Evolution of Meiotic Mechanisms in Divergent Cytological Environments
Evolution of Meiotic Mechanisms in Divergent Cytological Environments
批准号:
8457163
负责人:
Kevin Wright
金额:
$5.22万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-02-01 至 2016-01-31
关键词:
AddressAffectAllelesAnimal ModelArabidopsisBackcrossingsBiological ProcessCatalogingCatalogsCellsChromatin StructureChromosome MappingChromosome PairingChromosome SegregationChromosomesDataDevelopmentDiploidyDiseaseDown SyndromeElementsEnsureEnvironmentEventEvolutionFertilityFluorescent in Situ HybridizationFrequenciesGenerationsGenesGenetic Crossing OverGenetic TransformationGenomeGenomicsGenotypeGerm CellsHomologous GeneInfertilityInvestigationLaboratoriesLaboratory ResearchLeadMapsMeasuresMeiosisMolecularMolecular GeneticsMolecular ProfilingMutationNatureOptic ChiasmOrganismPolyploidyProcessProphaseProteinsRecurrenceRibosomal DNASpontaneous abortionSterilitySystemSystems DevelopmentTestingTransgenic OrganismsVariantbaseexperiencegenome sequencinginterestnovelpressureprotein functionpublic health relevanceresearch studyresponsesegregationstructural genomics
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Meiosis is a fundamental process for all sexual reproducing organisms. Problems in this process can lead to chromosome mis-segregation, which can result in sterility, lethality, and diseases such as Down's syndrome. Many proteins and elements of meiosis are evolutionarily conserved, there is species level variation in the precise meiotic mechanisms, but there is remarkably little data on how these different mechanisms or the associated proteins have evolved. I propose to address the question of how a novel meiotic process and associated proteins evolve by studying cytological and functional molecular genetic differences between closely related diploid and autotetraploid Arabidopsis arenosa. Polyploidy is an ideal system to study this question, because there is strong selective pressure on the meiosis machinery to ensure proper pairing, crossing- over, and segregation in an environment with double the number of homologous chromosomes. To catalogue the differences between these environments, I propose to conduct a detailed cytological investigation of diploid, natural autotetraploid, and synthetic tetraploid lines. I will also investigate the function of meiosis related proteins with strong signatures of selection in the tetraploid lineage through transgenic analysis. In a complimentary experiment, I will conduct an artificial selection experiment on gamete viability in the synthetic autotetraploid and genetically
map loci that ensure proper meiosis in the tetraploid.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Transcriptional control of retinal neuron specification and maturation.
-
批准号:10093946
-
项目类别:
-
资助金额:$38.5万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
Transcriptional control of retinal neuron specification and maturation.
-
批准号:10600979
-
项目类别:
-
资助金额:$38.5万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
Supplement to: Transcription control of retinal neuron specification and maturation
-
批准号:10429697
-
项目类别:
-
资助金额:$7.32万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
Transcriptional control of retinal neuron specification and maturation.
-
批准号:10574464
-
项目类别:
-
资助金额:$7.32万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
Transcriptional control of retinal neuron specification and maturation.
-
批准号:10318626
-
项目类别:
-
资助金额:$37.35万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
Transcriptional control of retinal neuron specification and maturation.
-
批准号:10846942
-
项目类别:
-
资助金额:$7.32万
-
财政年份:2021
-
负责人:Kevin Wright
-
依托单位:
The role of dystroglycan in neural circuit development.
-
批准号:9308019
-
项目类别:
-
资助金额:$33.69万
-
财政年份:2016
-
负责人:Kevin Wright
-
依托单位:
The role of dystroglycan in neural circuit development.
-
批准号:9979988
-
项目类别:
-
资助金额:$33.69万
-
财政年份:2016
-
负责人:Kevin Wright
-
依托单位:
海外基金