Cell cycle-dependent Ca2+ oscillations in mouse embryos are regulated by nuclear targeting of PLCζ

被引:111
|
作者
Larman, MG
Saunders, CM
Carroll, J
Lai, FA
Swann, K
机构
[1] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[2] Cardiff Univ, Coll Med, Wales Heart Res Inst, Cell Signalling Lab, Cardiff CF14 4XN, S Glam, Wales
[3] UCL, Dept Physiol, London WC1E 6BT, England
关键词
fertilisation; phospholipase C; Ca2+ oscillations; cell cycle;
D O I
10.1242/jcs.01109
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During the first cell cycle Ca2+ oscillations are regulated in a cell cycle-dependent manner, such that the oscillations are unique to M phase. How the Ca2+ oscillations are regulated with such cell cycle stage-dependency is unknown, despite their importance for egg activation and embryo development. We recently identified a novel, sperm-specific phospholipase C (PLCzeta; PLCzeta) that triggers Ca2+ oscillations similar to those caused by sperm. We show that PLCzeta-induced Ca2+ oscillations also occur exclusively during M phase. The cell cycle-dependency can be explained by PLCzeta's localisation to the pronuclei, which depends specifically upon a nuclear localisation signal sequence. Preventing pronuclear localisation. of PLC by mutation of the nuclear localisation signal, or by inhibiting pronuclear formation/import, can prolong Ca2+ oscillations or allow them to occur during interphase. These data suggest a novel mechanism for regulating a PLC through nuclear sequestration and may explain the cell cycle-dependent regulation of Ca2+ oscillations following fertilisation.
引用
收藏
页码:2513 / 2521
页数:9
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