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一个有助于在酵母中对克隆基因进行转座子和插入诱变的载体家族。

A family of vectors that facilitate transposon and insertional mutagenesis of cloned genes in yeast.

作者信息

Allen J B, Elledge S J

机构信息

Verna & Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, TX 77030.

出版信息

Yeast. 1994 Oct;10(10):1267-72. doi: 10.1002/yea.320101003.

Abstract

This report describes two sets of plasmid vectors that facilitate the identification of regions of complementation in cloned genomic inserts via transposon or insertional mutagenesis. The first set contains ARS-H4 CEN6, a yeast selectable nutritional marker (HIS3, TRP1 or URA3), and neo for selection in Escherichia coli. These plasmids lack the Tn3 transposition immunity region present in pBR322 derived vectors, and are permissive recipients for Tn3 transposon mutagenesis. The second family of plasmids described facilitate gene disruption procedures performed in vitro. These vectors carry disruption cassettes that contain different yeast selectable markers (HIS3, LEU2, TRP1 or URA3) adjacent to the Tn5 neo gene. These genes can be excised as a cassette on a common restriction fragment and introduced into any desired restriction site with selection for kanamycin resistance.

摘要

本报告描述了两组质粒载体,它们可通过转座子或插入诱变来促进对克隆基因组插入片段中互补区域的鉴定。第一组包含ARS-H4 CEN6、一个酵母可选择营养标记(HIS3、TRP1或URA3)以及用于在大肠杆菌中进行选择的neo。这些质粒缺乏pBR322衍生载体中存在的Tn3转座免疫区域,是Tn3转座子诱变的允许受体。所描述的第二组质粒有助于体外进行的基因破坏程序。这些载体携带破坏盒,其中包含与Tn5 neo基因相邻的不同酵母可选择标记(HIS3、LEU2、TRP1或URA3)。这些基因可以作为一个盒在一个共同的限制片段上切除,并引入到任何所需的限制位点,同时选择卡那霉素抗性。

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