Mechanisms of Mitotic Spindle Orientation in Mammalian Cells

Information

  • Research Project
  • 7488510
  • ApplicationId
    7488510
  • Core Project Number
    R01GM079506
  • Full Project Number
    5R01GM079506-02
  • Serial Number
    79506
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/2007 - 16 years ago
  • Project End Date
    8/31/2012 - 11 years ago
  • Program Officer Name
    DEATHERAGE, JAMES F.
  • Budget Start Date
    9/1/2008 - 15 years ago
  • Budget End Date
    8/31/2009 - 14 years ago
  • Fiscal Year
    2008
  • Support Year
    2
  • Suffix
  • Award Notice Date
    8/29/2008 - 15 years ago

Mechanisms of Mitotic Spindle Orientation in Mammalian Cells

[unreadable] DESCRIPTION (provided by applicant): The long-term goal of this project is to understand the molecular mechanisms underlying mitotic spindle orientation in mammalian cells. The position of the mitotic spindle determines the direction of chromosome segregation and subsequent cleavage plane of the mother cell. Coordinated cell polarization and spindle orientation plays critical roles during morphogenesis in regulating organ size and shape. It is also the foundation for asymmetric cell division, which allows the daughter cells to inherit different cell fate determinants, a process that is crucial for stem cell function. Perturbation of stem cell function is linked to a wide range of human diseases including neurodegeneration and cancer. Spindle positioning involves the interaction between astral microtubules (MTs) and the cell cortex. Recent studies have revealed the central role played by Pins (LGN and AGS3 in mammals) and the heterotrimeric G protein alpha subunit (Ga) in regulating spindle orientation during asymmetric cell division, but how they are targeted to and maintained at the cell cortex and how they direct spindle orientation remain largely unknown. Recently, we identified a cortical NuMA/LGN/Ga protein complex which can exert forces on astral MTs during mitosis. How is this complex coupled to actin cytoskeleton which is required for the cortical localization of LGN? What forms the phisical link between this complex and astral MTs? We found that filamin-A, an actin binding protein, binds to NuMA, and that cytoplasmic dynein, the minus-end-directed microtubule-based motor protein, interacts with LGN. Based on these preliminary results, we plan to further study the targeting and force generating mechanisms for the corical NuMA/LGN/Ga complex and propose the following specific aims: 1) analyze the dynamics of cortical LGN and NuMA; 2) test the hypothesis that filamih-A is required for cortical targeting or maintenance of LGN during mitosis; 3) test the hypothesis that LGN exerts forces on astral MTs through a direct interaction with cytoplasmic dynein, and that this interaction is regulated by Ga; 4) Analyze the effects of cortical LGN/Ga on microtubule dynamics and test whether dynein mediates these effects. Results from the proposed studies will advance our understanding of the molecular mechanisms by which spindle orientation and asymmetric cell division are achieved in mammalian cells. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    264600
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIGMS:264600\
  • Funding Mechanism
  • Study Section
    CSF
  • Study Section Name
    Cell Structure and Function Study Section
  • Organization Name
    MEDICAL COLLEGE OF GEORGIA (MCG)
  • Organization Department
    NEUROLOGY
  • Organization DUNS
  • Organization City
    AUGUSTA
  • Organization State
    GA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    30912
  • Organization District
    UNITED STATES