Comparative Genomics of Peroxisomal Lipid Metabolism
Comparative Genomics of Peroxisomal Lipid Metabolism
批准号:
7931167
负责人:
JOSEPH G HACIA
金额:
$23.23万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-03-31
关键词:
AcidsAffectAfricaAfricanAllelesAsiansBiochemicalBiological ModelsCardiovascular systemCatabolismCellsCellular biologyCercopithecidaeColobus GenusComplexConsumptionDietDietary FatsDiseaseEatingEnvironmentEnzymesEvolutionFatty AcidsFibroblastsFruitGene ExpressionGenesGeneticGenetic PolymorphismGenomicsGoalsGorilla gorillaHealthHomoHumanHuman GenomeIntakeLeftLipidsLiverMacaca mulattaMeasuresMeatMetabolicMetabolic PathwayMitochondriaMixed Function OxygenasesMorphologyNatural SelectionsNeuronsPan GenusPan paniscusPapio anubisPathway interactionsPatternPhenotypePhysiologicalPhytanic AcidPlasmalogensPoaceaePongidaePongo pygmaeusPrimatesRelative (related person)Research PersonnelRoleShapesTestingTheropithecus geladaVariantVery Long Chain Fatty Acidbasecomparativefunctional genomicshuman migrationlipid metabolismlong chain fatty acidmigrationnonhuman primateoxidationperoxisomephytanoyl-coenzyme Apressureresponsesample fixationskeletal
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Interactions between the human genome and the environment have shaped the evolution of complex human phenotypes. Since the emergence of the genus Homo, there have been many significant changes in the interactions of humans and their ancestors with their environments. One such interaction involves dramatic increases in meat consumption prior to migrations of modern humans out of Africa. We hypothesize that humans and their ancestors have undergone selection in lipid metabolism genes in response to dietary shifts. Based on the known physiological importance of these pathways, these selective changes could strongly influence complex human phenotypes involving the nervous and cardiovascular systems and the liver.
In this proposal, we will take comparative and functional genomics approaches to identify specific lipid metabolism genes and pathways undergoing selection in the human lineage. Here, we will compare and contrast quantitative differences in peroxisomal lipid metabolism in humans and closely related primate species that are primarily fruiteating, leaf-eating, grass-eating, or omnivorous. We will examine cellular differences in these metabolic pathways using fibroblasts, an established model system for peroxisomal lipid metabolism. In Specific Aim 1, we will take biochemical approaches to quantify the activities of these metabolic pathways in each species. We will focus on the catabolism of fatty acids abundant in meat-eating diets which we predict will show species-specific activities dependent upon diet. In Specific Aim 2, we will take cellular biology approaches to evaluate peroxisomal assembly and integrity in each species and correlate with their rates of lipid catabolism. In Specific Aim 3, we will take genomics approaches to evaluate the expression of peroxisomal genes and transcriptional responses to treatment with dietary lipids. In Specific Aim 4, we will take statistical genetics approaches to conduct detailed tests for selection in peroxisomal lipid metabolic genes in human and other primates. We will screen for selective sweeps that occurred prior to the migration of humans out of Africa that could mark the fixation of advantageous alleles in humans. Overall, we will conduct a detailed analysis of selective changes in human peroxisomal lipid metabolism using a variety of newly developed functional and comparative genomic approaches that could be applied towards other studies examining metabolic pathways relevant to human health and disease.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1186/1471-2350-13-72
发表时间:
2012-08-15
期刊:
BMC medical genetics
影响因子:
--
作者:
[Levesque S, Morin C, Guay SP, Villeneuve J, Marquis P, Yik WY, Jiralerspong S, Bouchard L, Steinberg S, Hacia JG, Dewar K, Braverman NE]
通讯作者:
Braverman NE
DOI:
10.1186/scrt130
发表时间:
2012-10-04
期刊:
Stem cell research & therapy
影响因子:
7.5
作者:
[Wang XM, Yik WY, Zhang P, Lu W, Dranchak PK, Shibata D, Steinberg SJ, Hacia JG]
通讯作者:
Hacia JG
DOI:
10.1186/s13104-015-1567-0
发表时间:
2015-10-16
期刊:
BMC research notes
影响因子:
1.8
作者:
[Ramaswamy K, Yik WY, Wang XM, Oliphant EN, Lu W, Shibata D, Ryder OA, Hacia JG]
通讯作者:
Hacia JG
Development of Targeted Therapies for Peroxisome Biogenesis Disorders: Current and future prospects
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批准号:9261342
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项目类别:
-
资助金额:$1.3万
-
财政年份:2016
-
负责人:JOSEPH G HACIA
-
依托单位:
Development of Targeted Therapies for Peroxisome Biogenesis Disorders: Current and future prospects
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批准号:9447324
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项目类别:
-
资助金额:$0.3万
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财政年份:2016
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负责人:JOSEPH G HACIA
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依托单位:
Development of Targeted Therapies for Peroxisome Biogenesis Disorders: Current and future prospects
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批准号:9440507
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项目类别:
-
资助金额:$1.0万
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财政年份:2016
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负责人:JOSEPH G HACIA
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依托单位:
COMPARATIVE GENOMICS OF PEROXISOMAL LIPID METABOLISM
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批准号:8171359
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项目类别:
-
资助金额:$0.24万
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财政年份:2010
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负责人:JOSEPH G HACIA
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依托单位:
COMPARATIVE GENOMICS OF PEROXISOMAL LIPID METABOLISM
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批准号:7723631
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项目类别:
-
资助金额:$0.08万
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财政年份:2008
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负责人:JOSEPH G HACIA
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依托单位:
Comparative Genomics of Peroxisomal Lipid Metabolism
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批准号:7392358
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项目类别:
-
资助金额:$30.63万
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财政年份:2005
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负责人:JOSEPH G HACIA
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依托单位:
Mutational Analysis of Peroxisome Biogenesis Disorders
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批准号:6953829
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项目类别:
-
资助金额:$22.01万
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财政年份:2005
-
负责人:JOSEPH G HACIA
-
依托单位:
Mutational Analysis of Peroxisome Biogenesis Disorders
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批准号:7140209
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项目类别:
-
资助金额:$17.96万
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财政年份:2005
-
负责人:JOSEPH G HACIA
-
依托单位:
Comparative Genomics of Peroxisomal Lipid Metabolism
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批准号:7217534
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项目类别:
-
资助金额:$28.59万
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财政年份:2005
-
负责人:JOSEPH G HACIA
-
依托单位:
Comparative Genomics of Peroxisomal Lipid Metabolism
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批准号:6920952
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项目类别:
-
资助金额:$34.37万
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财政年份:2005
-
负责人:JOSEPH G HACIA
-
依托单位:
Comparative Genomics of Peroxisomal Lipid Metabolism
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批准号:7046024
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项目类别:
-
资助金额:$30.76万
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财政年份:2005
-
负责人:JOSEPH G HACIA
-
依托单位:
Comparative Genomics of Peroxisomal Lipid Metabolism
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批准号:7589650
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项目类别:
-
资助金额:$31.55万
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财政年份:2005
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负责人:JOSEPH G HACIA
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依托单位:
GENE EXPRESSION PROFILING OF RHESUS STEM CELLS
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批准号:6940391
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项目类别:
-
资助金额:$1.42万
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财政年份:2003
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负责人:JOSEPH G HACIA
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依托单位:
海外基金