Department of Biology, Texas A&M University, College Station, TX 77843-3258, USA.
Neuroscience. 2011 Feb 23;175:1-17. doi: 10.1016/j.neuroscience.2010.12.002. Epub 2010 Dec 9.
Prolonged nutrient limitation has been extensively studied due to its positive effects on life span. However, less is understood of how brief periods of starvation can have lasting consequences. In this study, we used genetics, biochemistry, pharmacology and behavioral analysis to show that after a limited period of starvation, the synthesis of egl-2-encoded ether-a-go-go (EAG) K+ channels and its C-terminal modifications by unc-43-encoded CaMKII have a perduring effect on C. elegans male sexual behavior. EGL-2 and UNC-43 interactions, induced after food deprivation, maintain reduced excitability in muscles involved in sex. In young adult males, spastic contractions occur in cholinergic-activated sex muscles that lack functional unc-103-encoded ERG-like K+ channels. Promoting EGL-2 and UNC-43 interactions in unc-103 mutant adult males by starving them for a few hours reduce spastic muscle contractions over multiple days. Although transient starvation during early adulthood has a hormetic effect of suppressing mutation-induced muscle contractions, the treatment reduces the ability of young wild-type (WT) males to compete with well-fed cohorts in siring progeny.
由于延长营养限制对寿命有积极影响,因此已经对其进行了广泛研究。但是,对于短暂的饥饿期如何产生持久的后果,人们的了解较少。在这项研究中,我们使用遗传学、生物化学、药理学和行为分析表明,在有限的饥饿期之后,由 unc-43 编码的 CaMKII 编码的 egl-2 编码的醚-a-go-go(EAG)K+通道及其 C 末端修饰对 C. elegans 雄性性行为具有持久的影响。饥饿后诱导的 EGL-2 和 UNC-43 相互作用可维持参与性行为的肌肉的兴奋性降低。在年轻的成年雄性中,在缺乏功能性 unc-103 编码的 ERG 样 K+通道的胆碱能激活的性肌肉中会发生痉挛性收缩。通过让 unc-103 突变体成年雄性饥饿几个小时来促进 EGL-2 和 UNC-43 的相互作用,可以减少痉挛性肌肉收缩,持续数天。尽管成年早期的短暂饥饿对抑制突变引起的肌肉收缩具有兴奋作用,但该治疗方法降低了年轻野生型(WT)雄性与饲养良好的群体竞争生育后代的能力。