» Articles » PMID: 26335718

Circadian Rhythms in Cyanobacteria

Overview
Specialty Microbiology
Date 2015 Sep 4
PMID 26335718
Citations 111
Authors
Affiliations
Soon will be listed here.
Abstract

Life on earth is subject to daily and predictable fluctuations in light intensity, temperature, and humidity created by rotation of the earth. Circadian rhythms, generated by a circadian clock, control temporal programs of cellular physiology to facilitate adaptation to daily environmental changes. Circadian rhythms are nearly ubiquitous and are found in both prokaryotic and eukaryotic organisms. Here we introduce the molecular mechanism of the circadian clock in the model cyanobacterium Synechococcus elongatus PCC 7942. We review the current understanding of the cyanobacterial clock, emphasizing recent work that has generated a more comprehensive understanding of how the circadian oscillator becomes synchronized with the external environment and how information from the oscillator is transmitted to generate rhythms of biological activity. These results have changed how we think about the clock, shifting away from a linear model to one in which the clock is viewed as an interactive network of multifunctional components that are integrated into the context of the cell in order to pace and reset the oscillator. We conclude with a discussion of how this basic timekeeping mechanism differs in other cyanobacterial species and how information gleaned from work in cyanobacteria can be translated to understanding rhythmic phenomena in other prokaryotic systems.

Citing Articles

Parameterized resetting model captures dose-dependent entrainment of the mouse circadian clock.

Masuda K, Yoshimoto R, Li R, Sakurai T, Hirano A Nat Commun. 2025; 16(1):1421.

PMID: 39915501 PMC: 11802799. DOI: 10.1038/s41467-025-56792-z.


Markovian State Models uncover Casein Kinase 1 dynamics that govern circadian period.

Ricci C, Philpott J, Torgrimson M, Freeberg A, Narasimamurthy R, de Barros E bioRxiv. 2025; .

PMID: 39896482 PMC: 11785140. DOI: 10.1101/2025.01.17.633651.


Programming scheduled self-assembly of circadian materials.

Leech G, Melcher L, Chiu M, Nugent M, Juliano S, Burton L Nat Commun. 2025; 16(1):176.

PMID: 39747896 PMC: 11696221. DOI: 10.1038/s41467-024-55645-5.


Photomorphogenesis of Myxococcus macrosporus: new insights for light-regulation of cell development.

Graniczkowska K, Bizhga D, Noda M, Leon V, Saraf N, Feliz D Photochem Photobiol Sci. 2024; 23(10):1857-1870.

PMID: 39298056 PMC: 11832031. DOI: 10.1007/s43630-024-00635-1.


Two KaiABC systems control circadian oscillations in one cyanobacterium.

Kobler C, Schmelling N, Wiegard A, Pawlowski A, Pattanayak G, Spat P Nat Commun. 2024; 15(1):7674.

PMID: 39227593 PMC: 11372060. DOI: 10.1038/s41467-024-51914-5.


References
1.
Pattanayek R, Wang J, Mori T, Xu Y, Johnson C, Egli M . Visualizing a circadian clock protein: crystal structure of KaiC and functional insights. Mol Cell. 2004; 15(3):375-88. DOI: 10.1016/j.molcel.2004.07.013. View

2.
Kutsuna S, Nakahira Y, Katayama M, Ishiura M, Kondo T . Transcriptional regulation of the circadian clock operon kaiBC by upstream regions in cyanobacteria. Mol Microbiol. 2005; 57(5):1474-84. DOI: 10.1111/j.1365-2958.2005.04781.x. View

3.
Kondo T, Mori T, Lebedeva N, Aoki S, Ishiura M, Golden S . Circadian rhythms in rapidly dividing cyanobacteria. Science. 1997; 275(5297):224-7. DOI: 10.1126/science.275.5297.224. View

4.
Dvornyk V, Vinogradova O, Nevo E . Origin and evolution of circadian clock genes in prokaryotes. Proc Natl Acad Sci U S A. 2003; 100(5):2495-500. PMC: 151369. DOI: 10.1073/pnas.0130099100. View

5.
Nishiwaki T, Satomi Y, Kitayama Y, Terauchi K, Kiyohara R, Takao T . A sequential program of dual phosphorylation of KaiC as a basis for circadian rhythm in cyanobacteria. EMBO J. 2007; 26(17):4029-37. PMC: 1994132. DOI: 10.1038/sj.emboj.7601832. View