The Role of Stu1 in Mitotic Spindle Stability
Stu1 在有丝分裂纺锤体稳定性中的作用
基本信息
- 批准号:7545477
- 负责人:
- 金额:$ 2.86万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-01-01 至 2009-08-15
- 项目状态:已结题
- 来源:
- 关键词:Affinity ChromatographyAneuploid CellsAntibodiesBiochemicalBiochemistryCell CycleCell divisionComplexEukaryotaGeneticGenetic MaterialsGenetic ScreeningHereditary DiseaseHomologous GeneImmunofluorescence ImmunologicIn VitroKinetochoresLeadMaintenanceMass Spectrum AnalysisMicrotubule-Associated ProteinsMicrotubulesMitotic spindleModelingMotorOpen Reading FramesProtein FamilyProteinsRoleSaccharomyces cerevisiae ProteinsStructureSystemTestingXenopusXenopus ProteinsXenopus laevisYeast Model SystemYeastscDNA Librarycancer geneticsegggenetic analysisinsightnovelsegregation
项目摘要
DESCRIPTION (provided by applicant): Proper segregation of genetic material during cell division is critical and depends on the formation and stability of the bipolar mitotic spindle composed of microtubules and associated proteins. Aneuploid cells resulting from mis-segregation suffer detrimental effects and reduced viability as observed in cancers and genetic diseases. The Saccharomyces cerevisiae protein Stulp interacts with microtubules, localizes to the mitotic spindle midzone region, and is essential for proper spindle structure and viability. However, proteins that interact with Stu1 and the role of Stu1p in formation and maintenance of the mitotic spindle is not understood. Identification of Stu1 associating proteins using Tandem Affinity Purification (TAP) and mass spectroscopy will aid in understanding the context of Stu1 in the spindle: Yeast is a valuable genetic system, but in depth biochemistry is limited. Xenopus laevis egg extracts are a powerful in vitro system for studying spindle formation and microtubule dynamics. Immunolocalization and immunodepletion of extracts using antibodies against a Xenopus protein identified from cDNA libraries encoding a Stu1 homologue will allow analysis of this class of proteins in bipolar spindle formation and microtubule dynamics.
描述(由申请人提供):细胞分裂过程中遗传物质的适当分离是至关重要的,它取决于由微管和相关蛋白组成的双极有丝分裂纺锤体的形成和稳定性。如在癌症和遗传疾病中所观察到的那样,由错误分离产生的非整倍体细胞受到有害影响并降低活力。酿酒酵母蛋白Stulp与微管相互作用,定位于有丝分裂纺锤体中部区域,对纺锤体的正常结构和生存能力至关重要。然而,与Stu1相互作用的蛋白质以及Stu1在有丝分裂纺锤体形成和维持中的作用尚不清楚。使用串联亲和纯化(TAP)和质谱鉴定Stu1相关蛋白将有助于了解纺锤体中Stu1的背景:酵母是一个有价值的遗传系统,但深入的生物化学是有限的。非洲爪蟾卵提取物是研究纺锤体形成和微管动力学的一个强有力的体外系统。利用从编码Stu1同源基因的cDNA文库中鉴定出的针对非洲爪蟾蛋白的抗体进行免疫定位和免疫消耗,可以分析这类蛋白的双极纺锤体形成和微管动力学。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
IRENE Alexandra AMARO其他文献
IRENE Alexandra AMARO的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('IRENE Alexandra AMARO', 18)}}的其他基金
The Role of Stu1 in Mitotic Spindle Stability
Stu1 在有丝分裂纺锤体稳定性中的作用
- 批准号:
6965507 - 财政年份:2005
- 资助金额:
$ 2.86万 - 项目类别:
The Role of Stu1 in Mitotic Spindle Stability
Stu1 在有丝分裂纺锤体稳定性中的作用
- 批准号:
6892608 - 财政年份:2005
- 资助金额:
$ 2.86万 - 项目类别:
The Role of Stu1 in Mitotic Spindle Stability
Stu1 在有丝分裂纺锤体稳定性中的作用
- 批准号:
7254246 - 财政年份:2005
- 资助金额:
$ 2.86万 - 项目类别:
The Role of Stu1 in Mitotic Spindle Stability
Stu1 在有丝分裂纺锤体稳定性中的作用
- 批准号:
7336304 - 财政年份:2005
- 资助金额:
$ 2.86万 - 项目类别:
相似海外基金
Biological mechanisms that eliminate aneuploid cells from a mosaic conceptus in the mouse model system
从小鼠模型系统中的嵌合体概念中消除非整倍体细胞的生物学机制
- 批准号:
10379454 - 财政年份:2021
- 资助金额:
$ 2.86万 - 项目类别:
Identifying mechanisms that detect and eliminate aneuploid cells
识别检测和消除非整倍体细胞的机制
- 批准号:
10320458 - 财政年份:2021
- 资助金额:
$ 2.86万 - 项目类别:
Biological mechanisms that eliminate aneuploid cells from a mosaic conceptus in the mouse model system
从小鼠模型系统中的嵌合体概念中消除非整倍体细胞的生物学机制
- 批准号:
10557129 - 财政年份:2021
- 资助金额:
$ 2.86万 - 项目类别:
Metabolic changes in the trophectoderm induce the selective elimination of aneuploid cells by apoptosis
滋养外胚层的代谢变化诱导细胞凋亡选择性消除非整倍体细胞
- 批准号:
9924594 - 财政年份:2019
- 资助金额:
$ 2.86万 - 项目类别:
Role of de Novo Synthesis of Sphingolipids in Aneuploid Cells
鞘脂从头合成在非整倍体细胞中的作用
- 批准号:
9238913 - 财政年份:2017
- 资助金额:
$ 2.86万 - 项目类别:
Role of de Novo Synthesis of Sphingolipids in Aneuploid Cells
鞘脂从头合成在非整倍体细胞中的作用
- 批准号:
10084296 - 财政年份:2017
- 资助金额:
$ 2.86万 - 项目类别:
The fate of aneuploid cells
非整倍体细胞的命运
- 批准号:
15H02398 - 财政年份:2015
- 资助金额:
$ 2.86万 - 项目类别:
Grant-in-Aid for Scientific Research (A)














{{item.name}}会员




