基因组克隆被分离出来,该蛋白是一种与细胞增殖相关的核靶向蛋白。然后将5'调控区亚克隆并测序。由于先前报道的几个前胸腺素α的cDNA克隆与基因组克隆之间存在差异,我们测定了第一个外显子以及第一个外显子上游1.7 kb区域的序列。此处报道的基因组克隆序列与已发表的cDNA序列一致,这表明先前指出的差异可能是由于该区域的基因多态性。此外,我们的序列数据将已知的5'上游序列又延伸了1.5 kb,从而能够鉴定出许多潜在的顺式作用调控位点。这个5'侧翼克隆探针使我们能够将前胸腺素基因定位到人类的2号染色体上。