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Chlamydomonas reinhardtii: duration of its cell cycle and phases at growth rates affected by light intensity
M. Vítová, K. Bišová, D. Umysová, M. Hlavová, S. Kawano, V. Zachleder, M. Cížková
Language English Country Germany
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
ProQuest Central
from 2002-11-01 to 1 year ago
Medline Complete (EBSCOhost)
from 1999-11-01 to 1 year ago
Health & Medicine (ProQuest)
from 2002-11-01 to 1 year ago
- MeSH
- Cell Cycle radiation effects MeSH
- Time Factors MeSH
- Chlamydomonas reinhardtii cytology growth & development radiation effects MeSH
- Period Circadian Proteins metabolism MeSH
- Circadian Rhythm genetics radiation effects MeSH
- Cells, Cultured MeSH
- Mutation genetics MeSH
- Light MeSH
- Darkness MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
In the cultures of the alga Chlamydomonas reinhardtii, division rhythms of any length from 12 to 75 h were found at a range of different growth rates that were set by the intensity of light as the sole source of energy. The responses to light intensity differed in terms of altered duration of the phase from the beginning of the cell cycle to the commitment to divide, and of the phase after commitment to cell division. The duration of the pre-commitment phase was determined by the time required to attain critical cell size and sufficient energy reserves (starch), and thus was inversely proportional to growth rate. If growth was stopped by interposing a period of darkness, the pre-commitment phase was prolonged corresponding to the duration of the dark interval. The duration of the post-commitment phase, during which the processes leading to cell division occurred, was constant and independent of growth rate (light intensity) in the cells of the same division number, or prolonged with increasing division number. It appeared that different regulatory mechanisms operated through these two phases, both of which were inconsistent with gating of cell division at any constant time interval. No evidence was found to support any hypothetical timer, suggested to be triggered at the time of daughter cell release.
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