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PMID:16326395

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Citation

Mandal, S, Guptan, P, Owusu-Ansah, E and Banerjee, U (2005) Mitochondrial regulation of cell cycle progression during development as revealed by the tenured mutation in Drosophila. Dev. Cell 9:843-54

Abstract

The precise control of the cell cycle requires regulation by many intrinsic and extrinsic factors. Whether the metabolic status of the cell exerts a direct control over cell cycle checkpoints is not well understood. We isolated a mutation, tenured (tend), in a gene encoding cytochrome oxidase subunit Va. This mutation causes a drop in intracellular ATP to levels sufficient to maintain cell survival, growth, and differentiation, but not to enable progression through the cell cycle. Analysis of this gene in vivo and in cell lines shows that a specific pathway involving AMPK and p53 is activated that causes elimination of Cyclin E, resulting in cell cycle arrest. We demonstrate that in multiple tissues the mitochondrion has a direct and specific role in enforcing a G1-S cell cycle checkpoint during periods of energy deprivation.

Links

PubMed Online version:10.1016/j.devcel.2005.11.006

Keywords

AMP-Activated Protein Kinases; Adenosine Triphosphate/metabolism; Animals; Animals, Genetically Modified; Cell Differentiation; Cell Proliferation; Cell Survival; Cyclin E/metabolism; Drosophila melanogaster/genetics; Drosophila melanogaster/growth & development; Drosophila melanogaster/metabolism; Electron Transport Complex IV/genetics; Electron Transport Complex IV/metabolism; Female; G1 Phase; Male; Mitochondria/metabolism; Multienzyme Complexes/metabolism; Mutation; Protein-Serine-Threonine Kinases/metabolism; S Phase; Tumor Suppressor Protein p53/metabolism

Significance

Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status


See also

References

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