FANCD2 interaction with mismatch repair proteins and MCM2-7
FANCD2 与错配修复蛋白和 MCM2-7 的相互作用
基本信息
- 批准号:8616392
- 负责人:
- 金额:$ 48.66万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2000
- 资助国家:美国
- 起止时间:2000-09-10 至 2016-01-31
- 项目状态:已结题
- 来源:
- 关键词:AffectBRCA1 geneBindingBiochemicalBiochemical PathwayBiochemistryBiologyCancer EtiologyCancer Prevention InterventionCellsChromatinComplexDNADNA Crosslinking AgentDNA DamageDNA RepairDataDefectDissectionEventFANCD2 proteinFanconi anemia proteinFanconi&aposs AnemiaGenetic RecombinationGenomic DNAGenomic InstabilityGoalsHematological DiseaseHematopoiesisHematopoietic NeoplasmsHereditary DiseaseHypersensitivityLaboratoriesLeadMCM2 geneMLH1 geneMSH2 geneMalignant NeoplasmsMapsMismatch RepairModelingNormal CellPathway interactionsPediatric Hematology/OncologyPhenotypePhosphorylationPhosphorylation SitePredispositionProcessProteinsResearchResistanceS PhaseSignal TransductionTestingWorkcancer therapyhelicasehomologous recombinationhuman MCM2 proteininsightleukemiamutantpreventprotein functionpublic health relevancerepairedresponse
项目摘要
DESCRIPTION (provided by applicant): The Fanconi anemia (FA) phenotype on a cellular level is marked by genomic instability and hypersensitivity to DNA damage. FA proteins participate in complexes that juxtapose the FA pathway with other more defined pathways involved in cellular response to DNA damage, such as ATR, BRCA1, and RAD51. Recent work has served to shift focus of FA biology and the normal functions of these proteins onto homologous recombination pathways. However, much remains to be ascertained in normal FA biochemistry or about the manner in which FA proteins contribute to hematopoiesis and leukemia, as the FA proteins contain few known functional motifs. Insight into the biochemical pathway of FA is important because this would lead to a mechanism whereby genomic instability occurs, which is a basic cause of cancer. This understanding makes possible interventions for cancer prevention as well as manipulation of genomic instability for cancer therapy. The long-term goal of my laboratory is to define mechanisms of genomic instability, using FA as a model, as well as to understand the normal function of FA proteins. The central hypothesis for the proposed research is that FANCD2 acts as a signal transduction protein to interact with downstream effectors such as the MSH2, the mismatch repair protein, and the MCM2-7 complex, which is critical for pre-origin loading of the replication machinery. Our work suggests that both these processes depend on upstream phosphorylation events. To test our central hypothesis and carry out this application, we will pursue the following specific aims: Aim #1: Determine the functional consequence of FANCD2-MSH2 interaction The working hypothesis for Aim #1 is that FANCD2-MSH2 interaction is important for the normal DNA damage response. Our data have shown that not only does MSH2 knockdown result in DNA damage hypersensitivity but also double knockdown of both FANCD2 and MSH2 contradictorily results in cellular resistance. Aim #2: Determine the functional consequence of FANCD2-MLH1 interaction The working hypothesis for Aim #2 is that FANCD2-MLH1 interaction is important for the normal DNA damage response. We show that MLH1 loss does not affect FANCD2 monoubiquitylation but does prevent the propagation of signal to chromatin and subsequent increased sensitivity to DNA crosslinkers. Aim #3: Demonstrate the functional consequence of FANCD2-MCM2-7 interaction The working hypothesis for Aim #2 is that FANCD2-MCM2-7 interaction regulates the assembly of the replication complex at the origin by responding to DNA damage during S phase. Our data indicate that binding to a subset of the MCM subunits results in inhibition of replication complex assembly. Understanding the FA pathway will further elaborate a key repair pathway as well as lend insight into avenues of targeting cancer therapy.
描述(由申请人提供):细胞水平上的范可尼贫血(FA)表型以基因组不稳定性和对DNA损伤的超敏反应为特征。FA蛋白参与复合物,该复合物将FA途径与参与对DNA损伤的细胞反应的其他更明确的途径(例如ATR、BRCA 1和RAD 51)并列。最近的工作已经将FA生物学的焦点和这些蛋白质的正常功能转移到同源重组途径上。然而,在正常的FA生物化学或FA蛋白有助于造血和白血病的方式仍有待确定,因为FA蛋白含有很少的已知功能基序。深入了解FA的生化途径是重要的,因为这将导致基因组不稳定性发生的机制,这是癌症的基本原因。这种理解使得癌症预防的干预以及癌症治疗中基因组不稳定性的操纵成为可能。我实验室的长期目标是以FA为模型,确定基因组不稳定性的机制,并了解FA蛋白的正常功能。这项研究的中心假设是,FANCD 2作为一种信号转导蛋白与下游效应物相互作用,如MSH 2、错配修复蛋白和MCM 2 -7复合物,这对复制机制的起始前加载至关重要。我们的工作表明,这两个过程依赖于上游磷酸化事件。为了检验我们的中心假设并实现这一应用,我们将追求以下具体目标:目标#1:确定FANCD 2-MSH 2相互作用的功能后果目标#1的工作假设是FANCD 2-MSH 2相互作用对正常DNA损伤反应是重要的。我们的数据表明,不仅MSH 2敲低导致DNA损伤超敏反应,而且FANCD 2和MSH 2的双重敲低矛盾地导致细胞抗性。目标二:目的#2的工作假设是FANCD 2-MLH 1相互作用对于正常的DNA损伤应答是重要的。我们表明,MLH 1的损失不影响FANCD 2单泛素化,但确实阻止了信号传播到染色质和随后的DNA交联剂的敏感性增加。目标3:证明FANCD 2-MCM 2 -7相互作用的功能后果目标#2的工作假设是FANCD 2-MCM 2 -7相互作用通过响应S期期间的DNA损伤来调节复制复合物在起点的组装。我们的数据表明,结合到一个子集的MCM亚基的结果在复制复合物组装的抑制。了解FA途径将进一步阐述关键的修复途径,并深入了解靶向癌症治疗的途径。
项目成果
期刊论文数量(8)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Fanconi anemia complementation group FANCD2 protein serine 331 phosphorylation is important for fanconi anemia pathway function and BRCA2 interaction.
- DOI:10.1158/0008-5472.can-09-2312
- 发表时间:2009-11-15
- 期刊:
- 影响因子:11.2
- 作者:Zhi G;Wilson JB;Chen X;Krause DS;Xiao Y;Jones NJ;Kupfer GM
- 通讯作者:Kupfer GM
Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance.
BRCA2/D1-D2-G-X3 复合物的组装、FANCD2 单泛素化和腐草霉素抗性需要 FANCG 的几个四肽重复 (TPR) 基序。
- DOI:10.1016/j.mrfmmm.2010.04.003
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:Wilson,JamesB;Blom,Eric;Cunningham,Ryan;Xiao,Yuxuan;Kupfer,GaryM;Jones,NigelJ
- 通讯作者:Jones,NigelJ
Fanconi anemia: a signal transduction and DNA repair pathway.
范可尼贫血:信号转导和 DNA 修复途径。
- DOI:
- 发表时间:2013
- 期刊:
- 影响因子:0
- 作者:Kupfer,GaryM
- 通讯作者:Kupfer,GaryM
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Gary M. Kupfer其他文献
Complex Formation between FANCD2 and the Splicing Factor SRSF1 Helps Prevent R-Loop Accumulation through mRNA Export Regulation
- DOI:
10.1182/blood-2022-166798 - 发表时间:
2022-11-15 - 期刊:
- 影响因子:
- 作者:
Anne Olazabal Herrero;Fengshan Liang;Arijit Dutta;Yuxin Huang;Zhuobin Liang;Abhishek K Gupta;Li Lan;Manoj M Pillai;Patrick Sung;Gary M. Kupfer - 通讯作者:
Gary M. Kupfer
The Fanconi anaemia proteins, FAA and FAC interact to form a nuclear complex
范可尼贫血蛋白(FAA)和 FAC 相互作用形成一个核复合物。
- DOI:
10.1038/ng1297-487 - 发表时间:
1997-12-01 - 期刊:
- 影响因子:29.000
- 作者:
Gary M. Kupfer;Dieter Näf;Ahmed Suliman;Michael Pulsipher;Alan D. D'Andrea - 通讯作者:
Alan D. D'Andrea
A ROS-mediated oxidation-O-GlcNAcylation cascade governs ferroptosis
一个由 ROS 介导的氧化-O-GlcNAcylation 级联调控铁死亡
- DOI:
10.1038/s41556-025-01722-w - 发表时间:
2025-07-18 - 期刊:
- 影响因子:19.100
- 作者:
Hemeng Zhang;Jialin Ma;Chunyan Hou;Xuehui Luo;Shiya Zhu;Yihan Peng;Changmin Peng;Ping Li;Heng Meng;Yuqi Xia;Zhinuo Jiang;Susree Modepalli;Anju Duttargi;Gary M. Kupfer;Mengjiao Cai;Heng Zhang;Junfeng Ma;Juanjuan Li;Suxia Han;Huadong Pei - 通讯作者:
Huadong Pei
Gary M. Kupfer的其他文献
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{{ truncateString('Gary M. Kupfer', 18)}}的其他基金
Mechanistic Dissection of the Falconi Anemia Pathway of DNA Damage Response and Repair
法尔科尼贫血 DNA 损伤反应和修复途径的机制剖析
- 批准号:
9899099 - 财政年份:2019
- 资助金额:
$ 48.66万 - 项目类别:
Mechanistic Dissection of the BRCA1-SETX-dependent Pathway of R-loop Avoidance and Genome Maintenance
R 环避免和基因组维护的 BRCA1-SETX 依赖性途径的机制剖析
- 批准号:
10537108 - 财政年份:2013
- 资助金额:
$ 48.66万 - 项目类别:
Mechanistic Dissection of the Fanconi Anemia Pathway of DNA Damage Response and R
DNA 损伤反应和 R 范可尼贫血途径的机制剖析
- 批准号:
8505689 - 财政年份:2013
- 资助金额:
$ 48.66万 - 项目类别:
Mechanistic Dissection of the Fanconi Anemia Pathway of DNA Damage Response and R
DNA 损伤反应和 R 范可尼贫血途径的机制剖析
- 批准号:
8641673 - 财政年份:2013
- 资助金额:
$ 48.66万 - 项目类别:
Mechanistic Dissection of the BRCA1-SETX-dependent Pathway of R-loop Avoidance and Genome Maintenance
R 环避免和基因组维护的 BRCA1-SETX 依赖性途径的机制剖析
- 批准号:
10641022 - 财政年份:2013
- 资助金额:
$ 48.66万 - 项目类别:
Mechanistic Dissection of the Fanconi Anemia Pathway of DNA Damage Response and R
DNA 损伤反应和 R 范可尼贫血途径的机制剖析
- 批准号:
8826073 - 财政年份:2013
- 资助金额:
$ 48.66万 - 项目类别:
HTLV I Tax1 protein chemosensitization of p53 mutant tumors
HTLV I Tax1 蛋白对 p53 突变肿瘤的化疗增敏
- 批准号:
8053781 - 财政年份:2010
- 资助金额:
$ 48.66万 - 项目类别:
HTLV I Tax1 protein chemosensitization of p53 mutant tumors
HTLV I Tax1 蛋白对 p53 突变肿瘤的化疗增敏
- 批准号:
7872281 - 财政年份:2010
- 资助金额:
$ 48.66万 - 项目类别:
The Fanconi Anemia Core and D2 Complexes
Fanconi 贫血核心和 D2 复合物
- 批准号:
7440298 - 财政年份:2000
- 资助金额:
$ 48.66万 - 项目类别:
FANCD2 interaction with mismatch repair proteins and MCM2-7
FANCD2 与错配修复蛋白和 MCM2-7 的相互作用
- 批准号:
8231274 - 财政年份:2000
- 资助金额:
$ 48.66万 - 项目类别:
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