Maternal-effect selfish element as gene drive for Anopheles mosquitoes
Maternal-effect selfish element as gene drive for Anopheles mosquitoes
批准号:
8272606
负责人:
Zhijian Jake Tu
金额:
$37.94万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-01 至 2015-05-31
关键词:
AllelesAnopheles GenusAntidotesAsiaAttentionBiochemistryBiteCandidate Disease GeneCharacteristicsChromosomesCommunicable DiseasesComplementary DNACulicidaeDNA Transposable ElementsDevelopmentDiagnosisDiseaseDrosophila genusDrug ControlsDrug resistanceElementsEmbryoEmbryonic DevelopmentEnsureEssential GenesExposure toFemaleFlourFrequenciesFutureGene Expression ProfileGene TargetingGenerationsGenesGeneticGenetic TranscriptionGenomeGenomicsGenotypeHomingHumanIndiumIndividualInheritedInsecticidesLaboratoriesLinkMalariaMeasuresMeiosisMethodsMicroRNAsModelingMolecular GeneticsMonitorMosquito-borne infectious diseaseOocytesOogenesisOutcomeOvaryPopulationPopulation ReplacementsPopulation StudyProcessReadingReagentRecording of previous eventsRefractoryRelative (related person)Reporter GenesReportingResearch DesignResource DevelopmentResourcesReverse Transcriptase Polymerase Chain ReactionRunningSamplingStagingSystemTargeted ToxinsTestingTimeTitaniaTitaniumToxinTranscriptTransgenesTransgenic OrganismsTriboliumVaccinesVariantVertebral columnVirginiaWolbachiacDNA Librarydesigndisorder controlendonucleaseexposed human populationgenetic effectorgenetic elementgenome sequencingnovel strategiesoffspringpathogenpromoterprototypepublic health relevancetoolvectorvector mosquito
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Anopheline mosquitoes are the primary vectors of malaria, one of the deadliest and most costly diseases in human history. Measures to control malaria are becoming less effective as both insecticide- and drug-resistance increases. It is clear that new approaches are urgently needed. A new strategy to control mosquito-borne diseases proposes to introduce so-called effector genes or refractory genes into the mosquito that will render the mosquitoes ineffective vectors for pathogens. Developing the means to drive effector genes in natural populations is an urgent priority. The long term objective of this study is to develop an efficient and safe gene drive mechanism that will enable genetic strategies for the control of mosquito-borne infectious diseases. Recently, Chen and colleagues (2007) reported the creation of a synthetic genetic element called Medea in Drosophila that successfully drove population replacement in laboratory. The Drosophila Medea element consists of two parts, a maternally expressed toxin in the form of artificial microRNAs that suppress Myd88, an essential gene for early embryonic development, and a zygotic antidote in the form of a variant of Myd88 that lacks the microRNA targets thus insensitive to the toxin. Building on our preliminary results, we will test the hypothesis that a synthetic Medea gene drive system can be developed in Anopheles stephensi. We will 1) determine the transcriptome profiles during oogenesis and early embryogenesis in An. stephensi; 2) select and test components of An. stephensi Medea; and 3) construct a complete An. stephensi Medea element and test for its maternal-effect selfish characteristics and gene drive ability.
PUBLIC HEALTH RELEVANCE: Anopheline mosquitoes are the primary vectors of malaria, which is one of the deadliest and most costly infectious diseases in human history. The long term objective of this study is to develop an efficient and safe gene drive mechanism that will enable genetic strategies for the control of mosquito-borne infectious diseases.
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