DNA-PKcs Phosphorylation on Hematopoietic Stem Cells Genome Maintenance
DNA-PKcs Phosphorylation on Hematopoietic Stem Cells Genome Maintenance
批准号:
8446279
负责人:
Benjamin Ping-Chi Chen
金额:
$31.01万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-04-01 至 2017-03-31
关键词:
AblationAdultAlanineApoptosisApoptoticAttenuatedBindingBiological PreservationBone Marrow TransplantationCatalytic DomainCell DeathCellsComplexDNADNA BindingDNA Double Strand BreakDNA RepairDNA-PKcsDNA-dependent protein kinaseDevelopmentDiseaseDouble Strand Break RepairDyskeratosis CongenitaEmbryoEukaryotaEventFailureFunctional disorderG22P1 geneGenesGenomeGenome StabilityGenomic InstabilityGenotoxic StressHematologic NeoplasmsHematopoieticHematopoietic stem cellsHeterogeneous-Nuclear RibonucleoproteinsHomeostasisHumanHyperpigmentationHypersensitivityInvadedInvestigationIonizing radiationKnock-outKnockout MiceLeadLengthLifeMaintenanceMalignant NeoplasmsMediatingMetabolismMusMutationNon-Hematologic MalignancyNonhomologous DNA End JoiningPancytopeniaPathway interactionsPatientsPhosphorylationProductionProliferatingProteinsSkinStaining methodStainsStressStretchingStructureSyndromeTelomerase RNA ComponentTelomere Length MaintenanceTelomere MaintenanceWorkXRCC5 genebasecarcinogenesishnRNP A1homologous recombinationintestinal cryptmouse modelnull mutationresponsetelomere
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The DNA dependent protein kinase catalytic subunit (DNA-PKcs) and its DNA-binding partner the Ku70/80 heterodimer are the key components of the non-homologous end-joining (NHEJ) pathway. In response to DNA double-strand breaks (DSBs), DNA-PKcs is rapidly phosphorylated at the T2609 cluster, an event critical for DSB repair. DNA-PKcs "3A" knockin mice, in which phosphorylation at three residues in the mouse T2605 cluster (human T2609 cluster) are ablated via alanine substitution, die prematurely due to congenital bone marrow failure. Loss of hematopoietic stem cells (HSCs) in DNA-PKcs3A/3A mice is caused by elevated genotoxic stress as evidenced by increased intestinal crypt apoptosis and skin hyperpigmentation. Although these mice die prematurely, they can be rescued with bone marrow transplantation. BMT-rescued DNA- PKcs3A/3A mice are prone to develop both hematologic and non-hematologic cancers. HSC loss and hyperpigmented skin are the main features found in human dyskeratosis congenita (DC) syndrome and in mice double knockout of protection of telomeres 1b (POT1b) and telomerase RNA (mTR) genes. In addition, DC patients are also prone to cancer development. DC patients and POT1b/mTR DKO mice are unable to properly maintain the telomeres. Based on these findings, we hypothesize that the expression of the DNA-PKcs3A protein will lead to telomere dysregulation, genome instability, and carcinogenesis. We propose in this project to further elucidate the mechanism by which DNA-PKcs T2609 cluster phosphorylation impacts HSC homeostasis and telomere maintenance. Our specific aims are: 1. To investigate how DNA-PKcs T2609 cluster phosphorylation and the DNA-PKcs interaction with the Ku70/80 heterodimer impacts hematopoietic stem cell homeostasis. 2. To investigate the effect of DNA-PKcs T2609 cluster phosphorylation on telomere maintenance. 3. To determine the effect of DNA-PKcs T2609 cluster phosphorylation on the production and protection of telomeric 3' overhangs.
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会议论文
DNA-PKcs and PIDD interaction in DNA damage response
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批准号:10228547
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项目类别:
-
资助金额:$37.06万
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财政年份:2019
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负责人:Benjamin Ping-Chi Chen
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依托单位:
DNA-PKcs and PIDD interaction in DNA damage response
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批准号:9920680
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项目类别:
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资助金额:$37.06万
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财政年份:2019
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负责人:Benjamin Ping-Chi Chen
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依托单位:
DNA-PKcs Phosphorylation on Hematopoietic Stem Cells Genome Maintenance
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批准号:8633438
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项目类别:
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资助金额:$32.0万
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财政年份:2012
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负责人:Benjamin Ping-Chi Chen
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依托单位:
DNA-PKcs Phosphorylation on Hematopoietic Stem Cells Genome Maintenance
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批准号:8275973
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项目类别:
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资助金额:$32.95万
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财政年份:2012
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负责人:Benjamin Ping-Chi Chen
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依托单位:
Translational Control of Radiation-Induced Apoptosis
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批准号:7059786
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项目类别:
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资助金额:$0.47万
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财政年份:2009
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负责人:Benjamin Ping-Chi Chen
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依托单位:
海外基金