Identification of PLC gamma-dependent and -independent events during fertilization of sea urchin eggs

Citation
Dj. Carroll et al., Identification of PLC gamma-dependent and -independent events during fertilization of sea urchin eggs, DEVELOP BIO, 206(2), 1999, pp. 232-247
Citations number
82
Categorie Soggetti
Cell & Developmental Biology
Journal title
DEVELOPMENTAL BIOLOGY
ISSN journal
00121606 → ACNP
Volume
206
Issue
2
Year of publication
1999
Pages
232 - 247
Database
ISI
SICI code
0012-1606(19990215)206:2<232:IOPGA->2.0.ZU;2-X
Abstract
At fertilization, sea urchin eggs undergo a series of activation events, in cluding a Ca2+ action potential, Ca2+ release from the endoplasmic reticulu m, an increase in intracellular pH, sperm pronuclear formation, MAP liinase dephosphorylation, and DNA. synthesis. To examine which of these events mi ght be initiated by activation of phospholipase Cy (PLCgamma), which produc es the second messengers inositol trisphosphate (IP3) and diacylglycerol, w e used recombinant SH2 domains of PLC gamma as specific inhibitors. Sea urc hin eggs were co-injected with a GST fusion protein composed of the two tan dem SH2 domains of bovine PLC gamma and (1) Ca2+ green dextran to monitor i ntracellular free Ca2+, (2) BCECF dextran to monitor intracellular pH, (3) Oregon Green dUTP to monitor DNA synthesis, or (4) fluorescein 70-kDa dextr an to monitor nuclear envelope formation. Microinjection of the tandem SH2 domains of PLC gamma produced a concentration-dependent inhibition of Ca2release and also inhibited cortical granule exocytosis, cytoplasmic alkalin ization, MAP kinase dephosphorylation, DNA synthesis, and cleavage after fe rtilization. However, the Ca2+ action potential, sperm entry, and sperm pro nuclear formation were not prevented by injection of the PLC gamma SH2 doma in protein. Microinjection of a control protein, the tandem SH2 domains of the phosphatase SHP2, had no effect on Ca2+ release, cortical granule exocy tosis, DNA synthesis, or cleavage. Specificity of the inhibitory action of the PLC gamma SH2 domains was further indicated by the finding that microin jection of PLC gamma SH2 domains that had been point mutated at a critical arginine did not inhibit Ca release at fertilization. Additionally, Ca2+ re lease in response to microinjection of IF3, cholera toxin, cADP ribose, or cGMP was not inhibited by the PLC gamma SH2 fusion protein. These results i ndicate that PLC gamma plays a key role in several fertilization events in sea urchin eggs, including Ca2+ release and DNA synthesis, but that the act ion potential, sperm entry, and male pronuclear formation can occur in the absence of PLC gamma activation or Ca2+ increase. (C) 1999 Academic Press.