Abstract
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.
MeSH Terms
Alleles
Animals
Cornea/metabolism
Epithelium, Corneal/metabolism
Female
Gametogenesis/genetics
Gene Deletion
Gene Expression
Gene Expression Regulation, Enzymologic
Genes, Reporter
Integrases/genetics
Keratin-12/genetics,metabolism
Male
Mice
Mice, Inbred Strains
Mice, Transgenic
Recombination, Genetic
Spermatogenesis/genetics
Chemicals
Keratin-12
Cre recombinase
Integrases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Weng Daniel Y
Department of Ophthalmology, University of Cincinnati, Cincinnati, OH 45267-0838, USA.
Zhang Yujin
Hayashi Yasuhito
Kuan Chia-Yi
Liu Chia-Yang
Babcock George
Weng Wei-Lan
Schwemberger Sandy
Kao Winston W-Y
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