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Premeiotic, post meiotic, pre mitotic, or postmitotic events are all possibilities if imprints are created during male and female gametogenesis. However, if only one of the daughter cells receives parental imprints following mitosis, this would result in two functionally different female gametes or two functionally different sperm cells.
The egg cell is generally asymmetric, having an animal pole (future ectoderm).It is covered with protective envelopes, with different layers. The first envelope – the one in contact with the membrane of the egg – is made of glycoproteins and is known as the vitelline membrane (zona pellucida in mammals).
For example, the gene encoding insulin-like growth factor 2 (IGF2/Igf2) is only expressed from the allele inherited from the male. Although imprinting accounts for a small proportion of mammalian genes, they play an important role in embryogenesis particularly in the formation of visceral structures and the nervous system.
Embedding of the blastocyst into the endometrium requires that it hatches from the zona pellucida, the egg coat that prevents adherence to the fallopian tube as the pre-embryo makes its way to the uterus. The use of blastocysts in in vitro fertilization (IVF) involves culturing a fertilized egg for five days before transferring it into the uterus.
The inner cell mass will give rise to the pre-embryo, [9] the amnion, yolk sac and allantois, while the fetal part of the placenta will form from the outer trophoblast layer. The embryo plus its membranes is called the conceptus , and by this stage the conceptus has reached the uterus .
Between the beginning of the G 1 phase (which is also after mitosis has occurred) and R, the cell is known as being in the G 1-pm subphase, or the post-mitotic phase. After R and before S, the cell is known as being in G 1-ps, or the pre S phase interval of the G 1 phase. [4]
Figure 1: Schematic of the cell cycle. outer ring: I = Interphase, M = Mitosis; inner ring: M = Mitosis, G 1 = Gap 1, G 2 = Gap 2, S = Synthesis; not in ring: G 0 = Gap 0/Resting. Replication timing refers to the order in which segments of DNA along the length of a chromosome are duplicated.
Though Wee1 is a fairly conserved negative regulator of mitotic entry, no general mechanism of cell size control in G2 has yet been elucidated. Biochemically, the end of G 2 phase occurs when a threshold level of active cyclin B1 / CDK1 complex, also known as Maturation promoting factor (MPF) has been reached. [ 4 ]