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本文引用的文献

1
Primary epimutations introduced during intracytoplasmic sperm injection (ICSI) are corrected by germline-specific epigenetic reprogramming.在细胞质内精子注射 (ICSI) 过程中引入的主要表观遗传突变通过种系特异性的表观遗传重编程得到纠正。
Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4163-8. doi: 10.1073/pnas.1201990109. Epub 2012 Feb 27.
2
The epigenome as a target for heritable environmental disruptions of cellular function.表观基因组作为细胞功能遗传性环境干扰的靶点。
Mol Cell Endocrinol. 2012 May 6;354(1-2):9-15. doi: 10.1016/j.mce.2011.09.014. Epub 2011 Sep 25.
3
Epigenetics and assisted reproductive technology.表观遗传学与辅助生殖技术。
J Intern Med. 2011 Nov;270(5):414-20. doi: 10.1111/j.1365-2796.2011.02445.x. Epub 2011 Sep 14.
4
Embryonic imprinting perturbations do not originate from superovulation-induced defects in DNA methylation acquisition.胚胎印迹干扰并非源于超排卵诱导的 DNA 甲基化获得缺陷。
Fertil Steril. 2011 Sep;96(3):734-738.e2. doi: 10.1016/j.fertnstert.2011.06.055. Epub 2011 Jul 22.
5
Side-by-side comparison of five commercial media systems in a mouse model: suboptimal in vitro culture interferes with imprint maintenance.在小鼠模型中对五种商业培养基的并排比较:体外培养条件不佳会干扰印迹维持。
Biol Reprod. 2010 Dec;83(6):938-50. doi: 10.1095/biolreprod.110.085480. Epub 2010 Aug 11.
6
Genomic imprinting in germ cells: imprints are under control.生殖细胞中的基因组印记:印记受调控。
Reproduction. 2010 Sep;140(3):411-23. doi: 10.1530/REP-10-0173. Epub 2010 May 25.
7
Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner.超排卵的双重效应:以剂量依赖的方式丢失母系和父系印迹甲基化。
Hum Mol Genet. 2010 Jan 1;19(1):36-51. doi: 10.1093/hmg/ddp465.
8
Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.通过辅助生殖技术受孕的临床正常儿童中,KvDMR1印记控制区域存在异常甲基化。
Mol Hum Reprod. 2009 Aug;15(8):471-7. doi: 10.1093/molehr/gap038. Epub 2009 Jun 3.
9
Implications of epigenetics and genomic imprinting in assisted reproductive technologies.表观遗传学和基因组印迹在辅助生殖技术中的意义。
Mol Reprod Dev. 2009 Nov;76(11):1006-18. doi: 10.1002/mrd.21058.
10
[Epimutations of imprinting genes in the human genome: classification, causes, association with hereditary pathology].[人类基因组中印迹基因的表观突变:分类、成因及与遗传性病理学的关联]
Genetika. 2008 Oct;44(10):1356-73.

促性腺激素刺激导致 ICSI 衍生小鼠中表观突变的发生率增加。

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

机构信息

Department of Biology, University of Texas, San Antonio, TX 78249, USA.

出版信息

Hum Mol Genet. 2012 Oct 15;21(20):4460-72. doi: 10.1093/hmg/dds287. Epub 2012 Jul 16.

DOI:10.1093/hmg/dds287
PMID:22802074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3459467/
Abstract

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.

摘要

我们之前的研究表明,卵细胞质内单精子注射(ICSI)作为一种辅助生殖技术(ART),可以在通过该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中表观突变的发生情况。令人惊讶的是,我们观察到 ICSI 衍生的小鼠体细胞组织中表观突变的频率最高。我们还观察到,在来自幼年 ICSI 衍生雄性小鼠的精原细胞中,印迹基因 H19 的母等位基因的重编程延迟。这些观察结果使我们假设,在卵泡发生的内分泌刺激(超排卵)过程中,母配子基因组暴露于外源性促性腺激素可能导致体细胞组织中印迹基因座的正常表观遗传编程和/或随后后代生殖细胞中的表观遗传重编程中断。为了验证这一假设,我们通过让雌性小鼠接受促性腺激素刺激,然后让它们通过自然交配来产生后代,从而使超排卵与 ICSI 脱耦。我们发现,以这种方式产生的小鼠在体细胞组织中也表现出表观突变和/或表观突变表型,并且在精原细胞中出现了延迟的表观遗传重编程,这为促性腺激素刺激在 ART 过程中诱导表观突变提供了证据。我们的结果表明,应优化与 ART 程序一起使用的促性腺激素刺激方案,以最大限度地减少这些方法产生的后代中表观突变的发生。