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小鼠ZnT3 cDNA片断的克隆及其mRNA表达
引用本文:龙建纲,王福俤,陈坚,沈慧,王海明,张元勋.小鼠ZnT3 cDNA片断的克隆及其mRNA表达[J].卫生研究,2002,31(2):103-105.
作者姓名:龙建纲  王福俤  陈坚  沈慧  王海明  张元勋
作者单位:1. 第二军医大学军队卫生学教研室,上海,200433
2. 中科院核技术分析开放研究实验室,上海,201800
基金项目:国家自然科学基金 (No.39770 643,39970 641,30 1 70 80 5,1 0 1 750 85),军队“九五”青年基金 (No .98Q0 4 3),中科院核分析技术开放研究实验室基金
摘    要:为了解ZnT3(zinc transporter3)mRNA在小鼠各组织中的表达状况,用反转录多聚酶链反应法(RTPCR)克隆ZnT3 cDNA片段,荧光标记的全自动测序法确定ZnT3 cDNA片断的减基顺序,RT-PCR法检测小鼠各组织ZnT3mRNA表达并比较在组织中的表达量,结果:RT-PCR获得单一条带的片断,其大小700bp,碱基顺序与文献报道序列一致,在大脑皮层,海马和睾丸中检测到ZnT3 mRNA表达,其中睾丸中表达量最高,大脑皮层,海马表达量无显著性差别,心,肝脾,肺,肾,小肠及嗅球,小脑等组织中未见ZnT3 mRNA表达,说明克隆到正确的ZnT3 cDNA片断,ZnT3 mRNA主要表达于睾丸,大脑皮层,海马,提示ZnT3可能在脑功能和生殖功能中具有重要作用。

关 键 词:  锌转运  ZnT3  cDNA  克隆  mRNA
文章编号:1000-8020(2002)02-0103-03
修稿时间:2001年4月28日

Cloning of ZnT3 cDNA and expression of ZnT3 mRNA in mice
Long Jiangang,Wang Fudi,Chen Jian,Shen Hui,et al..Cloning of ZnT3 cDNA and expression of ZnT3 mRNA in mice[J].Journal of Hygiene Research,2002,31(2):103-105.
Authors:Long Jiangang  Wang Fudi  Chen Jian  Shen Hui  
Affiliation:Department of Military Hygiene, Second Military Medical University, Shanghai 200433, China.
Abstract:In order to determine the level of mouse zinc transporter3 (ZnT3) mRNA expression, the fragment is cloned by RT-PCR method and is sequenced by dideoxynucleotide method. The expression of ZnT3 mRNA is also examined by RT-PCR method and is compared with beta-actin that served as the control. As the result, a proper single fragment of 700 bp is obtained with the sequence conformable to the corresponding fragment sequence of reported mouse ZnT3 cDNA. The ZnT3 mRNA is detected in cerebrum, hippocampus and in testis in that the highest expression is observed. However, the expression of ZnT3 mRNA is not detected in heart, liver, lung, spleen, kidney, intestine, olfactory bulb and cerebellum. The expression of ZnT3 mRNA in brain and testis suggests a physiologically functional importance of ZnT3 in mental and reproductive activities of mouse.
Keywords:zinc  zinc transport
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