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编号:11495370
结肠特异性基因RELMβ的克隆及其真核表达载体构建
http://www.100md.com 2007年7月28日 郑丽端, 童强松, 吕 清, 杨秀萍, 董继华
RELMβ基因;组织特异性;结肠;基因表达;免疫印迹;逆转录聚合酶链反应,郑丽端,杨秀萍,童强松,吕清,董继华,郑丽端,通讯作者:,Cloningofcolon-specificgeneresistin-likemoleculebetaan
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     郑丽端, 杨秀萍, 华中科技大学同济医学院附属协和医院病理科 湖北省武汉市 430022

    童强松, 吕清, 华中科技大学同济医学院附属协和医院外科 湖北省武汉市 430022

    董继华, 华中科技大学同济医学院附属协和医院中心实验室 湖北省武汉市 430022

    郑丽端, 医学博士, 主治医师, 主要从事消化系统疾病的分子病理研究.

    国家自然科学基金资助项目, No. 30600278

    通讯作者: 童强松, 430022, 湖北省武汉市, 华中科技大学同济医学院附属协和医院外科. qs_tong@hotmail.com

    电话: 027-85726129

    收稿日期: 2007-03-18 修回日期: 2007-07-24

    Cloning of colon-specific gene resistin-like molecule beta and construction of its eukaryotic expression vector

    
Li-Duan Zheng, Qiang-Song Tong, Qing Lv, Xiu-Ping Yang, Ji-Hua Dong

    Li-Duan Zheng, Xiu-Ping Yang,
Department of Pathology, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China

    Qiang-Song Tong, Qing Lv, Department of Surgery, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China

    Ji-Hua Dong, Department of Central Laboratory, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China

    Supported by: National Natural Science Foundation of China, No. 30600278

    Correspondence to: Dr. Qiang-Song Tong, Department of Surgery, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China. qs_tong@hotmail.com

    Received: 2007-03-18 Revised: 2007-07-24

    Abstract

    AIM: To clone mouse resistin-like molecule beta (RELMβ), a colon-specific gene, and construct its eukaryotic expression vector.

    METHODS: RELMβ expression in diverse organs and tissues in mice was investigated by Western and Northern blotting. Total RNA was extracted from mouse colon tissues. Full-length cDNA of the RELMβ gene was amplified by reverse transcriptase-polymerase chain reaction (RT-PCR), inserted into T/A vector, validated by nucleic acid sequencing, and subcloned into the EcoRI restriction site of eukaryotic vector pcDNA3 ......

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