Quiescence: early evolutionary origins and universality do not imply uniformity
- PMID: 22084377
- PMCID: PMC3203459
- DOI: 10.1098/rstb.2011.0079
Quiescence: early evolutionary origins and universality do not imply uniformity
Abstract
Cell cycle investigations have focused on relentless exponential proliferation of cells, an unsustainable situation in nature. Proliferation of cells, whether microbial or metazoan, is interrupted by periods of quiescence. The vast majority of cells in an adult metazoan lie quiescent. As disruptions in this quiescence are at the foundation of cancer, it will be important for the field to turn its attention to the mechanisms regulating quiescence. While often presented as a single topic, there are multiple forms of quiescence each with complex inputs, some of which are tied to conceptually challenging aspects of metazoan regulation such as size control. In an effort to expose the enormity of the challenge, I describe the differing biological purposes of quiescence, and the coupling of quiescence in metazoans to growth and to the structuring of tissues during development. I emphasize studies in the organism rather than in tissue culture, because these expose the diversity of regulation. While quiescence is likely to be a primitive biological process, it appears that in adapting quiescence to its many distinct biological settings, evolution has diversified it. Consideration of quiescence in different models gives us an overview of this diversity.
Similar articles
-
Quiescence, an individual journey.Curr Genet. 2019 Jun;65(3):695-699. doi: 10.1007/s00294-018-00928-w. Epub 2019 Jan 16. Curr Genet. 2019. PMID: 30649583 Review.
-
Development of ichthyosporeans sheds light on the origin of metazoan multicellularity.Dev Biol. 2013 May 1;377(1):284-92. doi: 10.1016/j.ydbio.2013.01.009. Epub 2013 Jan 18. Dev Biol. 2013. PMID: 23333946 Free PMC article.
-
States of G0 and the proliferation-quiescence decision in cells, tissues and during development.Int J Dev Biol. 2017;61(6-7):357-366. doi: 10.1387/ijdb.160343LB. Int J Dev Biol. 2017. PMID: 28695955 Review.
-
Evolutionary Dynamics of the Spindle Assembly Checkpoint in Eukaryotes.Curr Biol. 2020 May 18;30(10):R589-R602. doi: 10.1016/j.cub.2020.02.021. Curr Biol. 2020. PMID: 32428500 Review.
-
Cellular Mechanisms and Regulation of Quiescence.Dev Cell. 2020 Nov 9;55(3):259-271. doi: 10.1016/j.devcel.2020.09.029. Dev Cell. 2020. PMID: 33171109 Free PMC article. Review.
Cited by
-
Non-linear hierarchy of the quorum sensing signalling pathway in bloodstream form African trypanosomes.PLoS Pathog. 2018 Jun 25;14(6):e1007145. doi: 10.1371/journal.ppat.1007145. eCollection 2018 Jun. PLoS Pathog. 2018. PMID: 29940034 Free PMC article.
-
The proliferation-quiescence decision is controlled by a bifurcation in CDK2 activity at mitotic exit.Cell. 2013 Oct 10;155(2):369-83. doi: 10.1016/j.cell.2013.08.062. Epub 2013 Sep 26. Cell. 2013. PMID: 24075009 Free PMC article.
-
An Exportin-1-dependent microRNA biogenesis pathway during human cell quiescence.Proc Natl Acad Sci U S A. 2017 Jun 20;114(25):E4961-E4970. doi: 10.1073/pnas.1618732114. Epub 2017 Jun 5. Proc Natl Acad Sci U S A. 2017. PMID: 28584122 Free PMC article.
-
Growing an Embryo from a Single Cell: A Hurdle in Animal Life.Cold Spring Harb Perspect Biol. 2015 Aug 7;7(11):a019042. doi: 10.1101/cshperspect.a019042. Cold Spring Harb Perspect Biol. 2015. PMID: 26254311 Free PMC article. Review.
-
Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli.Open Biol. 2022 Dec;12(12):220216. doi: 10.1098/rsob.220216. Epub 2022 Dec 21. Open Biol. 2022. PMID: 36541101 Free PMC article.
References
-
- Harding J. D., MacDonald R. J., Przybyla A. E., Chirgwin J. M., Pictet R. L., Rutter W. J. 1977. Changes in the frequency of specific transcripts during development of the pancreas. J. Biol. Chem. 252, 7391–7397 - PubMed
-
- Malthus T. R. 1872. An essay on the principle of population, 7th edn. London, UK: Reeves and Turner.
-
- O'Farrell P. H. 2001. Triggering the all-or-nothing switch into mitosis. Trends Cell Biol. 11, 512–51910.1016/S0962-8924(01)02142-0 (doi:10.1016/S0962-8924(01)02142-0) - DOI - DOI - PMC - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials