Literature DB >> 36173529

Variations in Circadian Clock Organization & Function: A Journey from Ancient to Recent.

Alena Patnaik1, Hemasundar Alavilli2, Jnanendra Rath3, Kishore C S Panigrahi1, Madhusmita Panigrahy4.   

Abstract

MAIN
CONCLUSION: Circadian clock components exhibit structural variations in different plant systems, and functional variations during various abiotic stresses. These variations bear relevance for plant fitness and could be important evolutionarily. All organisms on earth have the innate ability to measure time as diurnal rhythms that occur due to the earth's rotations in a 24-h cycle. Circadian oscillations arising from the circadian clock abide by its fundamental properties of periodicity, entrainment, temperature compensation, and oscillator mechanism, which is central to its function. Despite the fact that a myriad of research in Arabidopsis thaliana illuminated many detailed aspects of the circadian clock, many more variations in clock components' organizations and functions remain to get deciphered. These variations are crucial for sustainability and adaptation in different plant systems in the varied environmental conditions in which they grow. Together with these variations, circadian clock functions differ drastically even during various abiotic and biotic stress conditions. The present review discusses variations in the organization of clock components and their role in different plant systems and abiotic stresses. We briefly introduce the clock components, entrainment, and rhythmicity, followed by the variants of the circadian clock in different plant types, starting from lower non-flowering plants, marine plants, dicots to the monocot crop plants. Furthermore, we discuss the interaction of the circadian clock with components of various abiotic stress pathways, such as temperature, light, water stress, salinity, and nutrient deficiency with implications for the reprogramming during these stresses. We also update on recent advances in clock regulations due to post-transcriptional, post-translation, non-coding, and micro-RNAs. Finally, we end this review by summarizing the points of applicability, a remark on the future perspectives, and the experiments that could clear major enigmas in this area of research.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Abiotic stress; Circadian clock; Circadian rhythm; Diurnal rhythm; Nutritional deficiency; Post-transcriptional

Mesh:

Substances:

Year:  2022        PMID: 36173529     DOI: 10.1007/s00425-022-04002-1

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.540


  157 in total

1.  Arabidopsis FHY3 specifically gates phytochrome signaling to the circadian clock.

Authors:  Trudie Allen; Athanasios Koustenis; George Theodorou; David E Somers; Steve A Kay; Garry C Whitelam; Paul F Devlin
Journal:  Plant Cell       Date:  2006-09-29       Impact factor: 11.277

2.  Cycling vrille expression is required for a functional Drosophila clock.

Authors:  J Blau; M W Young
Journal:  Cell       Date:  1999-12-10       Impact factor: 41.582

3.  Photoperiod sensing of the circadian clock is controlled by EARLY FLOWERING 3 and GIGANTEA.

Authors:  Muhammad Usman Anwer; Amanda Davis; Seth Jon Davis; Marcel Quint
Journal:  Plant J       Date:  2019-12-11       Impact factor: 6.417

Review 4.  Light and temperature cues: multitasking receptors and transcriptional integrators.

Authors:  Jorge J Casal; Julia I Qüesta
Journal:  New Phytol       Date:  2017-11-15       Impact factor: 10.151

5.  Involvement of GIGANTEA gene in the regulation of the cold stress response in Arabidopsis.

Authors:  Shuqing Cao; Ming Ye; Shaotong Jiang
Journal:  Plant Cell Rep       Date:  2005-10-18       Impact factor: 4.570

Review 6.  Circadian coordination of cellular processes and abiotic stress responses.

Authors:  Titouan Bonnot; Emily J Blair; Samantha J Cordingley; Dawn H Nagel
Journal:  Curr Opin Plant Biol       Date:  2021-11-10       Impact factor: 7.834

7.  A pseudo-response regulator is misexpressed in the photoperiod insensitive Ppd-D1a mutant of wheat (Triticum aestivum L.).

Authors:  James Beales; Adrian Turner; Simon Griffiths; John W Snape; David A Laurie
Journal:  Theor Appl Genet       Date:  2007-07-19       Impact factor: 5.699

8.  ELF3 controls thermoresponsive growth in Arabidopsis.

Authors:  Mathew S Box; B Emma Huang; Mirela Domijan; Katja E Jaeger; Asif Khan Khattak; Seong Jeon Yoo; Emma L Sedivy; D Marc Jones; Timothy J Hearn; Alex A R Webb; Alastair Grant; James C W Locke; Philip A Wigge
Journal:  Curr Biol       Date:  2014-12-31       Impact factor: 10.834

9.  AtGRP7 is involved in the regulation of abscisic acid and stress responses in Arabidopsis.

Authors:  Shuqing Cao; Li Jiang; Shiyong Song; Ran Jing; Guosheng Xu
Journal:  Cell Mol Biol Lett       Date:  2006-09-26       Impact factor: 5.787

10.  Organ specificity in the plant circadian system is explained by different light inputs to the shoot and root clocks.

Authors:  Simon Bordage; Stuart Sullivan; Janet Laird; Andrew J Millar; Hugh G Nimmo
Journal:  New Phytol       Date:  2016-05-31       Impact factor: 10.151

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