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In vitro culture and somatic cell nuclear transfer affect imprinting of SNRPN gene in pre- and post-implantation stages of development in cattle

Authors :
Joao Suzuki
Jacinthe Therrien
France Filion
Rejean Lefebvre
Alan K Goff
Lawrence C Smith
Source :
BMC Developmental Biology, Vol 9, Iss 1, p 9 (2009), BMC Developmental Biology
Publisher :
Springer Nature

Abstract

Background Embryo in vitro manipulations during early development are thought to increase mortality by altering the epigenetic regulation of some imprinted genes. Using a bovine interspecies model with a single nucleotide polymorphism, we assessed the imprinting status of the small nuclear ribonucleoprotein polypeptide N (SNRPN) gene in bovine embryos produced by artificial insemination (AI), in vitro culture (IVF) and somatic cell nuclear transfer (SCNT) and correlated allelic expression with the DNA methylation patterns of a differentially methylated region (DMR) located on the SNRPN promoter. Results In the AI group, SNRPN maternal expression is silenced at day 17 and 40 of development and a third of the alleles analyzed are methylated in the DMR. In the IVF group, maternal transcripts were identified at day 17 but methylation levels were similar to the AI group. However, day-40 fetuses in the IVF group showed significantly less methylation when compared to the AI group and SNRPN expression was mostly paternal in all fetal tissues studied, except in placenta. Finally, the SCNT group presented severe loss of DMR methylation in both day-17 embryos and 40 fetuses and biallelic expression was observed in all stages and tissues analyzed. Conclusion Together these results suggest that artificial reproductive techniques, such as prolonged in vitro culture and SCNT, lead to abnormal reprogramming of imprinting of SNRPN gene by altering methylation levels at this locus.

Details

Language :
English
ISSN :
1471213X
Volume :
9
Issue :
1
Database :
OpenAIRE
Journal :
BMC Developmental Biology
Accession number :
edsair.doi.dedup.....25111896588b0b55cad7c508d7a894cf
Full Text :
https://doi.org/10.1186/1471-213x-9-9