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Temperature-Induced uncoupling of cell cycle regulators.
Falahati, Hanieh; Hur, Woonyung; Di Talia, Stefano; Wieschaus, Eric.
Affiliation
  • Falahati H; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, USA.
  • Hur W; Department of Cell Biology, Duke University Medical Center, Durham, NC, 27710, USA.
  • Di Talia S; Department of Cell Biology, Duke University Medical Center, Durham, NC, 27710, USA.
  • Wieschaus E; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, USA; Howard Hughes Medical Institute, Department of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA. Electronic address: efw@princeton.edu.
Dev Biol ; 470: 147-153, 2021 02.
Article in En | MEDLINE | ID: mdl-33278404
ABSTRACT
The early stages of development involve complex sequences of morphological changes that are both reproducible from embryo to embryo and often robust to environmental variability. To investigate the relationship between reproducibility and robustness we examined cell cycle progression in early Drosophila embryos at different temperatures. Our experiments show that while the subdivision of cell cycle steps is conserved across a wide range of temperatures (5-35 â€‹°C), the relative duration of individual steps varies with temperature. We find that the transition into prometaphase is delayed at lower temperatures relative to other cell cycle events, arguing that it has a different mechanism of regulation. Using an in vivo biosensor, we quantified the ratio of activities of the major mitotic kinase, Cdk1 and one of the major mitotic phosphatases PP1. Comparing activation profile with cell cycle transition times at different temperatures indicates that in early fly embryos activation of Cdk1 drives entry into prometaphase but is not required for earlier cell cycle events. In fact, chromosome condensation can still occur when Cdk1 activity is inhibited pharmacologically. These results demonstrate that different kinases are rate-limiting for different steps of mitosis, arguing that robust inter-regulation may be needed for rapid and ordered mitosis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Cycle / CDC2 Protein Kinase / Drosophila Proteins / Embryo, Nonmammalian / Cell Cycle Checkpoints / Mitosis Limits: Animals Language: En Journal: Dev Biol Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Cycle / CDC2 Protein Kinase / Drosophila Proteins / Embryo, Nonmammalian / Cell Cycle Checkpoints / Mitosis Limits: Animals Language: En Journal: Dev Biol Year: 2021 Document type: Article Affiliation country: United States