遗传 ›› 2006, Vol. 28 ›› Issue (9): 1123-1128.

• 技术与方法 • 上一篇    下一篇

应用PCR-酶切连接法合成全长sFat1基因

朱贵明1,2, 陈 宏1, 3, 卢建申2, 周艳荣2, 吴晓洁2, 陈红星2, 邓继先2   

  1. 1. 西北农林科技大学动物科技学院, 杨凌 712100; 2. 军事医学科学院生物工程研究所, 北京 100071; 3. 徐州师范大学细胞
    与分子生物学研究所, 徐州 221116

  • 收稿日期:2006-04-25 修回日期:2006-05-24 出版日期:2006-09-01 发布日期:2006-09-01
  • 通讯作者: 朱贵明

Synthesis of Total sFat-1 Gene by PCR-Restrict Enzyme Ligation Method

ZHU Gui-Ming1, 2, CHEN Hong1,3, LU Jian-Shen2, ZHOU Yan-Rong2, WU Xiao-Jie2,
CHEN Hong-Xing2, DENG Ji-Xian2
  

  1. College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China; 2. Institute of Biotechnology,
    Academy of Military Medical Sciences, Beijing 100071, China; 3. Institute of Cellular and Molecular Biology, Xuzhou Normal University, Xuzhou 221116, China
  • Received:2006-04-25 Revised:2006-05-24 Online:2006-09-01 Published:2006-09-01
  • Contact: ZHU Gui-Ming

摘要:

人工合成基因在生命科学研究中有着重要的意义, 因此基因合成是一项常用技术。长片段基因的合成比较困难, 常常因为合成中碱基序列的错配、突变等原因而导致失败。研究者们所熟知的几种现行的方法仍然难以解决该问题。本研究在作者自身的工作经验中建立了一种新的基因合成方法, 即PCR-酶切连接法。应用该方法成功地将化学合成的27个寡聚核苷酸片段(每个片段长60~68 bp)拼接组装起来, 获得了完整的总长为1 226 bp的基因sFat-1。整个过程仅采用3轮PCR(共7个反应)、2轮的酶切连接(3个反应), 而且未曾出现任何偏离预期基因序列的差错。该方法步骤较少, 技术简单, 出错极少, 是合成长基因序列很好的选择。

关键词: ω-3脂肪酸去饱和酶基因, 聚合酶链式反应, 基因合成

Abstract:

Gene synthesis is very important in life science research, and it becomes a technique in common use. It is difficult for long gene synthesis, because the mismatches and mutations of DNA sequence in nucleotide fragments assembling. This study established a new method for long gene synthesis, which was referred to as PCR-restrict enzyme ligation method. With this method, a ω-3 fatty acid desaturase gene, sFat-1, from Caenorhabditis briggssae, was successfully assembled from 27 synthesized nucleotide fragments(60~68 bp for each fragment ) following 3 rounds of PCR (7 reactions) and 2 rounds of restrict enzyme ligation (3 reactions). This shows that the PCR-restrict enzyme ligation method is an effective method for long gene synthesis.

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