Journal
DEVELOPMENTAL BIOLOGY
Volume 312, Issue 1, Pages 321-330Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2007.09.028
Keywords
egg activation; calcium; phospholipase C; RNAi; fertilization; mouse
Categories
Funding
- NICHD NIH HHS [R01 HD022732, HD22732, R01 HD022732-19, T32 HD007305] Funding Source: Medline
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Inositol 1,4,5-trisphosphate generated by the action of a phospholipase C (PLC) mediates release of intracellular Ca2+ that is essential for sperm-induced activation of mammalian eggs. Much attention currently focuses on the role of sperm-derived PLC in generating changes in egg intracellular Ca2+ despite the fact that PLC zeta constitutes a very small fraction of the total amount of PLC in a fertilized egg. Eggs express several isoforms of PLC, but a role for an egg-derived PLC in sperm-induced Ca2+ oscillations has not been examined. Reducing egg PLC beta 1 I by a transgenic RNAi approach resulted in a significant decrease in Ca2+ transient amplitude, but not duration or frequency, following insemination. Furthermore, overexpressing PLC beta 1 by microinjecting a Plc beta 1 cRNA significantly perturbed the duration and frequency of Ca2+ transients and disrupted the characteristic shape of the first transient. These results provide the first evidence for a role of an egg-derived PLC acting in conjunction with a sperm-derived PLC zeta in egg activation. (C) 2007 Elsevier Inc. All rights reserved.
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