Yasuda T, Nadano D, Iida R, Takeshita H, Lane S A, Callen D F, Kishi K
Department of Legal Medicine, Fukui Medical School, Japan.
Cytogenet Cell Genet. 1995;70(3-4):221-3. doi: 10.1159/000134038.
To localize the human deoxyribonuclease I (DNase I) gene, DNASE1 (DNL1), we performed a polymerase chain reaction (PCR) using DNA extracted from a panel of cloned human x rodent hybrid cell lines carrying different human chromosomes and screened for the presence of the expected PCR products. Two different sets of oligonucleotide primers specific for human DNase I cDNA sequences were used to amplify unique fragments in the human DNase I gene. Based on this work, DNL1 could be assigned to human chromosome 16. Furthermore, regional localization of the gene to 16p13.3 was performed by PCR analysis of a high-resolution mouse x human somatic cell hybrid panel that contained defined portions of human chromosome 16.
为了定位人类脱氧核糖核酸酶I(DNase I)基因DNASE1(DNL1),我们使用从一组携带不同人类染色体的克隆人-啮齿动物杂交细胞系中提取的DNA进行了聚合酶链反应(PCR),并筛选预期PCR产物的存在情况。使用两组不同的针对人类DNase I cDNA序列的寡核苷酸引物来扩增人类DNase I基因中的独特片段。基于这项工作,DNL1可被定位到人类16号染色体。此外,通过对包含人类16号染色体特定部分的高分辨率小鼠-人类体细胞杂交细胞系进行PCR分析,将该基因定位到16p13.3区域。