Department of Biology, Duke Center for Systems Biology, Duke University, Durham, North Carolina 27708-0338, USA.
Genetics. 2013 Jul;194(3):539-55. doi: 10.1534/genetics.113.150847.
It is widely appreciated that larvae of the nematode Caenorhabditis elegans arrest development by forming dauer larvae in response to multiple unfavorable environmental conditions. C. elegans larvae can also reversibly arrest development earlier, during the first larval stage (L1), in response to starvation. "L1 arrest" (also known as "L1 diapause") occurs without morphological modification but is accompanied by increased stress resistance. Caloric restriction and periodic fasting can extend adult lifespan, and developmental models are critical to understanding how the animal is buffered from fluctuations in nutrient availability, impacting lifespan. L1 arrest provides an opportunity to study nutritional control of development. Given its relevance to aging, diabetes, obesity and cancer, interest in L1 arrest is increasing, and signaling pathways and gene regulatory mechanisms controlling arrest and recovery have been characterized. Insulin-like signaling is a critical regulator, and it is modified by and acts through microRNAs. DAF-18/PTEN, AMP-activated kinase and fatty acid biosynthesis are also involved. The nervous system, epidermis, and intestine contribute systemically to regulation of arrest, but cell-autonomous signaling likely contributes to regulation in the germline. A relatively small number of genes affecting starvation survival during L1 arrest are known, and many of them also affect adult lifespan, reflecting a common genetic basis ripe for exploration. mRNA expression is well characterized during arrest, recovery, and normal L1 development, providing a metazoan model for nutritional control of gene expression. In particular, post-recruitment regulation of RNA polymerase II is under nutritional control, potentially contributing to a rapid and coordinated response to feeding. The phenomenology of L1 arrest will be reviewed, as well as regulation of developmental arrest and starvation survival by various signaling pathways and gene regulatory mechanisms.
人们普遍认为,线虫秀丽隐杆线虫的幼虫通过形成 dauer 幼虫来应对多种不利的环境条件来停止发育。线虫幼虫也可以在更早的第一幼虫阶段(L1)可逆地停止发育,以应对饥饿。“L1 停滞”(也称为“L1 休眠”)发生时没有形态改变,但伴随着抗应激能力的增强。热量限制和周期性禁食可以延长成虫寿命,而发育模型对于理解动物如何缓冲营养供应的波动、影响寿命至关重要。L1 停滞为研究营养对发育的控制提供了机会。鉴于其与衰老、糖尿病、肥胖症和癌症的相关性,人们对 L1 停滞的兴趣正在增加,并且已经确定了控制停滞和恢复的信号通路和基因调控机制。胰岛素样信号是一个关键的调节剂,它通过 microRNAs 进行修饰和作用。DAF-18/PTEN、AMP 激活的激酶和脂肪酸合成也参与其中。神经系统、表皮和肠道系统地参与了对停滞的调节,但细胞自主信号可能有助于生殖细胞的调节。已知有少数基因影响 L1 停滞期间的饥饿存活,其中许多基因也影响成虫寿命,反映了一个共同的遗传基础,值得进一步探索。在停滞、恢复和正常 L1 发育期间,mRNA 表达得到了很好的描述,为营养控制基因表达提供了一个后生动物模型。特别是,RNA 聚合酶 II 的募集后调节受到营养控制,可能有助于对喂养的快速和协调反应。将综述 L1 停滞的现象学,以及各种信号通路和基因调控机制对发育停滞和饥饿存活的调节。