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Gonadotropin stimulation contributes to an increased incidence of epimutations in ICSI-derived mice

机译:促性腺激素刺激导致ICSI衍生小鼠的表位突变发生率增加

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We previously demonstrated that intracytoplasmic sperm injection (ICSI), a type of assisted reproductive technology (ART), can induce epimutations and/or epimutant phenotypes in somatic tissues of adult mice produced by this method. In the present study, we compared the occurrence of epimutations in mice produced by natural conception, ICSI and somatic cell nuclear transfer. Surprisingly, we observed the highest frequency of epimutations in somatic tissues from ICSI-derived mice. We also observed a delay in reprogramming of the maternal allele of the imprinted H19 gene in spermatogonia from juvenile ICSI-derived male mice. These observations led us to hypothesize that the exposure of the maternal gametic genome to exogenous gonadotropins during the endocrine stimulation of folliculogenesis (superovulation) may contribute to the disruption of the normal epigenetic programming of imprinted loci in somatic tissues and/or epigenetic reprogramming in the germ line of ensuing offspring. To test this hypothesis, we uncoupled superovulation from ICSI by subjecting female mice to gonadotropin stimulation and then allowing them to produce offspring by natural mating. We found that mice produced in this way also exhibited epimutations and/or epimutant phenotypes in somatic tissues and delayed epigenetic reprogramming in spermatogenic cells, providing evidence that gonadotropin stimulation contributes to the induction of epimutations during ART procedures. Our results suggest that gonadotropin stimulation protocols used in conjunction with ART procedures should be optimized to minimize the occurrence of epimutations in offspring produced by these methods.
机译:我们以前证明胞浆内的精子注射(ICSI),一种辅助生殖技术(ART),可以在通过这种方法产生的成年小鼠的体细胞组织中诱导表观突变和/或表观突变表型。在本研究中,我们比较了自然受孕,ICSI和体细胞核移植产生的小鼠表位突变的发生率。出人意料的是,我们观察到了来自ICSI衍生小鼠的体细胞组织中最高频率的突变。我们还观察到从幼年ICSI衍生的雄性小鼠精原细胞中印迹H19基因的母亲等位基因的重编程延迟。这些观察结果使我们假设,在内分泌刺激卵泡生成(超排卵)过程中,母体配子基因组暴露于外源促性腺激素可能会破坏体组织中印迹基因座的正常表观遗传程序和/或细菌中的表观遗传重编程。随后的后代。为了验证这一假设,我们通过使雌性小鼠受到促性腺激素刺激,然后使其自然交配来产生后代,从而使超排卵与ICSI脱钩。我们发现以这种方式产生的小鼠在体细胞组织中还表现出表位变异和/或表位变异表型,并在生精细胞中延迟表观遗传重编程,从而提供了促性腺激素刺激在ART程序中诱导表位变异的证据。我们的结果表明,应将与ART程序结合使用的促性腺激素刺激方案进行优化,以最大程度地减少这些方法产生的后代中表位突变的发生。

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