Corazonin mediates photoperiodically-induced diapause in the bean bug Riptortus pedestris

滞育 生物 光周期性 神经肽 内科学 内分泌学 生物钟 卵巢 昼夜节律 细胞生物学 植物 受体 遗传学 幼虫 医学
作者
Jili Xi,Yoshitaka Hamanaka,Sakiko Shiga
出处
期刊:The Journal of Experimental Biology [The Company of Biologists]
标识
DOI:10.1242/jeb.250528
摘要

Insects in mid- to high latitudes predict unfavorable seasons through changing photoperiod, and undergo diapause to survive harsh conditions. The circadian clock and brain neurosecretory systems are key components in regulating photoperiodic diapause. However, the neuronal pathways linking these systems, and the neuropeptides involved in photoperiodic diapause remain poorly understood. We have investigated the role of corazonin (CRZ), a conserved neuropeptide regulating metabolic stress and reproduction, in the bean bug Riptortus pedestris, a species highly sensitive to short days for diapause induction. RNA interference demonstrated that Crz-downregulated females significantly averted diapausing phenotypes even under short-day conditions, exhibiting developed ovaries and oviposition, indicating the suppressive effects of Crz on reproduction in photoperiodic diapause. Immunohistochemistry identified three distinct groups of CRZ-immunoreactive (-ir) neurons in the brain. Of these, CRZ-d cells in the pars lateralis (PL) project axons toward the corpus cardiacum-corpus allatum complex and aorta, indicating a neurosecretory role in diapause induction. Additionally, we revealed potential neural connections between CRZ-ir and pigment-dispersing factor (PDF)-ir neurons in the dorso-lateral protocerebrum. The PDF-ir neurons project neurites into/near the accessory medulla (AME), a probable hub for circadian clock regulation, suggesting that photoperiodic information processed in the AME is relayed to CRZ-ir PL neurons. PCR detected Crz receptor expression in the fat body and ovary, suggesting that CRZ-d PL neurons regulate reproductive diapause by directly targeting these tissues in response to photoperiodic inputs. These findings illuminate the neuroendocrine mechanisms underlying photoperiodic reproductive diapause in R. pedestris, highlighting the suppressive role of CRZ under short-day conditions.

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