Egg activation
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After the fusion of the sperm plasma membrane and the egg plasma membrane after fertilization, animal eggs go through a process called egg activation to prepare the egg for development.
There are three functions of egg activation:
- Block to polyspermy
- Activation of egg metabolism
- Resumption of the cell cycle
Sperm trigger of egg activation
The sperm may trigger egg activation via the interaction between a sperm protein and an egg surface receptor. It is possible that a G protein receptor is activated by the sperm binding which activates a tyrosine kinase which then activates PLC. The inositol signaling system has been implicated as the pathway involved with egg activation. IP3 and DAG are produced from the cleavage of PIP2 by phospholipase C (PLC). However, another hypothesis is that a soluble 'sperm factor' diffuses from the sperm into the egg cytosol upon sperm-oocyte fusion. The results of this interaction could activate a signal transduction pathway that uses second messengers. A novel PLC isoform, PLC zeta, may be the equivalent of the mammalian sperm factor. A recent paper shows that mammaliam sperm contain PLC zeta which can start the signaling cascade[1]
Fast and Slow Block to Polyspermy
Polyspermy is the condition when multiple sperm fuse with a single egg. This results in duplications of genetic material. In sea urchins, the block to polyspermy comes from two mechanisms: the fast block and the slow block. The fast block is an electrical block to polyspermy. The resting potential of an egg is -70mV. After contact with sperm, an influx of sodium ions from the sea water increases the potential up to +20mV. The slow block is through a biochemical mechanism triggered by a wave of calcium increase. The rise of calcium is both necessary and sufficient to trigger the slow block. In the cortical reaction, cortical granules directly beneath the plasma membrane are released into the space between the plasma membrane and the vitelline membrane (the perivitelline space). An increase in calcium triggers this release. The contents of the granules contain proteases, mucopolysaccharides, hyalin, and peroxidases. The proteases cleave the bridges connecting the plasma membrane and the vitelline membrane and cleave the bindin to release the sperm. The mucopolysaccharides attract water to raise the vitelline membrane. The hyalin forms a layer adjacent to the plasma membrane and the peroxidases cross-link the protein in the vitelline membrane to harden it and make it impenetrable to sperm. Through these molecules the vitelline membrane is transformed into the fertilization membrane or fertilization envelope. In mice, the zona reaction is the equivalent to the cortical reaction in sea urchins. The terminal sugars from ZP3 are cleaved to release the sperm and prevent new binding.
Late Responses
The combined increase of calcium signal and pH leads to a dramatic increase in protein synthesis. The protein synthesis uses mRNAs that are already present in the oocyte. These proteins direct the next events of embryogenesis such as the fusion of the egg and sperm pronuclei to form the diploid embryonic nucleus. The fusion is driven by microtubule-dependent movement of the female pronucleus to the male pronucleus.
References
Stages of Development in Developmental Biology | |
|---|---|
| Early Embryonic Development | Fertilization - Egg activation - Cleavage - Gastrulation - Regional specification |
| Late Embryonic Development | Ectoderm: Neurulation - Neural crest - Eye development - Cutaneous structure development
Mesoderm: Heart development Other: Limb development - Germ line development - Programmed cell death - Stem cells |
| Post Embryonic Development | Metamorphosis - Regeneration - Aging |
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
