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Drosophila Ionotropic Receptor 25a mediates circadian clock resetting by temperature

机译:果蝇离子受体25a通过温度介导生物钟复位

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摘要

Circadian clocks are endogenous timers adjusting behaviour and physiology with the solar day(1). Synchronized circadian clocks improve fitness(2) and are crucial for our physical and mental well-being(3). Visual and non-visual photoreceptors are responsible for synchronizing circadian clocks to light(4,5), but clock-resetting is also achieved by alternating day and night temperatures with only 2-4 degrees C difference(6-8). This temperature sensitivity is remarkable considering that the circadian clock period (similar to 24 h) is largely independent of surrounding ambient temperatures(1,8). Here we show that Drosophila Ionotropic Receptor 25a (IR25a) is required for behavioural synchronization to low-amplitude temperature cycles. This channel is expressed in sensory neurons of internal stretch receptors previously implicated in temperature synchronization of the circadian clock(9). IR25a is required for temperature-synchronized clock protein oscillations in subsets of central clock neurons. Extracellular leg nerve recordings reveal temperature-and IR25a-dependent sensory responses, and IR25a misexpression confers temperature-dependent firing of heterologous neurons. We propose that IR25a is part of an input pathway to the circadian clock that detects small temperature differences. This pathway operates in the absence of known 'hot' and 'cold' sensors in the Drosophila antenna(10,11), revealing the existence of novel periphery-to-brain temperature signalling channels.
机译:昼夜节律钟是内源性的计时器,可以随着太阳日的变化来调节行为和生理(1)。同步生物钟提高健康度(2),对于我们的身心健康至关重要(3)。视觉和非视觉感光器负责使生物钟与光同步(4,5),但时钟的重置也可以通过昼夜温度交替进行,温度差只有2-4摄氏度(6-8)。考虑到昼夜节律时钟周期(类似于24小时)在很大程度上与周围环境温度无关,因此这种温度敏感性非常显着(1,8)。在这里,我们显示果蝇离子受体25a(IR25a)对于低振幅温度周期的行为同步是必需的。该通道在内部牵张受体的感觉神经元中表达,以前牵涉到生物钟的温度同步(9)。 IR25a是中央时钟神经元子集中温度同步时钟蛋白振荡所必需的。细胞外腿神经记录揭示了温度和IR25a依赖性的感觉反应,IR25a的错误表达赋予异源神经元温度依赖性的放电。我们建议IR25a是检测小温差的生物钟输入路径的一部分。该途径在果蝇天线中没有已知的``热''和``冷''传感器的情况下起作用(10,11),这表明存在新颖的外周到大脑温度信号通道。

著录项

  • 来源
    《Nature》 |2015年第7579期|516-520|共5页
  • 作者单位

    UCL, Dept Cell & Dev Biol, London WC1E 6DE, England;

    Univ Bristol, Sch Physiol & Pharmacol, Bristol BS8 1TD, Avon, England;

    UCL, Dept Cell & Dev Biol, London WC1E 6DE, England;

    Univ Lausanne, Fac Biol & Med, Ctr Integrat Genom, CH-1015 Lausanne, Switzerland;

    Univ Cambridge, Cambridge Syst Biol Ctr, Cambridge CB2 1QW, England|Univ Cambridge, Dept Biochem, Cambridge Ctr Prote, Cambridge CB2 1QW, England;

    Univ Cambridge, Cambridge Syst Biol Ctr, Cambridge CB2 1QW, England|Univ Cambridge, Dept Biochem, Cambridge Ctr Prote, Cambridge CB2 1QW, England;

    Univ Lausanne, Fac Biol & Med, Ctr Integrat Genom, CH-1015 Lausanne, Switzerland;

    Univ Bristol, Sch Physiol & Pharmacol, Bristol BS8 1TD, Avon, England;

    UCL, Dept Cell & Dev Biol, London WC1E 6DE, England;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 02:52:43

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