Loveall Brandon J, Deitcher David L
Department of Neurobiology and Behavior, Cornell University, Ithaca, NY 14853, USA.
BMC Dev Biol. 2010 Aug 31;10:92. doi: 10.1186/1471-213X-10-92.
The protective external cuticle of insects does not accommodate growth during development. To compensate for this, the insect life cycle is punctuated by a series of molts. During the molt, a new and larger cuticle is produced underneath the old cuticle. Replacement of the smaller, old cuticle culminates with ecdysis, a stereotyped sequence of shedding behaviors. Following each ecdysis, the new cuticle must expand and harden. Studies from a variety of insect species indicate that this cuticle hardening is regulated by the neuropeptide bursicon. However, genetic evidence from Drosophila melanogaster only supports such a role for bursicon after the final ecdysis, when the adult fly emerges. The research presented here investigates the role that bursicon has at stages of Drosophila development which precede adult ecdysis.
We addressed the mechanism and timing of hormonal release from bursicon-positive motor neurons at the larval neuromuscular junction. Our findings indicate that vesicle membrane proteins which are required for classical neurotransmitter release are also expressed at these peptidergic motor neuron terminals; and that these terminals secrete hormones including bursicon at the neuromuscular junction, coinciding with larval ecdysis. This release surprisingly occurs in two waves, indicating bursicon secretion preceding and following the ecdysis sequence. Next, we addressed the functional significance of bursicon signaling during development, by disrupting the expression of its receptor, rickets, in different target tissues. We determined that rickets is developmentally required in the epidermis and imaginal discs for proper formation of the prepupa. It is also required to harden the pharate adult cuticle before eclosion. Significantly, we have also found that the available rickets mutants are not genetic nulls as previously believed, which necessitated the use of targeted RNA interference to disrupt rickets expression.
Our results are consistent with the view that bursicon is the insect tanning hormone. However, this is the first study to rigorously demonstrate both its release and function during development. Importantly, we provide new evidence that bursicon release can precede the initiation of larval ecdysis, and that bursicon tans the puparium. Our results firmly establish bursicon signaling as essential to insect growth and development.
昆虫的保护性外皮在发育过程中无法适应生长。为了弥补这一点,昆虫的生命周期被一系列蜕皮所打断。在蜕皮期间,旧外皮下方会产生一层新的、更大的外皮。较小的旧外皮的替换以蜕皮结束,这是一系列固定的蜕皮行为。每次蜕皮后,新外皮必须扩展并硬化。来自多种昆虫物种的研究表明,这种外皮硬化受神经肽bursicon调节。然而,黑腹果蝇的遗传学证据仅支持bursicon在最终蜕皮后(即成年果蝇出现时)发挥这样的作用。此处呈现的研究调查了bursicon在果蝇成年蜕皮之前的发育阶段所起的作用。
我们研究了幼虫神经肌肉接头处bursicon阳性运动神经元激素释放的机制和时间。我们的发现表明,经典神经递质释放所需的囊泡膜蛋白也在这些肽能运动神经元末端表达;并且这些末端在神经肌肉接头处分泌包括bursicon在内的激素,与幼虫蜕皮同时发生。这种释放令人惊讶地分两波进行,表明bursicon在蜕皮序列之前和之后都有分泌。接下来,我们通过破坏其受体rickets在不同靶组织中的表达,研究了bursicon信号在发育过程中的功能意义。我们确定,rickets在表皮和成虫盘发育过程中对于预蛹的正常形成是必需的。它在羽化前使准成虫外皮硬化也是必需的。重要的是,我们还发现现有的rickets突变体并非如先前认为的那样是基因无效突变体,这使得有必要使用靶向RNA干扰来破坏rickets的表达。
我们的结果与bursicon是昆虫鞣化激素这一观点一致。然而,这是第一项严格证明其在发育过程中的释放和功能的研究。重要的是,我们提供了新的证据表明bursicon释放可以在幼虫蜕皮开始之前发生,并且bursicon能鞣化蛹壳。我们的结果牢固地确立了bursicon信号对于昆虫生长和发育至关重要。