Yamagishi Yuka, Abe Hiroshi
Department of Nanobiology, Graduate School of Advanced Integration Science, Chiba University, Chiba 263-8522, Japan.
Department of Nanobiology, Graduate School of Advanced Integration Science, Chiba University, Chiba 263-8522, Japan
Mol Biol Cell. 2015 Dec 1;26(24):4387-400. doi: 10.1091/mbc.E15-01-0035. Epub 2015 Sep 30.
We examined the reorganization of actin filaments and microtubules during Xenopus oocyte maturation. Surrounding the germinal vesicle (GV) in immature oocytes, the cytoplasmic actin filaments reorganized to accumulate beneath the vegetal side of the GV, where the microtubule-organizing center and transient microtubule array (MTOC-TMA) assembled, just before GV breakdown (GVBD). Immediately after GVBD, both Xenopus ADF/cofilin (XAC) and its phosphatase Slingshot (XSSH) accumulated into the nuclei and intranuclear actin filaments disassembled from the vegetal side with the shrinkage of the GV. As the MTOC-TMA developed well, cytoplasmic actin filaments were retained at the MTOC-TMA base region. Suppression of XAC dephosphorylation by anti-XSSH antibody injection inhibited both actin filament reorganization and proper formation and localization of both the MTOC-TMA and meiotic spindles. Stabilization of actin filaments by phalloidin also inhibited formation of the MTOC-TMA and disassembly of intranuclear actin filaments without affecting nuclear shrinkage. Nocodazole also caused the MTOC-TMA and the cytoplasmic actin filaments at its base region to disappear, which further impeded disassembly of intranuclear actin filaments from the vegetal side. XAC appears to reorganize cytoplasmic actin filaments required for precise assembly of the MTOC and, together with the MTOC-TMA, regulate the intranuclear actin filament disassembly essential for meiotic spindle formation.
我们研究了非洲爪蟾卵母细胞成熟过程中肌动蛋白丝和微管的重组。在未成熟卵母细胞中,围绕生发泡(GV)的细胞质肌动蛋白丝发生重组,在生发泡破裂(GVBD)前,聚集在GV植物极一侧下方,微管组织中心和瞬时微管阵列(MTOC-TMA)在此处组装。GVBD后立即,非洲爪蟾ADF/丝切蛋白(XAC)及其磷酸酶弹弓蛋白(XSSH)都积累到细胞核中,随着GV收缩,核内肌动蛋白丝从植物极一侧解体。随着MTOC-TMA充分发育,细胞质肌动蛋白丝保留在MTOC-TMA基部区域。通过注射抗XSSH抗体抑制XAC去磷酸化,会抑制肌动蛋白丝重组以及MTOC-TMA和减数分裂纺锤体的正确形成和定位。用鬼笔环肽稳定肌动蛋白丝也会抑制MTOC-TMA的形成和核内肌动蛋白丝的解体,而不影响核收缩。诺考达唑也会导致MTOC-TMA及其基部区域的细胞质肌动蛋白丝消失,这进一步阻碍了核内肌动蛋白丝从植物极一侧的解体。XAC似乎会重组MTOC精确组装所需的细胞质肌动蛋白丝,并与MTOC-TMA一起调节减数分裂纺锤体形成所必需的核内肌动蛋白丝解体。