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细胞因子人MK基因的克隆及在大肠杆菌中的高效表达(简报)
引用本文:黄建 林万敏 罗祖玉 谢毅. 细胞因子人MK基因的克隆及在大肠杆菌中的高效表达(简报)[J]. 分子细胞生物学报, 2001, 34(2): 143-146
作者姓名:黄建 林万敏 罗祖玉 谢毅
作者单位:黄建(复旦大学生理与生物物理学系,上海200433)      林万敏(复旦大学生理与生物物理学系,上海200433)      罗祖玉(复旦大学生理与生物物理学系,上海200433)      谢毅(复旦大学遗传学研究所遗传工程国家重点实验室,上海200433)
摘    要:细胞因子Midkine(简称MK)是新发现的一类肝素结合因子家族中的一员。1988年,Kadamatsu等利用差异杂交法在经维甲酸诱导分化的小鼠畸胎瘤细胞株HM-1中首先克隆到小鼠MK基因。人MK基因则最早是从λgt10人胚肾(20-24周)cDNA库和EMBL-3人胎盘基因组库获得。成熟

关 键 词:细胞因子人MK 克隆 原核表达
修稿时间:2000-08-02

CLONING AND EFFICIENT EXPRESSION OF CYTOKINE HUMAN MK IN E. coli
HUANG Jian LIN Wan Min LUO Zu Yu XIE Yi. CLONING AND EFFICIENT EXPRESSION OF CYTOKINE HUMAN MK IN E. coli[J]. Journal of Molecular Cell Biology, 2001, 34(2): 143-146
Authors:HUANG Jian LIN Wan Min LUO Zu Yu XIE Yi
Abstract:For cloning the cytokine human Midkine (MK) gene, we designed by PCgene program and synthesized a pair of PCR specific primers according to the reported human MK cDNA sequence. Total cellular RNA was extracted from a human hepatoblastoma cell line HepG2, and then the target DNA fragment was obtained by RT-PCR and subcloned into plasmid pUC118. Checked with radioisotope sequencing and ABI 377A sequencer, the nu-cleotide sequence of the cloned MK cDNA was identical with the reported one. A prokaryotic expression vector, named pBV220, was used to express the MK protein effi-ciently in E. coli strain TG1 and a predicted band of 16. 5 kD in Mr by 15% SDS-PAGE was found. The expressed recombinant protein was found in insoluble aggregated form and accounted for about 31.21% of the total cellular proteins. The first 15 N-terminal amino acid sequence analysis of this protein by Edman degradation method showed that it was accordant with that predicted from the cDNA sequence. The activity of neurite outgrowth-promoting of the MK crude samples was tested with brain cells isolated from 18-day embryos of SD rat.
Keywords:Cytokine human midkine (MK). Cloning. Prokaryotic expression.  
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