Tamashiro Kellie L K, Wakayama Teruhiko, Akutsu Hidenori, Yamazaki Yukiko, Lachey Jennifer L, Wortman Matthew D, Seeley Randy J, D'Alessio David A, Woods Stephen C, Yanagimachi Ryuzo, Sakai Randall R
Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Nat Med. 2002 Mar;8(3):262-7. doi: 10.1038/nm0302-262.
Mammalian cloning using somatic cells has been accomplished successfully in several species, and its potential basic, clinical and therapeutic applications are being pursued on many fronts. Determining the long-term effects of cloning on offspring is crucial for consideration of future application of the technique. Although full-term development of animals cloned from adult somatic cells has been reported, problems in the resulting progeny indicate that the cloning procedure may not produce animals that are phenotypically identical to their cell donor. We used a mouse model to take advantage of its short generation time and lifespan. Here we report that the increased body weight of cloned B6C3F1 female mice reflects an increase of body fat in addition to a larger body size, and that these mice share many characteristics consistent with obesity. We also show that the obese phenotype is not transmitted to offspring generated by mating male and female cloned mice.
利用体细胞进行的哺乳动物克隆已在多个物种中成功实现,其潜在的基础、临床和治疗应用正在多个领域展开探索。确定克隆对后代的长期影响对于该技术未来的应用考量至关重要。尽管已有报道称从成年体细胞克隆的动物能够发育至足月,但所得后代出现的问题表明,克隆过程可能无法产生在表型上与其细胞供体完全相同的动物。我们利用小鼠模型,因其世代周期短和寿命较短。在此我们报告,克隆的B6C3F1雌性小鼠体重增加不仅反映出体型增大,还伴有体脂增加,并且这些小鼠具有许多与肥胖相符的特征。我们还表明,肥胖表型不会传递给克隆的雄性和雌性小鼠交配产生的后代。