Morishita K, Tsuchiya M, Asano S, Kaziro Y, Nagata S
Institute of Medical Science, University of Tokyo, Japan.
J Biol Chem. 1987 Nov 5;262(31):15208-13.
By using the full-length cDNA as a probe, the chromosomal gene for human myeloperoxidase was isolated from a human gene library. Comparison of the nucleotide sequence of the chromosomal gene with that of the cDNA has revealed that the human myeloperoxidase gene is composed of 12 exons and 11 introns. S1 mapping analysis of human myeloperoxidase mRNA identified the single transcription initiation site at 180 base pairs upstream of the ATG initiation codon. In the 5'-flanking region of the human myeloperoxidase gene, there are several blocks of sequences which are homologous to the sequences found on the 5'-promoter region of the human c-myc proto-oncogene. The myeloperoxidase gene is expressed in mouse myeloid leukemia WEHI-3B D+ and NFS-60 cells. When these cells were treated with human recombinant granulocyte colony-stimulating factor, the steady-state level of myeloperoxidase mRNA declined to zero within 36 h in WEHI-3B D+ cells, but not in NFS-60 cells.
以全长cDNA为探针,从人基因文库中分离出人类髓过氧化物酶的染色体基因。将染色体基因的核苷酸序列与cDNA的核苷酸序列进行比较,结果表明人类髓过氧化物酶基因由12个外显子和11个内含子组成。对人类髓过氧化物酶mRNA的S1定位分析确定了位于ATG起始密码子上游180个碱基对处的单一转录起始位点。在人类髓过氧化物酶基因的5'侧翼区域,有几个序列块与人类c-myc原癌基因5'启动子区域发现的序列同源。髓过氧化物酶基因在小鼠髓性白血病WEHI-3B D+和NFS-60细胞中表达。当用人类重组粒细胞集落刺激因子处理这些细胞时,WEHI-3B D+细胞中髓过氧化物酶mRNA的稳态水平在36小时内降至零,而NFS-60细胞中则没有。