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PMID: 17901045 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

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

Human molecular genetics ·Vol. 17 ·No. 1 ·2008-01-01 ·Pages 1-14

Rivera RM, Stein P, Weaver JR, Mager J, Schultz RM, Bartolomei MS

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.

MeSH Terms
Alleles Animals Basic Helix-Loop-Helix Transcription Factors/genetics Cyclin-Dependent Kinase Inhibitor p57/genetics DNA Methylation Embryo Culture Techniques Embryo Transfer/adverse effects Embryonic Development/genetics Female Gene Expression Regulation, Developmental Genomic Imprinting Gestational Age Humans Insulin-Like Growth Factor II/genetics Male Mice Mice, Inbred C57BL Mice, Transgenic Placenta/embryology,metabolism Pregnancy RNA, Long Noncoding RNA, Messenger/genetics,metabolism RNA, Untranslated/genetics Reproductive Techniques, Assisted/adverse effects Yolk Sac/embryology,metabolism
Chemicals
Ascl2 protein, mouse Basic Helix-Loop-Helix Transcription Factors Cdkn1c protein, mouse Cyclin-Dependent Kinase Inhibitor p57 H19 long non-coding RNA IGF2 protein, mouse RNA, Long Noncoding RNA, Messenger RNA, Untranslated Insulin-Like Growth Factor II
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Rivera Rocío M
Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Stein Paula
Weaver Jamie R
Mager Jesse
Schultz Richard M
Bartolomei Marisa S
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
2008-01-01
Epub
2007-00-27
Pages
1-14
Language
English
Region
England
NLM ID
9208958
Subset
IM
Grants
NIGMS NIH HHS · 5 T32 GM07229-33 · United States
NICHD NIH HHS · HD42026 · United States
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