| 著者 |
Tsukamoto T, Kwah JK, Zweifel ME, Courtemanche N, Gearhart MD, Walstrom KM, Jaramillo-Lambert A, Greenstein D.
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| Abstract |
Fertilization triggers the completion of female meiosis and launches the oocyte-to-embryo transition. Caenorhabditis elegans spe-11 is one of the few known paternal-effect embryonic lethal genes. We report that the sperm protein SPE-11 forms a complex with an oocyte protein, OOPS-1 (Oocyte Partner of SPE-11) at fertilization, and that the protein complex is required for the completion of meiosis, the block to polyspermy, and eggshell formation. Consistent with the molecular interaction of their encoded proteins, oops-1 and spe-11 exhibit indistinguishable null phenotypes in which fertilized oocytes arrest in meiosis I or meiosis II or fail to complete the actin-based process of meiotic cytokinesis. Biochemical analysis shows that the complex binds F-actin in the absence of other proteins and inhibits the nucleation of actin filaments at substoichiometric concentrations. Both OOPS-1 and SPE-11 are intrinsically disordered proteins that are highly phosphorylated, and biochemical and genetic experiments define interactions with the sperm-specific protein phosphatase 1 homologs GSP-3/4. Genetic results suggest that the cortical EGG complex recruits the OOPS-1-SPE-11 complex at fertilization, which promotes meiotic cytokinesis and in turn activates synthesis of the eggshell.
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