The role of microRNAs in aging.
The role of microRNAs in aging.
批准号:
8140626
负责人:
Alexandre de Lencastre
金额:
$6.32万
依托单位:
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:
2009-08-01 至 2012-07-31
关键词:
AddressAdultAffectAgingAnimal GeneticsAnimal ModelAnimalsAreaBase PairingBioinformaticsBiologicalBiological AssayBiological MarkersBiological PhenomenaBiologyCaenorhabditis elegansCandidate Disease GeneCatalysisCloningDevelopmentDiseaseElementsEnvironmentEukaryotaExhibitsFamilyFunctional RNAGene ExpressionGene Expression RegulationGene SilencingGene TargetingGenesGeneticGenetic EpistasisGenetic SuppressionGenomeGoalsHumanImmunityLeadLengthLifeLongevityMalignant NeoplasmsMedical ResearchMicroRNAsMicroarray AnalysisMonitorMutateMutationNematodaNorthern BlottingOrganismPathway interactionsPatternPhenotypePhysiologicalPlantsPlayPopulationProteinsRNAReadingRegulationRegulatory ElementResearchReverse Transcriptase Polymerase Chain ReactionRoleSmall RNAStagingSurveysTechniquesTestingTimeTissuesUntranslated RegionsWorkagedbiological systemsinterestknockout genemembermutantneuron developmentnoveltransmission process
中文摘要
描述(由申请人提供):
英文摘要
DESCRIPTION (provided by applicant):
MicroRNAs (miRNAs) constitute a novel class of gene regulatory elements with important roles in the control of gene expression and development in plants and animals. miRNAs are endogenous, small non-coding RNAs which inhibit gene expression by base pairing with target genes and silencing their expression via mechanisms which are still being elucidated. Although highly abundant and predicted to target a wide proportion of genes in higher organisms, miRNAs have so far only been implicated in handful of biological roles. The function of the vast majority of miRNAs remains a mystery. Two founding members of the miRNA family, lin-4 and let-7, were first identified in the heterochronic pathway of C. elegans, which regulates the timing of larval development in the nematode. Both miRNAs have more recently been implicated in other biological areas, such as cancer and life span. Recent work has demonstrated that mutations to lin-4 and its target lin-14 significantly affect the lifespan of C. elegans. In addition, microarray analysis in C. elegans has revealed dynamic miRNA expression changes during aging. These observations suggest that miRNAs may function in pathways that impact life span. This proposal seeks to study the role of known miRNAs in aging, the identification of novel miRNAs in aged animals, and the genetic mechanisms underlying their function. In order to achieve these objectives, miRNAs will first be cloned from aged populations of C. elegans and from mutant worms that exhibit altered lifespan. The focus on enriched population of aged animals will allow the characterization of potential roles for new miRNAs in lifespan. Newly identified miRNAs as well as previously characterized heterochronic genes will then be mutated and assayed for lifespan effects in adult worms. We predict that yet unidentified miRNAs may modulate life span or serve as biomarkers of diseases of aging. Finally, in order to understand the genetic mechanisms underlying their role in aging, the downstream effects of mutations to these miRNAs will be studied by a variety of techniques including GFP:fusion expression analysis and epistastic relationship to genes in known life span pathways. Relevance: Understanding the biological mechanisms underlying aging is a key goal of current medical research. The short life span of the nematode C. elegans makes it the organism of choice in the study of aging. MicroRNAs, a novel class of regulatory elements first identified in C. elegans, have now been shown to modulate life span. We seek to identify new miRNAs with a role in aging and to study their function. Given the high conservation of microRNAs across species, findings from this research may lead to new biomarkers of diseases of aging and will inform on our understanding of aging in higher organisms and humans.
期刊论文(4)
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DOI:
10.1016/j.cub.2014.08.013
发表时间:
2014-10-06
期刊:
Current biology : CB
影响因子:
--
作者:
[Smith-Vikos T, de Lencastre A, Inukai S, Shlomchik M, Holtrup B, Slack FJ]
通讯作者:
Slack FJ
DOI:
10.1371/journal.pone.0040028
发表时间:
2012
期刊:
PloS one
影响因子:
3.7
作者:
[Inukai S, de Lencastre A, Turner M, Slack F]
通讯作者:
Slack F
DOI:
10.1016/j.cub.2010.11.015
发表时间:
2010-12-21
期刊:
CURRENT BIOLOGY
影响因子:
9.2
作者:
[de Lencastre, Alexandre, Pincus, Zachary, Zhou, Katherine, Kato, Masaomi, Lee, Siu Sylvia, Slack, Frank J.]
通讯作者:
Slack, Frank J.
DOI:
10.1007/978-1-4939-2963-4_18
发表时间:
2015
期刊:
Methods in molecular biology
影响因子:
--
作者:
[A. de Lencastre;F. Slack]
通讯作者:
A. de Lencastre;F. Slack
Molecular Mechanisms of miRNA Function in Stress Response and in Models of Diseases of Aging in C. elegans
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批准号:8958261
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项目类别:
-
资助金额:$27.84万
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财政年份:2015
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负责人:Alexandre de Lencastre
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依托单位:
The role of microRNAs in aging.
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批准号:7991789
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项目类别:
-
资助金额:$6.03万
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财政年份:2009
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负责人:Alexandre de Lencastre
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依托单位:
海外基金