Zhang Jia, Zhang Weiping, Zou Dajin, Chen Guoyou, Wan Tao, Zhang Minghui, Cao Xuetao
Institute of Immunology and Department of Internal Medicine, Second Military Medical University, 800 Xiangyin Road, 200433, Shanghai, P.R. China.
J Cancer Res Clin Oncol. 2003 Feb;129(2):76-83. doi: 10.1007/s00432-002-0413-7. Epub 2003 Mar 1.
To identify the biological function of a novel molecule which shows high homology with human guanosine monophosphate reductase (GMPR) and is named GMPR2.
GMPR2 cDNA was cloned from the cDNA library of human dendritic cells and was characterized by Bioinformatics. The expression pattern of GMPR2 was analyzed by Northern blotting. The enzymatic activity of the purified recombinant GMPR2 protein was determined using a spectrophotometric assay. HL-60 leukemia cells were transfected with GMPR2 and the expression of CD14 and myeloperoxidase (MPO) in HL-60 cells with and without 12- o-tetra-decanoyl-phorbol-13-acetate (TPA) induction was monitored by FACS analysis.
The novel gene contained ten exons and nine introns and was mapped to 14q11-21. Northern blotting indicated a ubiquitous expression of GMPR2 mRNA in most of the human tissues and cancer cell lines investigated. The recombinant GMPR2 protein was able to reduce GMP. The expression of CD14 and MPO in HL-60 leukemia cells overexpressing GMPR2 clearly increased after induction by TPA.
GMPR2 is a novel human GMP reductase, and overexpression of GMPR2 can promote the monocytic differentiation of HL-60 leukemia cells.
鉴定一种与人类鸟苷单磷酸还原酶(GMPR)具有高度同源性且命名为GMPR2的新型分子的生物学功能。
从人树突状细胞的cDNA文库中克隆GMPR2 cDNA,并通过生物信息学进行表征。通过Northern印迹分析GMPR2的表达模式。使用分光光度法测定纯化的重组GMPR2蛋白的酶活性。用GMPR2转染HL-60白血病细胞,并通过流式细胞术分析监测HL-60细胞在有和没有12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导的情况下CD14和髓过氧化物酶(MPO)的表达。
该新基因包含10个外显子和9个内含子,定位于14q11-21。Northern印迹表明,在大多数研究的人类组织和癌细胞系中,GMPR2 mRNA普遍表达。重组GMPR2蛋白能够还原GMP。在TPA诱导后,过表达GMPR2的HL-60白血病细胞中CD14和MPO的表达明显增加。
GMPR2是一种新型的人类GMP还原酶,GMPR2的过表达可促进HL-60白血病细胞的单核细胞分化。