Neural mechanism of circadian clock-based photoperiodism in insects and snails.

IF 1.9 4区 心理学 Q3 BEHAVIORAL SCIENCES Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology Pub Date : 2024-07-01 Epub Date: 2023-08-18 DOI:10.1007/s00359-023-01662-6
Yoshitaka Hamanaka, Masaharu Hasebe, Sakiko Shiga
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Abstract

The photoperiodic mechanism distinguishes between long and short days, and the circadian clock system is involved in this process. Although the necessity of circadian clock genes for photoperiodic responses has been demonstrated in many species, how the clock system contributes to photoperiodic mechanisms remains unclear. A comprehensive study, including the functional analysis of relevant genes and physiology of their expressing cells, is necessary to understand the molecular and cellular mechanisms. Since Drosophila melanogaster exhibits a shallow photoperiodism, photoperiodic mechanisms have been studied in non-model species, starting with brain microsurgery and neuroanatomy, followed by genetic manipulation in some insects. Here, we review and discuss the involvement of the circadian clock in photoperiodic mechanisms in terms of neural networks in insects. We also review recent advances in the neural mechanisms underlying photoperiodic responses in insects and snails, and additionally circadian clock systems in snails, whose involvement in photoperiodism has hardly been addressed yet. Brain neurosecretory cells, insulin-like peptide/diuretic hormone44-expressing pars intercerebralis neurones in the bean bug Riptortus pedestris and caudo-dorsal cell hormone-expressing caudo-dorsal cells in the snail Lymnaea stagnalis, both promote egg laying under long days, and their electrical excitability is attenuated under short and medium days, which reduces oviposition. The photoperiodic responses of the pars intercerebralis neurones are mediated by glutamate under the control of the clock gene period. Thus, we are now able to assess the photoperiodic response by neurosecretory cell activity to investigate the upstream mechanisms, that is, the photoperiodic clock and counter.

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昆虫和蜗牛基于昼夜节律钟的光周期神经机制
光周期机制区分长日照和短日照,昼夜节律钟系统参与了这一过程。虽然在许多物种中都证明了昼夜节律时钟基因对光周期反应的必要性,但时钟系统如何对光周期机制做出贡献仍不清楚。要了解其分子和细胞机制,必须进行全面的研究,包括相关基因的功能分析及其表达细胞的生理学研究。由于黑腹果蝇表现出较浅层的光周期性,人们从脑部显微手术和神经解剖学入手,在非模式物种中对光周期机制进行了研究,随后对一些昆虫进行了遗传操作。在这里,我们从昆虫神经网络的角度回顾和讨论了昼夜节律钟参与光周期机制的情况。我们还回顾了昆虫和蜗牛光周期反应神经机制的最新进展,以及蜗牛昼夜节律钟系统的最新进展。豆虫的脑神经分泌细胞--表达胰岛素样肽/利尿激素44的间脑旁神经元和蜗牛的表达尾背细胞激素的尾背细胞--在长日照下都会促进产卵,而在短日照和中日照下,它们的电兴奋性会减弱,从而减少产卵。小脑旁神经元的光周期反应是在时钟基因周期的控制下由谷氨酸介导的。因此,我们现在能够通过神经分泌细胞的活动来评估光周期反应,从而研究上游机制,即光周期时钟和计数器。
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来源期刊
CiteScore
4.80
自引率
14.30%
发文量
67
审稿时长
1 months
期刊介绍: The Journal of Comparative Physiology A welcomes original articles, short reviews, and short communications in the following fields: - Neurobiology and neuroethology - Sensory physiology and ecology - Physiological and hormonal basis of behavior - Communication, orientation, and locomotion - Functional imaging and neuroanatomy Contributions should add to our understanding of mechanisms and not be purely descriptive. The level of organization addressed may be organismic, cellular, or molecular. Colour figures are free in print and online.
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