Bhat Umer Saleem, Surendran Siju, Sharanya H, Liu Jun, Xu Yun, Tasnim Namra, Bhardwaj Ashwani, Scholz Monika, Babu Kavita
Centre for Neuroscience, Indian Institute of Science (IISc), Bangalore, Karnataka, India.
Department of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, SAS Nagar, Manauli, Punjab, India.
bioRxiv. 2025 May 8:2025.05.02.651881. doi: 10.1101/2025.05.02.651881.
Foraging is essential for sustenance and well-being of all organisms. The transition from well-fed to food-deprived conditions in triggers a localized exploration of the environment characterized by frequent reorientations. However, over time the cumulative frequency of these reorientations decreases, facilitating the transition to global search behaviour. To investigate the genetic regulation of foraging in , we conducted a screen of neuropeptide mutants and identified several candidates involved in modulating this behaviour. Among these, neuropeptide FLP-15 emerged as a key regulator of both local and global search behaviours. Our observations revealed that FLP-15 regulates the frequency and duration of reversals during foraging. Further investigation indicated that FLP-15 is expressed in and functions through the I2 pharyngeal neuron via the G-protein coupled receptor NPR-3. Mutants lacking either or displayed a significant decrease in reversal frequency during local search behaviours. Interestingly, unlike wild-type animals, the reversal frequency in and mutants did not decrease over time. This study also describes the expression pattern of NPR-3, in a subset of head neurons, predominantly comprising of dopaminergic neurons. This expression pattern highlights a potential link between neuropeptide signalling and dopaminergic modulation of behaviour. Finally, exogenous dopamine supplementation assays revealed that FLP-15 may regulate foraging by modulating dopamine transmission, highlighting a novel neuropeptide-dopamine interaction involved in the control of foraging behaviours.
觅食对于所有生物体的生存和健康至关重要。从饱腹状态转变为食物匮乏状态会引发对环境的局部探索,其特征是频繁重新定向。然而,随着时间的推移,这些重新定向的累积频率会降低,从而促进向全局搜索行为的转变。为了研究[具体生物名称]觅食行为的遗传调控,我们对神经肽突变体进行了筛选,并鉴定出了几个参与调节这种行为的候选基因。其中,神经肽FLP - 15成为局部和全局搜索行为的关键调节因子。我们的观察结果表明,FLP - 15调节觅食过程中反转的频率和持续时间。进一步研究表明,FLP - 15通过G蛋白偶联受体NPR - 3在I2咽神经元中表达并发挥作用。缺乏[具体基因名称1]或[具体基因名称2]的突变体在局部搜索行为期间的反转频率显著降低。有趣的是,与野生型动物不同,[具体基因名称1]和[具体基因名称2]突变体的反转频率不会随时间降低。这项研究还描述了NPR - 3在一部分头部神经元中的表达模式,这些神经元主要由多巴胺能神经元组成。这种表达模式突出了神经肽信号传导与行为的多巴胺能调节之间的潜在联系。最后,外源性多巴胺补充实验表明,FLP - 15可能通过调节多巴胺传递来调节觅食行为,突出了一种参与觅食行为控制的新型神经肽 - 多巴胺相互作用。