An extra maternally derived X chromosome (X M ) but not a paternally derived one (X P ) is detrimental in early mouse embryogenesis resulting in failure to form the ectoplacental cone and extra‐embryonic ectoderm. Cytogenetic studies suggested that two X M chromosomes remain active in the trophectoderm and possibly also the primitive endoderm, in which X P is preferentially inactivated in normal female embyos. Two copies of an active X chromosome due to maternal imprinting seem to prevent further differentiation of the trophectoderm.
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Nobuo Takagi (1991) studied this question.
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