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用于无PCR基因操作的基于化学反应的位点选择性DNA切割器。

Chemical-reaction-based site-selective DNA cutter for PCR-free gene manipulation.

作者信息

Yamamoto Yoji, Uehara Akihiko, Watanabe Akira, Aburatani Hiroyuki, Komiyama Makoto

机构信息

Research Center for Advanced Science and Technology, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, 153-8904, Japan.

出版信息

Chembiochem. 2006 Apr;7(4):673-7. doi: 10.1002/cbic.200500402.

Abstract

An artificial restriction DNA cutter (ARCUT), recently developed by the authors, was used to construct a fusion protein. The gene of WW-domain-containing oxidoreductase (WWOX) was cut by ARCUT just before its stop codon, and ligated to fuse the gene of enhanced green fluorescent protein (EGFP). The reading frames of two genes were adjusted to coincide each other. Throughout the manipulation, no PCR was employed. The fluorescent fusion protein was successfully expressed in mammalian cells, and showed entirely different subcellular localization from EGFP itself. Apparently, the DNA was kept completely intact during the manipulation. The man-made tool ARCUT has promising features for future biotechnology and molecular biology.

摘要

作者最近开发的一种人工限制性DNA切割器(ARCUT)被用于构建融合蛋白。含WW结构域的氧化还原酶(WWOX)基因在其终止密码子之前被ARCUT切割,并与增强型绿色荧光蛋白(EGFP)基因连接以融合。调整两个基因的阅读框使其相互一致。在整个操作过程中,未使用聚合酶链式反应(PCR)。荧光融合蛋白在哺乳动物细胞中成功表达,并且显示出与EGFP本身完全不同的亚细胞定位。显然,在操作过程中DNA保持完全完整。人造工具ARCUT在未来的生物技术和分子生物学方面具有广阔的应用前景。

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