Molecular insights of circadian rhythm in Chilopoda

Molecular insights of circadian rhythm in Chilopoda

Автор: Malathi R., Janice M.J.

Журнал: Журнал стресс-физиологии и биохимии @jspb

Статья в выпуске: 2 т.20, 2024 года.

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The control of the sleep-wake cycle as well as several physiological and behavioral processes in living things depends on circadian rhythms. Circadian rhythms are regulated by internal biological clocks that coordinate with environmental stimuli like light and temperature. The significance of circadian rhythms in organisms is emphasized because they support the maintenance of equilibrium between internal and external environments. They have an impact on functions like cellular growth, hormone production, reproduction, and tissue regeneration. Melatonin, cortisol, vasopressin, acetylcholine, insulin, leptin, and body temperature all have an impact on the circadian rhythm. The transcriptional and translational feedback loops formed by a network of genes and proteins are thought to represent the biochemical basis of circadian rhythms. Retinal light exposure is the main factor in the circadian clock's regulation. It is said that Chilopods in particular are nocturnal creatures whose circadian cycles are impacted by environmental cues like light and temperature. Chilopods' circadian rhythms influence many facets of their physiology and behavior, and the timing of necrosis, apoptosis, and autophagy in connection to the day/night cycle has been researched in Chilopods. Also described are the experimental techniques and methodologies utilized to explore Chilopoda circadian cycles. These comprise field research and sample collecting, lab studies utilizing histological and histochemical procedures, scanning and transmission electron microscopy, and other staining techniques. The discussion of factors affecting Chilopoda circadian rhythms has a particular emphasis on light-dark cycles and entrainment. Chilopods synchronize their internal clocks with the external light-dark cycles, and exposure to light is essential for this process. The rate of physiological processes and the timing of circadian oscillations are also influenced by temperature, which is another element that affects Chilopoda circadian rhythms. This study gives a broad summary of the traits, biological basis, experimental approaches, and variables affecting Chilopoda circadian rhythms.

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Chilopoda, circadian rhythm, environment cues, hormones, melatonin, day/night cycle

Короткий адрес: https://sciup.org/143182784

IDR: 143182784

Список литературы Molecular insights of circadian rhythm in Chilopoda

  • Archer, S. N., & Oster, H. (2015). How sleep and wakefulness influence circadian rhythmicity: effects of insufficient and mistimed sleep on the animal and human transcriptome. Journal of sleep research, 24(5), 476-493.
  • Bass, J., & Lazar, M. A. (2016). Circadian time signatures of fitness and disease. Science, 354(6315), 994-999. Casper, R. F., & Gladanac, B. (2014). Introduction: circadian rhythm and its disruption: impact on reproductive function. Fertility and sterility, 102(2), 319-320.
  • Chajec, t., Sonakowska, L., & Rost-Roszkowska, M. M. (2014). The fine structure of the midgut epithelium in a centipede, Scolopendra cingulata (Chilopoda, Scolopendridae), with the special emphasis on epithelial regeneration. Arthropod Structure & Development, 43(1), 27-42.
  • Chipman, A. D., Ferrier, D. E., Brena, C., Qu, J., Hughes, D. S., Schröder, R..... & Richards, S. (2014). The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima. PLoS biology, 12(11), e1002005.
  • Cloudsley-Thompson, J. L. (1949). LXXIV.—The significance of migration in Myriapods. Journal of Natural History, 2(24), 947-962.
  • Cloudsley-Thompson, J. L. (1951). Studies in Diurnal Rhythms I. Rhythmic Behaviour in Millipedes. Journal of Experimental Biology, 28(2), 165-172.
  • Elmore, S. (2007). Apoptosis: a review of programmed cell death. Toxicologic pathology, 35(4), 495-516.
  • Haacker, U. (1967). Diurnal rhythmic vertical motion in centipedes (Myriapoda, Diplopoda). Die Naturwissenschaften, 54(13), 346-347.
  • Hastings, M. H., Maywood, E. S., & Brancaccio, M. (2018). Generation of circadian rhythms in the suprachiasmatic nucleus. Nature Reviews Neuroscience, 19(8), 453-469.
  • John Koilraj, A., Marimuthu, G., & Sharma, V. K. (1999). Circadian rhythm in the locomotor activity of a surface-dwelling millipede Syngalobolus sp. Biological Rhythm Research, 30(5), 529-533.
  • Kaminska, K., Wtodarczyk, A., Sonakowska, L., Ostrozka, A., Marchewka, A., & Rost-Roszkowska, M. (2016). Ultrastructure of the salivary glands in Lithobius forficatus (Myriapoda, Chilopoda, Lithobiidae) according to seasonal and circadian rhythms. Arthropod Structure & Development, 45(6), 536-551.
  • Koilraj, A. J., Sharma, V. K., Marimuthu, G., & Chandrashekaran, M. K. (2000). Presence of circadian rhythms in the locomotor activity of a cave-dwelling millipede Glyphiulus cavernicolus sulu (Cambalidae, Spirostreptida). Chronobiology international, 17(6), 757-765.
  • Kurosaka, K., Takahashi, M., Watanabe, N., & Kobayashi, Y. (2003). Silent cleanup of very early apoptotic cells by macrophages. The Journal of Immunology, 171(9), 4672-4679.
  • Lipovsek, S., Novak, T., Janzekovic, F., Sencic, L., & Pabst, M. A. (2004). A contribution to the functional morphology of the midgut gland in phalangiid harvestmen Gyas annulatus and Gyas titanus during their life cycle. Tissue and Cell, 36(4), 275282.
  • Meuti, M. E., & Denlinger, D. L. (2013). Evolutionary links between circadian clocks and photoperiodic diapause in insects. Integrative and Comparative Biology, 53(1), 131-143.
  • Mohawk, J. A., Green, C. B., & Takahashi, J. S. (2012). Central and peripheral circadian clocks in mammals. Annual review of neuroscience, 35, 445462.
  • Norbury, C. J., & Hickson, I. D. (2001). Cellular responses to DNA damage. Annual review of pharmacology and toxicology, 41(1), 367-401.
  • Park, Y. E., Hayashi, Y. K., Bonne, G., Arimura, T., Noguchi, S., Nonaka, I., & Nishino, I. (2009). Autophagic degradation of nuclear components in mammalian cells. Autophagy, 5(6), 795-804.
  • Partch, C. L., Green, C. B., & Takahashi, J. S. (2014). Molecular architecture of the mammalian circadian clock. Trends in cell biology, 24(2), 90-99.
  • Reddy, A. B., Wong, G. K., O'Neill, J., Maywood, E. S., & Hastings, M. H. (2005). Circadian clocks: neural and peripheral pacemakers that impact upon the cell division cycle. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 574(1-2), 76-91.
  • Reppert, S. M., & Weaver, D. R. (2001). Molecular analysis of mammalian circadian rhythms. Annual review of physiology, 63(1), 647-676.
  • Rost-Roszkowska, M. M., Chajec, t., Vilimova, J., & Tajovsky, K. (2016). Apoptosis and necrosis during the circadian cycle in the centipede midgut. Protoplasma, 253, 1051-1061.
  • Rost-Roszkowska, M. M., Vilimova, J., Tajovsky, K., & Kszuk-Jendrysik, M. (2015). Does autophagy in the midgut epithelium of centipedes depend on the day/night cycle?. Micron, 68, 130-139.
  • Sollars, P. J., & Pickard, G. E. (2015). The neurobiology of circadian rhythms. Psychiatric Clinics, 38(4), 645-665.
  • Szymczak, J. T. (1989). Influence of environmental temperature and photoperiod on temporal structure of sleep in corvids. Acta Neurobiol Exp, 49, 359366.
  • Takahashi, J. S. (2017). Transcriptional architecture of the mammalian circadian clock. Nature Reviews Genetics, 18(3), 164-179.
  • Tanaka, K., & Watari, Y. (2020). Circadian rhythm in locomotor activity of the common house centipede, Thereuonema tuberculata (Scutigeromorha: Scutigeridae). Acta Arachnologica, 69(1), 31-35.
  • Tuf, I. H., Tufovâ, J., Jerâbkovâ, E., & Dedek, P. (2006). Diurnal epigeic activity of myriapods (Chilopoda, Diplopoda). Norwegian Journal of Entomology, 53, 335-344.
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