Weng Daniel Y, Zhang Yujin, Hayashi Yasuhito, Kuan Chia-Yi, Liu Chia-Yang, Babcock George, Weng Wei-Lan, Schwemberger Sandy, Kao Winston W-Y
Department of Ophthalmology, University of Cincinnati, Cincinnati, OH 45267-0838, USA.
Mol Vis. 2008 Mar 20;14:562-71.
To examine whether promiscuous Cre/LoxP recombination happens during gametogenesis in double transgenic mice carrying LoxP modified alleles and Cre transgene driven by tissue-specific promoter outside the gonads of adult mice.
Cre driver mice were crossbred with reporter mouse lines (e.g., ZEG and Rosa26R) to obtain Cre/ZEG and Cre/Rosa26R double transgenic mice. The frequency of promiscuous LoxP/Cre recombination was determined by the expression of second reporter genes in the offspring of double transgenic mice.
The frequency of promiscuous LoxP/Cre recombination varied in different lines of Cre driver mice and in the sex of the same driver mice with higher penetrance in male than in female double transgenic mice. Polymerase chain reaction (PCR) and recombination analysis demonstrate that the recombination of floxed allele occurs during the transition from spermatogonia (diploid) to primary spermatocyte (tetraploid) in the testis. Thereby, target-floxed allele(s) may be ubiquitously ablated in experimental animals intended for tissue-specific gene deletion.
Gametogenesis-associated recombination should always be examined in tissue-specific gene ablation studies.
研究在成年小鼠性腺外携带LoxP修饰等位基因和由组织特异性启动子驱动的Cre转基因的双转基因小鼠配子发生过程中,是否会发生杂乱的Cre/LoxP重组。
将Cre驱动小鼠与报告基因小鼠品系(如ZEG和Rosa26R)杂交,以获得Cre/ZEG和Cre/Rosa26R双转基因小鼠。通过双转基因小鼠后代中第二个报告基因的表达来确定杂乱的LoxP/Cre重组频率。
杂乱的LoxP/Cre重组频率在不同品系的Cre驱动小鼠以及同一驱动小鼠的不同性别中有所不同,在雄性双转基因小鼠中的穿透率高于雌性。聚合酶链反应(PCR)和重组分析表明,在睾丸中,floxed等位基因的重组发生在精原细胞(二倍体)向初级精母细胞(四倍体)转变的过程中。因此,在旨在进行组织特异性基因缺失的实验动物中,目标floxed等位基因可能会被普遍消除。
在组织特异性基因敲除研究中,应始终检测与配子发生相关的重组。