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Abstract
Epigenetic perturbations are assumed to be responsible for
abnormalities observed in fetuses and offspring derived by
in vitro techniques. We have designed an experiment with
bovine day 80 fetuses generated by somatic cell nuclear
transfer (SCNT), in vitro fertilization (IVF), and
artificial insemination (AI) to determine the relationship
between fetal phenotype and genome-wide 5-methylcytosine
(5mC) content. When compared with AI controls, SCNT and
IVF fetuses displayed significantly increased body weight
(61%/28%), liver weight (100%/36%) and thorax
circumference (20%/11%). A reduced crown rump length :
thorax circumference ratio (1.175±0.017 in SCNT
and 1.292±0.018 in IVF vs. 1.390±0.018 in
AI, P<0.001 and P<0.002) was the external hallmark of this
disproportionate overgrowth phenotype. The SCNT fetuses
showed significant hypermethylation of liver DNA in
comparison with AI controls (3.46±0.08% vs.
3.17±0.09% 5mC, P<0.03), and the cytosine
methylation levels for IVF fetuses (3.34±0.09%)
were, as observed for phenotypic parameters, intermediate
to the other groups. Regressions of fetal body and liver
weight, and thorax circumference on 5mC-content of liver
DNA were positive (P<0.073-0.079). Furthermore, a
significant negative regression (P<0.021) of the crown
rump length : thorax circumference ratio on liver 5mC was
observed. The 5mC-content of placental cotyledon DNA was
46% lower than in liver DNA (P<0.001), but did not differ
among groups. These data are in striking contrast to the
recently reported hypomethylation of DNA from SCNT fetuses
and indicate that hypermethylation of fetal tissue, but
not placenta, is linked to the overgrowth phenotype in
bovine SCNT and IVF fetuses.
Key words:
Embryo
Assisted Reproductive Technology
Conceptus
Developmental biology
Placenta
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