These findings on gene expression in single embryonic stem cells are in concert with recent studies of early mammalian development, which reveal molecular heterogeneity and a stochasticity of gene expression
in blastomeres.
Not exact matches
More than half of the 91
blastomeres divided at least once, and 28 formed clumps that grew
in culture.
In Xenopus, Noggin can direct the progeny of early
blastomeres, not normally destined to contribute to the eyes, to a retinal fate [19], [20].
From our experience with Preimplantation Genetic Diagnosis (PGD) we saw that a low mutation load at the
blastomere stage reflects the mutation load
in the child when it is born.
This interpretation is supported by a previous study showing that the
blastomeres from arrested human embryos still divided
in vitro when isolated from the original embryos [42].
The results indicate the potential for individual
blastomere growth and development from parthenotes obtained from
in vitro maturation
in spite of the fact that we did not derive a pESC line at this time.
In our study, cleaved day 3 parthenotes were used to establish pESCs from single
blastomeres using derivation methods as previously described [41].
Only 18.8 % of
in vivo - derived embryos contained at least one
blastomere with chromosomal anomalies, compared to 69.2 % of OPU - IVF embryos (P < 0.01) and 84.6 % of IVM - IVF embryos (P < 0.001).
Likewise, the expression pattern of cdx - 2, a key transcription factor
in the trophoblast lineage, overlaps with that of Oct - 4, but within any
blastomere, cdx - 2 expression bears no consistent relationship to that of Oct - 4 or nanog until after the trophectoderm lineage has been sorted [9].
Subsequently, genome - wide haplotyping and copy - number profiling was applied to investigate the genomic architecture of 171 single bovine
blastomeres of 16
in vivo, 13 OPU - IVF and 13 IVM - IVF embryos.
Main results and the role of chance: The genomic stability of single
blastomeres in both of the
in vitro - cultured embryo cohorts was severely compromised (P < 0.0001), and the frequency of whole chromosome or segmental aberrations was higher
in embryos produced
in vitro than
in embryos derived
in vivo.