49
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The Chlamydomonas cell cycle

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          The position of Chlamydomonas within the eukaryotic phylogeny makes it a unique model in at least two important ways: as a representative of the critically important, early‐diverging lineage leading to plants; and as a microbe retaining important features of the last eukaryotic common ancestor ( LECA) that has been lost in the highly studied yeast lineages. Its cell biology has been studied for many decades and it has well‐developed experimental genetic tools, both classical (Mendelian) and molecular. Unlike land plants, it is a haploid with very few gene duplicates, making it ideal for loss‐of‐function genetic studies. The Chlamydomonas cell cycle has a striking temporal and functional separation between cell growth and rapid cell division, probably connected to the interplay between diurnal cycles that drive photosynthetic cell growth and the cell division cycle; it also exhibits a highly choreographed interaction between the cell cycle and its centriole–basal body–flagellar cycle. Here, we review the current status of studies of the Chlamydomonas cell cycle. We begin with an overview of cell‐cycle control in the well‐studied yeast and animal systems, which has yielded a canonical, well‐supported model. We discuss briefly what is known about similarities and differences in plant cell‐cycle control, compared with this model. We next review the cytology and cell biology of the multiple‐fission cell cycle of Chlamydomonas. Lastly, we review recent genetic approaches and insights into Chlamydomonas cell‐cycle regulation that have been enabled by a new generation of genomics‐based tools.

          Significance Statement

          Chlamydomonas is an excellent model for many areas of eukaryotic biology, including the cell cycle. Its phylogenetic position in the green lineage and its utility as a microbial genetic system give this organism great potential for addressing unanswered questions about eukaryotic cell cycle control and for defining new regulatory mechanisms that govern cell cycle progression.

          Related collections

          Most cited references129

          • Record: found
          • Abstract: found
          • Article: not found

          The spindle-assembly checkpoint in space and time.

          In eukaryotes, the spindle-assembly checkpoint (SAC) is a ubiquitous safety device that ensures the fidelity of chromosome segregation in mitosis. The SAC prevents chromosome mis-segregation and aneuploidy, and its dysfunction is implicated in tumorigenesis. Recent molecular analyses have begun to shed light on the complex interaction of the checkpoint proteins with kinetochores--structures that mediate the binding of spindle microtubules to chromosomes in mitosis. These studies are finally starting to reveal the mechanisms of checkpoint activation and silencing during mitotic progression.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Mitochondrial dynamics and inheritance during cell division, development and disease.

            During cell division, it is critical to properly partition functional sets of organelles to each daughter cell. The partitioning of mitochondria shares some common features with that of other organelles, particularly in the use of interactions with cytoskeletal elements to facilitate delivery to the daughter cells. However, mitochondria have unique features - including their own genome and a maternal mode of germline transmission - that place additional demands on this process. Consequently, mechanisms have evolved to regulate mitochondrial segregation during cell division, oogenesis, fertilization and tissue development, as well as to ensure the integrity of these organelles and their DNA, including fusion-fission dynamics, organelle transport, mitophagy and genetic selection of functional genomes. Defects in these processes can lead to cell and tissue pathologies.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Building a cell cycle oscillator: hysteresis and bistability in the activation of Cdc2.

              In the early embryonic cell cycle, Cdc2-cyclin B functions like an autonomous oscillator, whose robust biochemical rhythm continues even when DNA replication or mitosis is blocked. At the core of the oscillator is a negative feedback loop; cyclins accumulate and produce active mitotic Cdc2-cyclin B; Cdc2 activates the anaphase-promoting complex (APC); the APC then promotes cyclin degradation and resets Cdc2 to its inactive, interphase state. Cdc2 regulation also involves positive feedback, with active Cdc2-cyclin B stimulating its activator Cdc25 (refs 5-7) and inactivating its inhibitors Wee1 and Myt1 (refs 8-11). Under the correct circumstances, these positive feedback loops could function as a bistable trigger for mitosis, and oscillators with bistable triggers may be particularly relevant to biological applications such as cell cycle regulation. Therefore, we examined whether Cdc2 activation is bistable. We confirm that the response of Cdc2 to non-degradable cyclin B is temporally abrupt and switch-like, as would be expected if Cdc2 activation were bistable. We also show that Cdc2 activation exhibits hysteresis, a property of bistable systems with particular relevance to biochemical oscillators. These findings help establish the basic systems-level logic of the mitotic oscillator.
                Bookmark

                Author and article information

                Journal
                Plant J
                Plant J
                10.1111/(ISSN)1365-313X
                TPJ
                The Plant Journal
                John Wiley and Sons Inc. (Hoboken )
                0960-7412
                1365-313X
                15 April 2015
                May 2015
                : 82
                : 3 , Chlamydomonas ( doiID: 10.1111/tpj.2015.82.issue-3 )
                : 370-392
                Affiliations
                [ 1 ]The Rockefeller University New York NY 10065USA
                [ 2 ]Donald Danforth Plant Science Center St. Louis MO 63132USA
                Author notes
                [*] [* ]For correspondence (e‐mail: jumen@ 123456danforthcenter.org ).
                Article
                TPJ12795
                10.1111/tpj.12795
                4409525
                25690512
                ce2bcf25-d3f8-47f0-9046-4ab02ccd3242
                © 2015 The Authors The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 09 December 2014
                : 03 February 2015
                : 04 February 2015
                Page count
                Pages: 23
                Funding
                Funded by: National Institutes of Health (NIH)
                Award ID: 5R01GM078153‐07
                Award ID: 1R0 GM078376
                Categories
                SI Chlamydomonas
                Chlamydomonas
                Custom metadata
                2.0
                tpj12795
                May 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:01.09.2016

                Plant science & Botany
                chlamydomonas reinhardtii,phycoplast,multiple fission,cell‐cycle mutant,mitosis,cytokinesis,volvocine algae

                Comments

                Comment on this article