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人源细胞内物质转运调节分子ARFGAP1对细胞分泌功能的影响
引用本文:刘晓勤,张成岗,邢桂春,陈清棠,贺福初.人源细胞内物质转运调节分子ARFGAP1对细胞分泌功能的影响[J].中国生物化学与分子生物学报,2001,17(2):237-243.
作者姓名:刘晓勤  张成岗  邢桂春  陈清棠  贺福初
作者单位:1. 军事医学科学院放射医学研究所;北京大学第一医院神经内科
2. 军事医学科学院放射医学研究所
3. 北京大学第一医院神经内科
基金项目:国家自然科学基金项目(No.39730310和30070386)
摘    要: ARF GAP是重要的细胞内物质转运调节分子 .最近 ,在人胎肝 c DNA文库中发现一种新基因 ,其编码的氨基酸序列与大鼠的 ARF1 GAP有 32 %同源性 ,故将其命名为“ARFGAP1”.对ARFGAP1进行功能研究 ,利用分子克隆技术构建绿色荧光蛋白 (GFP) - ARFGAP1融合基因表达质粒 (p EGFP- C1 - ARFGAP1 ) ,经脂质体转染将其导入 COS- 7细胞瞬时表达 ,利用绿色荧光确定ARFGAP1的亚细胞定位 .结果显示 ,ARFGAP1位于细胞质部分 ,表达量高时 ,在核周高尔基体区聚集呈团块状或颗粒状 .构建真核表达质粒 pc DNA3.1 /myc- His- ARFGAP1 ,在 COS- 7细胞中表达 ,并用 ARFGAP1和分泌型碱性磷酸酶 (SEAP)真核表达质粒共同转染 COS- 7细胞 ,发现ARFGAP1在细胞中过表达能部分抑制 SEAP的分泌 .结果证明 ,ARFGAP1对细胞的物质转运和分泌功能有调节作用 .

关 键 词:ADP核糖基化因子  GTP酶活化蛋白  亚细胞定位  分泌型碱性磷酸酶
收稿时间:2001-04-20
修稿时间:2000年7月27日

Effect of ARFGAP1,a Human-derived Regulator of Intracellular Transport,on Cellular Secretory Function
LIU Xiao\|qin,ZHANG Cheng gang ,XING Gui\|chun ,CHEN Qing\|tang ,HE Fu\|chu.Effect of ARFGAP1,a Human-derived Regulator of Intracellular Transport,on Cellular Secretory Function[J].Chinese Journal of Biochemistry and Molecular Biology,2001,17(2):237-243.
Authors:LIU Xiao\|qin    ZHANG Cheng gang  XING Gui\|chun  CHEN Qing\|tang  HE Fu\|chu
Institution:( 1) Institute of Radiation Medicine,Academy of Military Medical Sciences,Beijing\ 100850,China; 2) Department of Neu
Abstract:ADP\|ribosylation factors(ARFs)are critical components in vesicular trafficking pathways,which are active in their GTP\|bound form and controlled by GTPase\|activating proteins(GAPs).ARF GAPs are important regulators of intracellular transport.Recently,a novel human gene was cloned from a cDNA library of second trimester human fetal liver.The amino acid sequence encoded by the novel gene has 32% similarity to rat ARF1 GAP and is thus termed as ARFGAP1.The functional characterization of the new gene was studied.The recombinant expression plasmid pEGFP\|Cl\|ARFGAP1 tagged with green fluorescence protein(GFP)was constructed by routine molecular cloning technique.pEGFP\|Cl\|ARFGAP1 was transfected into COS\|7 cells by lipofectin reagent.The transient expression of GFP\|ARFGAP1 fusion protein in COS\|7 was confirmed by Western blotting analysis.Subcellular localization of ARFGAP1 in COS\|7 was determined by fluorescence microscope.The result showed that ARFGAP1 was localized in vesicular structures that are concentrated mainly in the perinuclear region.but were also found throughout the cytosol.Moreover,the recombinant expression plasmid pcDNA 3 1/myc\|His\|ARFGAP1 was constructed and transfected into COS\|7 cells.The expression of ARFGAP1 was verified by Western blotting analysis.It was found that the overexpression of ARFGAP1 in cultured cells reduced the constitutive secretion of secreted form of alkaline phosphatase(SEAP) partly and reproducibly by co\|transfecting COS\|7 cells with pcDNA3.1/myc\|His\|ARFGAP1 and pGEM\|SEAP.It is proposed that ARFGAP1 be involoved in regulation of intracellular transport and cellular secretion.
Keywords:ADP\|ribosylation factor(ARF)  GTPase activating protein(GAP)  subcellular localization  secreted alkaline phosphatase
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