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人类酵母人工染色体在重组缺陷型酵母菌株中增殖过程中的完整性

Integrity of human YACs during propagation in recombination-deficient yeast strains.

作者信息

Kouprina N, Nikolaishvili N, Graves J, Koriabine M, Resnick M A, Larionov V

机构信息

Laboratory of Molecular Genetics, NIEHS, Research Triangle Park, North Carolina, 27709, USA.

出版信息

Genomics. 1999 Mar 15;56(3):262-73. doi: 10.1006/geno.1998.5727.

Abstract

Several isogenic strains with defects in recombination/repair genes (RAD1, RAD50, RAD51, RAD52, RAD54, and RAD55) were examined for their ability to propagate accurately a variety of linear and circular yeast artificial chromosomes (YACs) containing human DNA inserts. To assess YAC stability, the human DNA inserts were internally marked by an ADE2-pBR-URA3 cassette. Following selection for Ura- clones on 5-fluoroorotic acid containing medium, the following types of YAC deletions were identified: (i) those caused by homologous recombination with a telomeric pBR sequence; (ii) internal deletions, presumed to occur by recombination between commonly occurring DNA repeats such as Alu and LINE sequences; and (iii) deletions leading to loss of part of a YAC arm. rad52 host strains, but not other recombination-deficient strains, decreased the rate of all types of YAC deletions 25- to 400-fold. We have also developed and tested kar1 strains with a conditional RAD52 gene that allow transfer of a YAC from any host into a recombination-deficient background. These strains provide an efficient tool for stabilization of YACs and are useful for allowing additional recombinational modification of YACs.

摘要

对几种在重组/修复基因(RAD1、RAD50、RAD51、RAD52、RAD54和RAD55)方面存在缺陷的同基因菌株,检测了它们准确增殖多种含有人类DNA插入片段的线性和环状酵母人工染色体(YAC)的能力。为评估YAC的稳定性,人类DNA插入片段通过ADE2-pBR-URA3盒进行内部标记。在含5-氟乳清酸的培养基上选择Ura-克隆后,鉴定出以下几种类型的YAC缺失:(i)由与端粒pBR序列的同源重组引起的缺失;(ii)内部缺失,推测是由常见DNA重复序列(如Alu和LINE序列)之间的重组导致的;(iii)导致YAC臂部分缺失的缺失。rad52宿主菌株而非其他重组缺陷菌株,使所有类型的YAC缺失率降低了25至400倍。我们还构建并测试了带有条件性RAD52基因的kar1菌株,该菌株可将YAC从任何宿主转移到重组缺陷背景中。这些菌株为稳定YAC提供了一种有效的工具,并且对于允许对YAC进行额外的重组修饰很有用。

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