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通过靶向同源重组将拷贝数控制元件整合到酵母人工染色体中。

Incorporation of copy-number control elements into yeast artificial chromosomes by targeted homologous recombination.

作者信息

Smith D R, Smyth A P, Strauss W M, Moir D T

机构信息

Collaborative Research, Inc., Waltham, Massachusetts 02154.

出版信息

Mamm Genome. 1993;4(3):141-7. doi: 10.1007/BF00352229.

Abstract

We have developed a pair of vectors for exchanging yeast artificial chromosome (YAC) arms by targeted homologous recombination. These conversion vectors allow the introduction of copy-number control elements into YACs constructed with pYAC4 or related vectors. YACs modified in this way provide an enriched source of DNA for genetic or biochemical studies. A LYS2 gene on the conversion vector provides a genetic selection for the modified YACs after transformation with appropriately prepared vector. A background of Lys+ clones that do not contain modified YACs is also present. However, clones with converted YACs can be distinguished from this background by counter-screening for loss of the original p YAC4 TRP1 arm (Trp- phenotype). The elimination of yeast replication origins (ARS elements) from the conversion vectors increased the frequency of Lys+ Trp- clones, but resulted in weaker amplification. Several YACs have been converted with these vectors, and the fate of the transformed DNA and of the resident YAC DNA has been systematically investigated.

摘要

我们开发了一对用于通过靶向同源重组交换酵母人工染色体(YAC)臂的载体。这些转化载体允许将拷贝数控制元件引入用pYAC4或相关载体构建的YAC中。以这种方式修饰的YAC为遗传或生化研究提供了丰富的DNA来源。转化载体上的LYS2基因在用适当制备的载体转化后为修饰的YAC提供遗传选择。也存在不含修饰YAC的Lys +克隆背景。然而,通过对原始pYAC4 TRP1臂的缺失进行反筛选(Trp-表型),可以将具有转化YAC的克隆与该背景区分开来。从转化载体中消除酵母复制起点(ARS元件)增加了Lys + Trp-克隆的频率,但导致扩增较弱。已经用这些载体转化了几个YAC,并且系统地研究了转化的DNA和常驻YAC DNA的命运。

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