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. 2020 Dec 28;22(1):236. doi: 10.3390/ijms22010236

Table 1.

Epigenetic barriers to somatic cell nuclear transfer cloning.

Epigenetic Barrier Where Reference
Memory of an active transcriptional state Donor cells [55,56]
Imprinting disorder in donor cells Fibroblasts from abnormal cloned fetuses [57]
Misregulation of mRNAs at the time of ZGA Early stage NT embryos [35]
Disturbed transcription by RNA polymerase I around ZGA Early stage NT embryos [38]
Non-proper degradation of maternally stored transcripts Early stage NT embryos [35]
Continuous expression of some somatic genes around ZGA Early stage NT embryos [40]
Resistance to reprogramming of pluripotency genes Early to blastocyst stage
NT embryos
[41,42]
Defective epigenetic reprogramming of DNA and histones NT embryos [27,46,58]
Abnormal regulation of DNA methyltransferase expression NT embryos [59]
Incomplete erasure of the somatic type of DNA methylation and somatic cell-like features NT embryos [40,51,60]
Failure to reactivate X chromosome and aberrant X chromosome inactivation (XCI) NT embryos [61,62]
Aberrant remethylation leading to mis-expression of genes and retrotransposons important for ZGA NT embryos [63]
Disruption of imprinted gene methylation and expression NT embryos [64,65]
Loss of imprinting NT embryos [53]
Defective trophoblast cell lineage specification NT blastocysts [66,67]
Abnormal gene expression profiles in cloned placenta Extra-embryonic tissues [68,69,70]
Abnormal imprinted gene expression and methylation patterns in mid-gestation Cloned fetuses and placentas [57,71,72,73,74,75,76]