Zhang J, Tan C K, McMullen B, Downey K M, So A G
Department of Medicine, University of Miami School of Medicine, Florida 33101, USA.
Genomics. 1995 Sep 1;29(1):179-86. doi: 10.1006/geno.1995.1229.
cDNAs encoding the small subunit of bovine and human DNA polymerase delta have been cloned and sequenced. The predicted polypeptides, 50,885 and 51,289 Daltons, respectively, are 94% identical, similar to the catalytic subunits. The high degree of conservation of the polypeptides suggests an essential function for the small subunit in the heterodimeric core enzyme. Although the catalytic subunit of DNA polymerase delta shares significant homology with those of the herpes virus family of DNA polymerases, the small subunit of mammalian DNA polymerase delta is not homologous to the small subunit of either herpes simplex virus type 1 DNA polymerase (UL42 protein) or the Epstein-Barr virus DNA polymerase (BMRF1 protein). Searches of the protein databases failed to detect significant homology with any protein sequenced thus far. PCR analysis of DNA from a panel of human-hamster hybrid cell lines localized the gene (POLD2) for the small subunit of DNA polymerase delta to human chromosome 7.
编码牛和人DNA聚合酶δ小亚基的cDNA已被克隆和测序。预测的多肽分别为50,885和51,289道尔顿,与催化亚基相似,二者有94%的同一性。多肽的高度保守性表明小亚基在异二聚体核心酶中具有重要功能。尽管DNA聚合酶δ的催化亚基与疱疹病毒DNA聚合酶家族的催化亚基有显著同源性,但哺乳动物DNA聚合酶δ的小亚基与单纯疱疹病毒1型DNA聚合酶(UL42蛋白)或爱泼斯坦-巴尔病毒DNA聚合酶(BMRF1蛋白)的小亚基均不同源。在蛋白质数据库中搜索未发现与目前已测序的任何蛋白质有显著同源性。对一组人-仓鼠杂交细胞系的DNA进行PCR分析,将DNA聚合酶δ小亚基的基因(POLD2)定位到人类染色体7上。