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

• 技术与方法 • Previous Articles     Next Articles

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

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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