首页> 美国卫生研究院文献>Molecular and Cellular Biology >Structural alterations of the aprt locus induced by deoxyribonucleoside triphosphate pool imbalances in Chinese hamster ovary cells.
【2h】

Structural alterations of the aprt locus induced by deoxyribonucleoside triphosphate pool imbalances in Chinese hamster ovary cells.

机译:在中国仓鼠卵巢细胞中由脱氧核糖核苷三磷酸池不平衡诱导的apt位点的结构改变。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Mutants induced at the adenine phosphoribosyl transferase (aprt) locus by dTTP or dCTP pool imbalances were examined for alterations in genomic DNA sequences. No observable changes were detected by Southern blot analysis of most mutant DNAs, suggesting induction of base pair alterations or other events below our level of detection (approximately 30 base pairs). However, in a few strains (11 from a total collection of 125 mutant cell strains), we were able to localize these events to restriction endonuclease recognition sequences when the mutations resulted in the loss or gain of a particular site. The distribution of lost or gained sites in aprt-deficient mutants induced by the two types of pool imbalances clearly varied, with those occurring in a mutator strain with increased dCTP clustering at one end of the aprt gene. Mutants induced by dTTP also revealed novel events: multiple restriction site modifications in a small region of the aprt gene in one mutant and a small (approximately 50 base pairs) insertion or duplication of DNA sequences. As in previous studies, very few deletion or insertion mutants were detected at the aprt locus. The significance of these findings in terms of the known biochemical and genetic consequences of these pool imbalances is discussed.
机译:检查了由dTTP或dCTP库不平衡在腺嘌呤磷酸核糖转移酶(aprt)位点诱导的突变体的基因组DNA序列变化。大多数突变体DNA的Southern印迹分析均未检测到可观察到的变化,这表明在我们检测水平以下(约30个碱基对)诱导了碱基对改变或其他事件。但是,在少数菌株中(总共125个突变细胞株中有11个),当突变导致特定位点的丢失或获得时,我们能够将这些事件定位在限制性核酸内切酶识别序列上。由两种类型的池不平衡引起的aprt缺失突变体中丢失或获得的位点的分布明显变化,那些发生在突变株中且dCTP簇在aprt基因的一端增加。 dTTP诱导的突变体也揭示了新的事件:一个突变体中aprt基因的小区域有多个限制性位点修饰,DNA序列的插入(或插入)很小(约50个碱基对)。与以前的研究一样,在aprt位点几乎没有检测到缺失或插入突变。讨论了这些发现对这些池失衡的已知生化和遗传后果的意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号