Departamento de Fisiología, Facultad de Biología, Universidad Complutense de Madrid, Spain.
Chronobiol Int. 2012 Jul;29(6):665-73. doi: 10.3109/07420528.2012.686947.
The aim of the present study was to investigate how photocycle and feeding-time cues regulate the daily expression of Per1a, Per2a, Per3, and Cry3 in the goldfish hindgut. For this purpose, we studied the daily rhythmicity of these genes in fish maintained under different lighting conditions and under different feeding regimes (scheduled or not). We also studied whether the timing of just one meal is able to reset the hindgut molecular clock. In a first experiment, randomly fed fish were divided into four groups and kept under different light conditions for 30 d: 12 h light and 12 h dark (12L:12D), an inverted photoperiod (12D:12L), constant darkness (24D), and constant light (24L). In a second study, fish maintained under 24L were divided into four groups fed at different time points for 35 d: (1) fish scheduled-fed once a day (at 10:00 h); (2) fish fed with a 12-h shifted schedule (at 22:00 h), (3) fish fed at 10:00 h throughout the experiment, except the last day when fed at 22:00 h; and (4) a randomly fed group of fish. Fish were sacrificed every 6 h throughout a 24-h cycle. In both experiments, gPer1a, gPer2a, gPer3, and gCry3 transcripts were quantified using Real Time-qPCR in the hindgut. Results show the clock genes gPer1a, gPer2a, and gCry3 are synchronized by both zeitgebers, the photocycle and feeding regime, in goldfish hindgut. Moreover, such clock genes anticipate light-on and food delivery, when these cues appear in a cyclic manner. In the absence of both zeitgebers, gCry3 and gPer2a rhythmicity disappeared. In contrast, the gPer1 rhythm was maintained under 24L and random feeding conditions, but not always, suggesting that food when randomly supplied is able to reset the clock depending on other factors, such as the energetic and metabolic conditions of the fish. The expression of gPer2a was not activated during the light phase of the cycle, suggesting the hindgut of goldfish is a non-direct photosensitive organ. In contrast to the other three genes, gPer3 expression in the goldfish hindgut seemed to be dependent on the timing of the last food delivery, even in the presence of a photocycle. This gene was the only one that maintained daily rhythms under both constant lighting conditions (24D and 24L), although with lower amplitude than when a photocycle was present. This indicates that, although the acrophase (peak time) of the gPer3 expression rhythm seems to be driven by feeding time, there is an interaction of both zeitgebers, food and light, to regulate its expression. In conclusion, present data indicate: (1) the hindgut of goldfish can be synchronized in vivo by both the photocycle and feeding time; (2) food is a potent signal that entrains this peripheral oscillator; and (3) both environmental cues seems to target different elements of the molecular clock.
本研究旨在探讨光周期和摄食时间线索如何调节金鱼后肠中 Per1a、Per2a、Per3 和 Cry3 的日常表达。为此,我们研究了在不同光照条件下和不同摄食制度(定时或不定时)下这些基因的日常节律。我们还研究了仅一顿饭的时间是否能够重置后肠分子钟。在第一个实验中,随机喂食的鱼被分为四组,并在不同的光照条件下保持 30 天:12 小时光照和 12 小时黑暗(12L:12D)、颠倒光周期(12D:12L)、持续黑暗(24D)和持续光照(24L)。在第二项研究中,在 24L 下饲养的鱼被分为四组,在 35 天内不同时间点喂食:(1)每天定时喂食一次(10:00 h);(2)每天 12 小时喂食时间提前(22:00 h);(3)实验期间每天 10:00 h 喂食,但最后一天 22:00 h 喂食;(4)随机喂食的鱼组。在 24 小时周期内,每隔 6 小时处死一次鱼。在这两个实验中,使用 Real Time-qPCR 在金鱼后肠中定量测定 gPer1a、gPer2a、gPer3 和 gCry3 转录物。结果表明,时钟基因 gPer1a、gPer2a 和 gCry3 被光周期和摄食制度这两个 Zeitgeber 同步,在金鱼后肠中。此外,当这些线索以周期性方式出现时,这些时钟基因会预期光的开启和食物的传递。在没有两个 Zeitgeber 的情况下,gCry3 和 gPer2a 的节律消失。相比之下,gPer1 节律在 24L 和随机喂食条件下得以维持,但并非总是如此,这表明随机供应的食物能够根据鱼类的其他因素(如能量和代谢状况)重置时钟。gPer2a 的表达在周期的光照阶段没有被激活,这表明金鱼的后肠是一个非直接感光器官。与其他三个基因相比,金鱼后肠中 gPer3 的表达似乎取决于最后一次食物输送的时间,即使存在光周期也是如此。该基因是唯一一个在恒定光照条件(24D 和 24L)下维持日常节律的基因,尽管其振幅低于存在光周期时。这表明,尽管 gPer3 表达节律的峰时(峰值时间)似乎由摄食时间驱动,但存在光周期和食物这两个 Zeitgeber 的相互作用来调节其表达。总之,目前的数据表明:(1)金鱼的后肠可以通过光周期和摄食时间在体内同步;(2)食物是一种有效的信号,可以使这种外周振荡器同步;(3)两种环境线索似乎都针对分子钟的不同元素。