Literature DB >> 18583942

Coordination of mitochondrial bioenergetics with G1 phase cell cycle progression.

Stefan M Schieke1, J Philip McCoy, Toren Finkel.   

Abstract

Relatively little is known regarding how energetic demand during cell proliferation is sensed or coordinated with mitochondrial metabolism. Here we demonstrate that cell cycle progression through G(1) is associated with a significant increase in mitochondrial membrane potential (DeltaPsi(m)) and respiration. We used this change in metabolic rate to isolate cells in G(1) with low and high levels of mitochondrial membrane potential (DeltaPsi(m)L and DeltaPsi(m)H). Biochemical and functional studies demonstrate that DeltaPsi(m)L and DeltaPsi(m)H cells display the distinct characteristics of early and late G(1) phase, respectively. We further demonstrate that the metabolic rate in G(1) reflects levels of the mTOR-raptor complex as well as susceptibility to rapamycin-induced cell cycle delay. In conclusion, our data suggests a coupling of mitochondrial bioenergetics and G(1) progression and points to the mTOR signaling pathway as a potential molecular coordinator of these two processes.

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Year:  2008        PMID: 18583942      PMCID: PMC3399174          DOI: 10.4161/cc.7.12.6067

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  16 in total

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2.  A restriction point for control of normal animal cell proliferation.

Authors:  A B Pardee
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4.  Insights into TOR function and rapamycin response: chemical genomic profiling by using a high-density cell array method.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-09       Impact factor: 11.205

5.  Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast.

Authors:  J Heitman; N R Movva; M N Hall
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6.  The mammalian target of rapamycin (mTOR) pathway regulates mitochondrial oxygen consumption and oxidative capacity.

Authors:  Stefan M Schieke; Darci Phillips; J Philip McCoy; Angel M Aponte; Rong-Fong Shen; Robert S Balaban; Toren Finkel
Journal:  J Biol Chem       Date:  2006-07-17       Impact factor: 5.157

7.  Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton.

Authors:  D D Sarbassov; Siraj M Ali; Do-Hyung Kim; David A Guertin; Robert R Latek; Hediye Erdjument-Bromage; Paul Tempst; David M Sabatini
Journal:  Curr Biol       Date:  2004-07-27       Impact factor: 10.834

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Authors:  J Chung; C J Kuo; G R Crabtree; J Blenis
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9.  mTOR controls mitochondrial oxidative function through a YY1-PGC-1alpha transcriptional complex.

Authors:  John T Cunningham; Joseph T Rodgers; Daniel H Arlow; Francisca Vazquez; Vamsi K Mootha; Pere Puigserver
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10.  mTOR interacts with raptor to form a nutrient-sensitive complex that signals to the cell growth machinery.

Authors:  Do-Hyung Kim; D D Sarbassov; Siraj M Ali; Jessie E King; Robert R Latek; Hediye Erdjument-Bromage; Paul Tempst; David M Sabatini
Journal:  Cell       Date:  2002-07-26       Impact factor: 41.582

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Authors:  Toren Finkel; Paul M Hwang
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6.  Induction of autophagy supports the bioenergetic demands of quiescent muscle stem cell activation.

Authors:  Ann H Tang; Thomas A Rando
Journal:  EMBO J       Date:  2014-10-14       Impact factor: 11.598

7.  Delayed correlation of mRNA and protein expression in rapamycin-treated cells and a role for Ggc1 in cellular sensitivity to rapamycin.

Authors:  Marjorie L Fournier; Ariel Paulson; Norman Pavelka; Amber L Mosley; Karin Gaudenz; William D Bradford; Earl Glynn; Hua Li; Mihaela E Sardiu; Brian Fleharty; Christopher Seidel; Laurence Florens; Michael P Washburn
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9.  PGC-1-related coactivator modulates mitochondrial-nuclear crosstalk through endogenous nitric oxide in a cellular model of oncocytic thyroid tumours.

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10.  Nutrition controls mitochondrial biogenesis in the Drosophila adipose tissue through Delg and cyclin D/Cdk4.

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Journal:  PLoS One       Date:  2009-09-09       Impact factor: 3.240

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