Elucidating the mechanisms of intrinsic stem cell resistance to virus infection
Elucidating the mechanisms of intrinsic stem cell resistance to virus infection
批准号:
10002173
负责人:
Xianfang Wu
金额:
$9.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-02 至 2021-03-31
关键词:
Advisory CommitteesAffectAntiviral resistanceAutomobile DrivingAwardBasic ScienceBindingBioinformaticsBiological AssayCell Differentiation processCellsChromatinClustered Regularly Interspaced Short Palindromic RepeatsCommunitiesComplementCounselingDataData SetDevelopmentDevelopment PlansEpigenetic ProcessEthicsEvolutionGene ExpressionGenesGenetic TranscriptionGoalsGrantGrowthHeartHematopoietic stem cellsHumanIRF1 geneImmunologyImmunoprecipitationIn VitroInfectionInterferonsKnock-outLaboratoriesMaintenanceMalignant NeoplasmsMediatingMentorsMethodologyMethodsMutagenesisNatural regenerationNew YorkOrganOrganismPathway interactionsPhasePhysiologicalPost-Translational Protein ProcessingProcessRegulationResearchResearch PersonnelResistanceResourcesRiceSignal TransductionTechniquesTestingTimeTissuesTrainingTransposaseUniversitiesViralVirusVirus DiseasesWorkWritingcareer developmentcell typecombatdifferential expressionepigenomeexperienceexperimental studyhuman embryonic stem cellhumanized mousein vivoinnovationknockout geneloss of functionmouse modelnew technologypathogenpermissivenesspromoterresponseskillsstemstem cell biologystem cell differentiationstem cellstissue repairtissue stem cellstranscription factortranscriptomevirologyvirus host interaction
中文摘要
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英文摘要
Project Summary
The primary research goal of this Pathway to Independence proposal is to understand and characterize the
mechanisms underlying intrinsic expression of interferon stimulated genes (ISGs) in stem cells. The
maintenance of healthy stem cells is essential for tissue repair within an organism. Unlike terminally
differentiated cells, however, stem cells do not produce the same robust interferon (IFN) response to combat
infection. The mechanisms by which stem cells potently block viral infection are still poorly understood. Our
recent discoveries demonstrate that stem cells have high basal levels of cell type-specific subsets of ISGs that
confer potent protection against a number of viruses. The mechanisms underlying this intrinsic ISG expression
remain elusive. To this end, in the mentored phase of this K99 award, the candidate will be trained in
epigenome techniques and bioinformatics to globally define chromatin accessibility associated with intrinsically
expressed ISGs in stem cells. As transcription factors (TFs) binding is often associated with these accessible
chromatin domains, the analysis of such coordination would allow him to identify TFs driving ISG expression in
stem cells. In addition, the candidate will receive training on CRISPR gene knockout screens, and further
define candidate TFs with these loss-of-function complementary experiments. Finally, the candidate will be
guided on detailed mechanistic characterization of newly identified TFs as well as IRF1, a TF specifically
regulates intrinsic ISG expression in hematopoietic stem cells. Additional components of the candidate's
comprehensive career development plan are courses and seminars in ethics and grant writing. The training
phase will be carried out in the laboratory of Dr. Charles Rice at The Rockefeller University (RU), one of the
world's leading laboratories in virology and immunology research. In addition to the significant resources and
basic science expertise in this laboratory, the candidate will also benefit from RU's vibrant research
community. A critical component of career development will be the close counsel of a highly experienced
Advisory Committee, composed of Dr. Charles Rice, Dr. C. David Allis, and Dr. Robert Roeder (all RU), and
Dr. David Levy (New York University). The innovative skills and comprehensive datasets obtained in the K99
training phase will set the stage for detailed understanding of the transcriptional networks that regulate intrinsic
ISG expression, and more importantly, antiviral resistance in stem cells. This will be key to succeed as a young
independent investigator in this highly competitive field of research. In all, the training will fulfill both the
candidate's short-term goals of adding new technologies, skills, and experience to his portfolio, and his long-
term goals, to become an independent investigator with a research focus on understanding important
processes at the heart of host-virus interactions. This study will have important implications for our
understanding of stem cell biology, primordial aspects in development and cancer, and the evolution of
vertebrate pathogen defense.
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海外基金