Department of Zoology, National Museum of Natural Science, 1 Kuan-Chien Road, Taichung 404, Taiwan, ROC.
J Insect Physiol. 2011 Jul;57(7):978-85. doi: 10.1016/j.jinsphys.2011.04.014. Epub 2011 May 12.
Phosphorylation of the translational repressor 4E-binding protein (4E-BP) plays a critical role in regulating the overall translation levels in cells. In the present study, we investigated 4E-BP phosphorylation of Bombyx mori eggs by an immunoblot analysis of a conserved phospho-specific antibody to 4E-BP and demonstrated its role during embryonic development. When HCl treatment was applied to diapause-destined eggs at 20 h after oviposition, a dramatic increase in the phosphorylation of 4E-BP occurred 5 min after treatment with HCl, and high phosphorylation levels were maintained throughout embryonic stage in HCl-treated eggs compared to those in diapause (control) eggs. When HCl treatment was applied to diapause eggs on day 10 after oviposition, no dramatic activation in 4E-BP phosphorylation occurred, indicating stage-specific effects of HCl treatment. In both non-diapause eggs and eggs whose diapause had been terminated by chilling of diapausing eggs at 5°C for 70 days and then were transferred to 25°C, high phosphorylation levels of 4E-BP were also detected. Moreover, 4E-BP phosphorylation dramatically increased when dechorionated eggs were incubated in medium. The addition of rapamycin, a specific inhibitor of mammalian target of rapamycin (TOR) signaling, and LY294002, a phosphoinositide 3-kinase (PI3K) inhibitor, but not the mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) kinase (MEK) inhibitor, U0126, dose-dependently inhibited 4E-BP phosphorylation in dechorionated eggs, indicating that PI3K/TOR signaling is an upstream signaling event involved in 4E-BP phosphorylation. Examination of 4E-BP gene expression levels showed no differences between treatments with HCl and water in the first hour after treatment, indicating that changes in phosphorylation of 4E-BP upon HCl treatment are mainly regulated at the post-transcriptional level. In addition, MAPK pathways and glycogen synthase kinase (GSK)-3β phosphorylation were not significantly affected in the first hour after HCl treatment. These results demonstrate that the rapid phosphorylation of 4E-BP is an early signaling event in embryonic development in the eggs whose diapause initiation was prevented by HCl treatment, thus being involved in the embryonic development of B. mori.
磷酸化的翻译抑制剂 4E-结合蛋白(4E-BP)在调节细胞内的整体翻译水平中起着至关重要的作用。在本研究中,我们通过免疫印迹分析一种针对 4E-BP 的保守磷酸化特异性抗体,研究了家蚕卵的 4E-BP 磷酸化,并证明了其在胚胎发育过程中的作用。当在产卵后 20 小时用 HCl 处理滞育卵时,处理后 5 分钟,4E-BP 的磷酸化显著增加,与滞育(对照)卵相比,HCl 处理的卵在整个胚胎阶段保持高磷酸化水平。当在产卵后 10 天用 HCl 处理滞育卵时,4E-BP 磷酸化没有明显激活,表明 HCl 处理具有阶段特异性。在非滞育卵和通过将滞育卵在 5°C 下冷处理 70 天并转移到 25°C 来终止滞育的卵中,也检测到 4E-BP 的高磷酸化水平。此外,当脱壳卵在培养基中孵育时,4E-BP 磷酸化显著增加。雷帕霉素,一种哺乳动物雷帕霉素(mTOR)信号的特异性抑制剂,和 LY294002,一种磷酸肌醇 3-激酶(PI3K)抑制剂,但不是丝裂原活化蛋白激酶(MAPK)/细胞外信号调节激酶(ERK)激酶(MEK)抑制剂 U0126,剂量依赖性地抑制脱壳卵中的 4E-BP 磷酸化,表明 PI3K/mTOR 信号是涉及 4E-BP 磷酸化的上游信号事件。检查 4E-BP 基因表达水平表明,在处理后 1 小时内,HCl 和水之间的处理没有差异,表明 HCl 处理后 4E-BP 磷酸化的变化主要是在转录后水平上调节的。此外,在 HCl 处理后 1 小时内,MAPK 途径和糖原合酶激酶(GSK)-3β 磷酸化没有显著变化。这些结果表明,快速磷酸化的 4E-BP 是通过 HCl 处理阻止滞育起始的卵的胚胎发育中的早期信号事件,因此参与了家蚕的胚胎发育。