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植入前对小鼠胚胎进行操作会导致发育第9.5天时印记基因的异常表达。

Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development.

作者信息

Rivera Rocío M, Stein Paula, Weaver Jamie R, Mager Jesse, Schultz Richard M, Bartolomei Marisa S

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Hum Mol Genet. 2008 Jan 1;17(1):1-14. doi: 10.1093/hmg/ddm280. Epub 2007 Sep 27.

Abstract

In vitro culture of mouse embryos results in loss of imprinting. The aim of the present study was to examine how two of the techniques commonly used during assisted reproduction, namely embryo culture and embryo transfer, affect genomic imprinting after implantation in the mouse. F1 hybrid mouse embryos were subjected to three experimental conditions: control (unmanipulated), embryo transfer and in-vitro-culture followed by embryo transfer. Concepti were collected on d9.5 of development and allelic expression determination of ten imprinted genes (H19, Snrpn, Igf2, Kcnq1ot1, Cdkn1c, Kcnq1, Mknr3, Ascl2, Zim1, Peg3) was performed. Although control concepti had monoallelic imprinted gene expression in all tissues, both manipulated groups had aberrant expression of one or more imprinted genes in the yolk sac and placenta. Culture further exacerbated the effects of transfer by increasing the number of genes with aberrant allelic expression in extraembryonic, as well as embryonic tissues. Additionally, placentae of both groups of manipulated concepti exhibited reduced levels of Igf2 mRNA and increased levels of Ascl2 mRNA when compared with their unmanipulated counterparts. Furthermore, we show that biallelic expression of Kcnq1ot1 coincided with loss of methylation on the maternal allele of the KvDMR1 locus, a phenotype often associated with the human syndrome Beckwith-Wiedemann. In conclusion, our results show that even the most basic manipulation used during human-assisted reproduction, namely, embryo transfer, can lead to misexpression of several imprinted genes during post-implantation development. Additionally, our results serve as a cautionary tale for gene expression studies in which embryo transfer is used.

摘要

小鼠胚胎的体外培养会导致印记丢失。本研究的目的是探讨辅助生殖过程中常用的两种技术,即胚胎培养和胚胎移植,如何影响小鼠植入后的基因组印记。F1杂种小鼠胚胎接受三种实验条件:对照(未处理)、胚胎移植以及体外培养后再进行胚胎移植。在发育的第9.5天收集胚胎,并对十个印记基因(H19、Snrpn、Igf2、Kcnq1ot1、Cdkn1c、Kcnq1、Mknr3、Ascl2、Zim1、Peg3)进行等位基因表达测定。虽然对照胚胎在所有组织中都有单等位基因印记基因表达,但两个处理组在卵黄囊和胎盘中都有一个或多个印记基因的异常表达。培养进一步加剧了移植的影响,增加了胚外组织以及胚胎组织中等位基因表达异常的基因数量。此外,与未处理的胚胎相比,两个处理组的胚胎胎盘均表现出Igf2 mRNA水平降低和Ascl2 mRNA水平升高。此外,我们发现Kcnq1ot1的双等位基因表达与KvDMR1位点母本等位基因甲基化的丧失相一致,这种表型通常与人类贝克威思-维德曼综合征相关。总之,我们的结果表明,即使是人类辅助生殖中最基本的操作,即胚胎移植,也会导致植入后发育过程中几个印记基因的错误表达。此外,我们的结果为使用胚胎移植的基因表达研究提供了警示。

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