Cellular Functions of the Tumor Suppressor APC
Cellular Functions of the Tumor Suppressor APC
批准号:
8054741
负责人:
BROOKE M MCCARTNEY
金额:
$24.43万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-04-15 至 2012-03-31
关键词:
APC2 geneActinsAdenomatous Polyposis ColiAdenomatous Polyposis Coli ProteinAffectAttentionBehaviorBindingBiochemicalBiochemical GeneticsBiological AssayCOX7A2L ProteinCadherinsCell CycleCell physiologyCentrosomeColon CarcinomaComplexCultured CellsCytoskeletal ModelingCytoskeletonDNA Sequence RearrangementDataDevelopmentDrosophila genusEmbryoFamilyFamily DasypodidaeFilamentFunctional disorderGoalsHomologous GeneImaging TechniquesInheritedLifeMalignant NeoplasmsMicrofilamentsMicrotubule StabilizationMicrotubulesModelingMusMutationNormal CellPathway interactionsPhosphorylationPhosphotransferasesPlayPlus End of the MicrotubuleProcessProtein DynamicsProteinsRegulationResearch PersonnelRoleSignal TransductionSignal Transduction PathwayStructureSystemTertiary Protein StructureTestingTumor Suppressor Proteinsflygenetic regulatory proteinin vitro Assayin vivorho
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The colon cancer tumor suppressor Adenomatous polyposis coli (APC) acts as an essential negative regulator of the Wnt signal transduction pathway and also has fundamental roles in the regulation of the actin and microtubule cytoskeletons. The precise mechanisms by which APC proteins influence the cytoskeleton have not been defined and may contribute to the development of colon cancer. We have developed an in vivo system in which to study the cytoskeletal functions of Drosophila APC2 using the Drosophila syncytial embryo as a model for cytoskeletal organization. Here, dynamic rearrangements of cortical actin during the cell cycle are orchestrated by a number of known actin regulatory proteins and by interactions with centrosomes and microtubules. We have previously shown that Drosophila APC2 plays a role in organization of the syncytial cytoskeleton in a complex including the Drosophila B-catenin homolog, Armadillo, and a-catenin. Our continued study of APC2 in this system revealed that APC2 functions to organize actin structures in the syncytial embryo and that this function is carried out in part with a Drosophila formin homology domain protein Diaphanous. The overall goals of this project include defining the molecular interactions of APC2 within the Armadillo-a-catenin complex and the Diaphanous complex and to understand in detail how these complexes are functioning to organize the actin cytoskeleton using biochemical assays, live imaging techniques, analysis of actin and microtubule organization and behavior, and identification of other proteins partners and regulators. These findings will contribute not only to our appreciation of normal cell processes, but also to our understanding of cellular dysfunction and cancer.
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The two SAMP repeats and their phosphorylation state in Drosophila Adenomatous polyposis coli-2 play mechanistically distinct roles in negatively regulating Wnt signaling.
果蝇腺瘤性息肉病 coli-2 中的两个 SAMP 重复序列及其磷酸化状态在负调节 Wnt 信号传导中发挥着机制上不同的作用。
DOI:
10.1091/mbc.e15-07-0515
发表时间:
2015
期刊:
Molecular biology of the cell
影响因子:
3.3
作者:
[Kunttas-Tatli,Ezgi, VonKleeck,RyanA, Greaves,BradfordD, Vinson,David, Roberts,DavidM, McCartney,BrookeM]
通讯作者:
McCartney,BrookeM
DOI:
10.1002/dvdy.22076
发表时间:
2009-10
期刊:
DEVELOPMENTAL DYNAMICS
影响因子:
2.5
作者:
[Webb, Rebecca L., Rozov, Orr, Watkins, Simon C., McCartney, Brooke M.]
通讯作者:
McCartney, Brooke M.
Apical constriction and invagination downstream of the canonical Wnt signaling pathway require Rho1 and Myosin II.
经典 Wnt 信号通路下游的顶端收缩和内陷需要 Rho1 和肌球蛋白 II。
DOI:
10.1016/j.ydbio.2010.01.021
发表时间:
2010
期刊:
Developmental biology
影响因子:
2.7
作者:
[Zimmerman,SandraG, Thorpe,LaurenM, Medrano,VilmaR, Mallozzi,CarolynA, McCartney,BrookeM]
通讯作者:
McCartney,BrookeM
Cortical localization of APC2 plays a role in actin organization but not in Wnt signaling in Drosophila.
APC2 的皮质定位在肌动蛋白组织中发挥作用,但在果蝇的 Wnt 信号传导中不起作用。
DOI:
10.1242/jcs.073916
发表时间:
2011
期刊:
Journal of cell science
影响因子:
4
作者:
[Zhou,Meng-Ning, Kunttas-Tatli,Ezgi, Zimmerman,Sandra, Zhouzheng,Fangyuan, McCartney,BrookeM]
通讯作者:
McCartney,BrookeM
DOI:
10.1091/mbc.e14-04-0885
发表时间:
2014-11-01
期刊:
Molecular biology of the cell
影响因子:
3.3
作者:
[Kunttas-Tatli E, Roberts DM, McCartney BM]
通讯作者:
McCartney BM
共 6 条
ACTIN CABLE FORMATION COORDINATED BY APC, FORMINS AND MICROTUBULES IN ANIMAL DEVELOPMENT
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批准号:9923672
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项目类别:
-
资助金额:$29.17万
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财政年份:2017
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负责人:BROOKE M MCCARTNEY
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依托单位:
Cellular Functions of the Tumor Suppressor APC
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批准号:7788098
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项目类别:
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资助金额:$24.74万
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财政年份:2007
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负责人:BROOKE M MCCARTNEY
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依托单位:
Cellular Functions of the Tumor Suppressor APC
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批准号:7406088
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项目类别:
-
资助金额:$25.11万
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财政年份:2007
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负责人:BROOKE M MCCARTNEY
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依托单位:
Cellular Functions of the Tumor Suppressor APC
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批准号:7260782
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项目类别:
-
资助金额:$25.16万
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财政年份:2007
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负责人:BROOKE M MCCARTNEY
-
依托单位:
Cellular Functions of the Tumor Suppressor APC
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批准号:7596849
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项目类别:
-
资助金额:$25.05万
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财政年份:2007
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负责人:BROOKE M MCCARTNEY
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依托单位:
NORMAL CELLULAR FUNCTIONS OF DROSOPHILA APC
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批准号:6322315
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项目类别:
-
资助金额:$3.58万
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财政年份:2000
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负责人:BROOKE M MCCARTNEY
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依托单位:
NORMAL CELLULAR FUNCTIONS OF DROSOPHILA APC
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批准号:2710681
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项目类别:
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资助金额:$2.62万
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财政年份:1999
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负责人:BROOKE M MCCARTNEY
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依托单位:
NORMAL CELLULAR FUNCTIONS OF DROSOPHILA APC
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批准号:6087562
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项目类别:
-
资助金额:$3.67万
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财政年份:1998
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负责人:BROOKE M MCCARTNEY
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依托单位:
海外基金