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Regulation of Membrane-Cortical Cytoskeleton Crosstalk by WASH

Regulation of Membrane-Cortical Cytoskeleton Crosstalk by WASH
WASH 对膜-皮质细胞骨架串扰的调节
批准号:
8687673
负责人:
SUSAN M PARKHURST
金额:
$35.05万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-07-01 至 2016-06-30

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DESCRIPTION (provided by applicant): The plasma membrane and the underlying cortical cytoskeleton undergo continuous dynamic interplay that is necessary for many essential cellular processes, including signal transduction, migration, endo-/exo-cytosis, and inter- and intra-cellular attachments/adhesion. Thus, the proteins that regulate these interactions and their function are of general importance in biology. The Wiskott Aldrich Syndrome (WAS) protein family, which act as effectors of Rho family GTPases, polymerize actin through the Arp2/3 complex. The two founding WAS family members, WASP and SCAR/WAVE, are involved in membrane-cytoskeletal interactions important for processes including membrane/vesicle trafficking, morphogenesis, angiogenesis, inflammatory immune response, and when mis-regulated, in pathogen infection, bleeding/bruising, immune deficiency and cancer metastasis. We have recently identified a third subfamily of WAS family proteins, designated WASH, that is conserved from Entamoeba to humans. The long-term goal of this proposal is to delineate both the cytoplasmic and nuclear function(s) of WASH and the developmental consequences of these processes going awry. The specific aims of this proposal are 1) to determine the role(s) of WASH in the regulation of actin and microtubule cytoskeletal coordination and cytoskeletal-membrane crosstalk using genetic, developmental, molecular/biochemical, and cell biological approaches; 2) to delineate the mechanisms of WASH function in hemocyte developmental and chemotactic migrations; and 3) to investigate the effect of WASH on nuclear architecture and organization using a combination of comparative bioinformatic, cell biological, and high-resolution microscopic approaches. The wealth of techniques, sophisticated live imaging, and reagents available in Drosophila make it an excellent, genetically manipulable, organism for studying the functions of WASH in vivo. Results obtained from these projects are expected to have wide implications as WASH is conserved throughout organisms. WASH will also serve as a reference protein for revealing general organizational principles and/or mechanisms for the roles of other actin-binding and cytoplasmic (cytoskeletal) proteins/families and will provide new insight into mechanisms controlling universal molecular and cell biological events both in and out of the nucleus. The information gathered in these projects will be important for understanding how WASH functions to control key cellular processes in normal development or when mis-regulated in disease states, and in the longer term, for the potential development of novel anti- disease drugs and/or therapies, or to enhance the effectiveness of existing treatments.
期刊论文(3)
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会议论文
DOI: 10.1091/mbc.e14-08-1266
发表时间: 2015-05-01
期刊: Molecular biology of the cell
影响因子: 3.3
作者: [Verboon JM, Rahe TK, Rodriguez-Mesa E, Parkhurst SM]
通讯作者: Parkhurst SM
Wiskott-Aldrich syndrome proteins in the nucleus: aWASH with possibilities.
细胞核中的 Wiskott-Aldrich 综合征蛋白:aWASH 的可能性。
DOI: 10.1080/19491034.2015.1086051
发表时间: 2015
期刊: Nucleus (Austin, Tex.)
影响因子: --
作者: [Verboon,JeffreyM, Sugumar,Bina, Parkhurst,SusanM]
通讯作者: Parkhurst,SusanM
Cellular mechanisms of nucleocytoplasmic export through Nuclear Envelope Budding
  • 批准号:
    10541746
  • 项目类别:
  • 资助金额:
    $8.55万
  • 财政年份:
    2021
  • 负责人:
    SUSAN M PARKHURST
  • 依托单位:
Cellular mechanisms of nucleocytoplasmic export through Nuclear Envelope Budding
  • 批准号:
    10642008
  • 项目类别:
  • 资助金额:
    $17.74万
  • 财政年份:
    2021
  • 负责人:
    SUSAN M PARKHURST
  • 依托单位:
Cellular mechanisms of nucleocytoplasmic export through Nuclear Envelope Budding
  • 批准号:
    10655419
  • 项目类别:
  • 资助金额:
    $38.66万
  • 财政年份:
    2021
  • 负责人:
    SUSAN M PARKHURST
  • 依托单位:
Cellular mechanisms of nucleocytoplasmic export through Nuclear Envelope Budding
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