Kotwica-Rolinska Joanna, Damulewicz Milena, Chodakova Lenka, Kristofova Lucie, Dolezel David
Institute of Entomology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic.
Institute of Zoology and Biomedical Research, Jagiellonian University, Kraków, Poland.
Front Physiol. 2022 Apr 29;13:884909. doi: 10.3389/fphys.2022.884909. eCollection 2022.
Daily and annually cycling conditions manifested on the Earth have forced organisms to develop time-measuring devices. Circadian clocks are responsible for adjusting physiology to the daily cycles in the environment, while the anticipation of seasonal changes is governed by the photoperiodic clock. Circadian clocks are cell-autonomous and depend on the transcriptional/translational feedback loops of the conserved clock genes. The synchronization among clock centers in the brain is achieved by the modulatory function of the clock-dependent neuropeptides. In insects, the most prominent clock neuropeptide is Pigment Dispersing Factor (PDF). Photoperiodic clock measures and computes the day and/or night length and adjusts physiology accordingly to the upcoming season. The exact mechanism of the photoperiodic clock and its direct signaling molecules are unknown but, in many insects, circadian clock genes are involved in the seasonal responses. While in , PDF signaling participates both in the circadian clock output and in diapause regulation, the weak photoperiodic response curve of is a major limitation in revealing the full role of PDF in the photoperiodic clock. Here we provide the first description of PDF in the linden bug, , an organism with a robust photoperiodic response. We characterize in detail the circadian and photoperiodic phenotype of several CRISPR/Cas9-generated mutants, including three null mutants and two mutants with modified PDF. Our results show that PDF acts downstream of CRY and plays a key role as a circadian clock output. Surprisingly, in contrast to the diurnal activity of wild-type bugs, null mutants show predominantly nocturnal activity, which is caused by the clock-independent direct response to the light/dark switch. Moreover, we show that together with CRY, PDF is involved in the photoperiod-dependent diapause induction, however, its lack does not disrupt the photoperiodic response completely, suggesting the presence of additional clock-regulated factors. Taken together our data provide new insight into the role of PDF in the insect's circadian and photoperiodic systems.
地球上每日和每年循环出现的环境条件迫使生物体进化出计时装置。昼夜节律时钟负责使生理机能适应环境中的每日周期,而对季节变化的预测则由光周期时钟控制。昼夜节律时钟是细胞自主的,依赖于保守时钟基因的转录/翻译反馈环。大脑中时钟中心之间的同步是通过时钟依赖性神经肽的调节功能实现的。在昆虫中,最突出的时钟神经肽是色素分散因子(PDF)。光周期时钟测量并计算白天和/或夜晚的时长,并据此使生理机能适应即将到来的季节。光周期时钟的确切机制及其直接信号分子尚不清楚,但在许多昆虫中,昼夜节律时钟基因参与了季节性反应。虽然在[此处原文缺失相关昆虫名称]中,PDF信号传导既参与昼夜节律时钟输出,也参与滞育调节,但[此处原文缺失相关昆虫名称]微弱的光周期反应曲线是揭示PDF在光周期时钟中全部作用的主要限制。在这里,我们首次描述了在林登臭虫[此处原文缺失相关昆虫名称]中的PDF,这是一种具有强烈光周期反应的生物体。我们详细表征了几个CRISPR/Cas9基因编辑产生的[此处原文缺失相关昆虫名称]突变体的昼夜节律和光周期表型,包括三个基因敲除突变体和两个PDF修饰突变体。我们的结果表明,PDF在CRY下游起作用,作为昼夜节律时钟输出发挥关键作用。令人惊讶的是,与野生型臭虫的日间活动相反,[此处原文缺失相关昆虫名称]基因敲除突变体主要表现为夜间活动,这是由对光/暗转换的非时钟依赖性直接反应引起的。此外,我们表明,PDF与CRY一起参与光周期依赖性滞育诱导,然而,PDF的缺失并不会完全破坏光周期反应,这表明存在其他时钟调节因子。综上所述,我们的数据为PDF在昆虫昼夜节律和光周期系统中的作用提供了新的见解。