scholarly journals Hypothermia modulates circadian clock gene expression in lizard peripheral tissues

2007 ◽  
Vol 292 (1) ◽  
pp. R160-R166 ◽  
Author(s):  
Daniela Vallone ◽  
Elena Frigato ◽  
Cristiano Vernesi ◽  
Augusto Foà ◽  
Nicholas S. Foulkes ◽  
...  

The molecular mechanisms whereby the circadian clock responds to temperature changes are poorly understood. The ruin lizard Podarcis sicula has historically proven to be a valuable vertebrate model for exploring the influence of temperature on circadian physiology. It is an ectotherm that naturally experiences an impressive range of temperatures during the course of the year. However, no tools have been available to dissect the molecular basis of the clock in this organism. Here, we report the cloning of three lizard clock gene homologs ( Period2, Cryptochrome1, and Clock) that have a close phylogenetic relationship with avian clock genes. These genes are expressed in many tissues and show a rhythmic expression profile at 29°C in light-dark and constant darkness lighting conditions, with phases comparable to their mammalian and avian counterparts. Interestingly, we show that at low temperatures (6°C), cycling clock gene expression is attenuated in peripheral clocks with a characteristic increase in basal expression levels. We speculate that this represents a conserved vertebrate clock gene response to low temperatures. Furthermore, these results bring new insight into the issue of whether circadian clock function is compatible with hypothermia.

2007 ◽  
Vol 26 (10) ◽  
pp. 2731-2738 ◽  
Author(s):  
Mitsugu Sujino ◽  
Mamoru Nagano ◽  
Atsuko Fujioka ◽  
Yasufumi Shigeyoshi ◽  
Shin-Ichi T. Inouye

2019 ◽  
Author(s):  
Sarah C. Markt ◽  
Ericka Ebot ◽  
Iona Cheng ◽  
Lynne Wilkens ◽  
Ayesha Shafi ◽  
...  

2013 ◽  
Vol 29 (4) ◽  
pp. 331-335 ◽  
Author(s):  
Kalliopi I. Pappa ◽  
Maria Gazouli ◽  
Eleni Anastasiou ◽  
Zoe Iliodromiti ◽  
Aristides Antsaklis ◽  
...  

2019 ◽  
Author(s):  
M Schlichting ◽  
MM Diaz ◽  
J Xin ◽  
M Rosbash

AbstractAnimal circadian rhythms persist in constant darkness and are driven by intracellular transcription-translation feedback loops. Although these cellular oscillators communicate, isolated mammalian cellular clocks continue to tick away in darkness without intercellular communication. To investigate these issues in Drosophila, we assayed behavior as well as molecular rhythms within individual brain clock neurons while blocking communication within the ca. 150 neuron clock network. We also generated CRISPR-mediated neuron-specific circadian clock knockouts. The results point to two key clock neuron groups: loss of the clock within both regions but neither one alone has a strong behavioral phenotype in darkness; communication between these regions also contributes to circadian period determination. Under these dark conditions, the clock within one region persists without network communication. The clock within the famous PDF-expressing s-LNv neurons however was strongly dependent on network communication, likely because clock gene expression within these vulnerable sLNvs depends on neuronal firing or light.


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