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

被引:12
作者
Kouprina, N [1 ]
Nikolaishvili, N [1 ]
Graves, J [1 ]
Koriabine, M [1 ]
Resnick, MA [1 ]
Larionov, V [1 ]
机构
[1] NIEHS, Mol Genet Lab, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1006/geno.1998.5727
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (C) 1999 Academic Press.
引用
收藏
页码:262 / 273
页数:12
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