Roles of small RNAs in guarding germ cell genomes
Roles of small RNAs in guarding germ cell genomes
批准号:
8915706
负责人:
Gregory J Hannon
金额:
$39.56万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-15 至 2018-08-31
关键词:
AddressAffectAnimalsAreaBerylliumBindingBiochemicalBiochemistryBiogenesisBiologicalBiological ProcessCell NucleusCell physiologyCellsChromatinChromosome SegregationCleaved cellCodeComplexConsensusCytoplasmDNA Insertion ElementsDefense MechanismsDepositionDrosophila genusElementsEpigenetic ProcessEventFailureFamilyFundingGene ExpressionGenesGenetic TranscriptionGenomeGenomicsGerm CellsGerm LinesGoalsHealthHost-Parasite RelationsImmune systemInheritedLeadMechanicsMessenger RNAMobile Genetic ElementsModelingMolecularMusNuclearOrganismParasitesParentsPathway interactionsPlant RootsPlayPopulationProcessProductionProgress ReportsProtein FamilyProteinsRegulationReplication ErrorRepressionRoleSignal TransductionSiteSmall RNAStagingSterilityTissuesTranscriptWorkbasecofactorflygenetic elementinsightneuronal cell bodynoveloffspringpiRNAreproductiveresponsetransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
It is essential that the genome be passed faithfully from parents to their offspring. Threats to faithful genome transmission come from limitations on the fidelity of replication, errors in chromosome segregation, and from the deleterious activity of parasitic genetic elements, transposons, which propagate by increasing their copy numbers in germ cell genomes. The challenge of transposon control is formidable. In Drosophila, more than 200 different elements are distributed among highly divergent families. These elements use different mobilization strategies and share no universal proteins or cofactors. Thus, the host must somehow discriminate this diversity of elements from protein coding genes and selectively silence the former. Over the past 6 years, we have come to understand that the piRNA pathway plays a critical role in reproductive tissues, embodying an essential defense mechanism against mobile genetic elements. Studies, mainly in Drosophila and mice, have established a molecular framework for how the piRNA pathway operates and have implicated a growing list of protein cofactors in its various stages. While we have produced a coarse model for piRNA production and for the mechanisms by which the pathway silences transposons, we are only just beginning to understand many of the molecular events that form the mechanistic basis of this innate immune system Our goal in this proposal is to address three key, outstanding issues. First, we wish to understand how the definition of a transposon is established in the form of a piRNA repertoire. This entails deciphering the regulation of piRNA generative loci, the mechanisms which mark RNAs to be processed into piRNAs, and the mechanics of piRNA biogenesis. Second, we will uncover the biochemistry of target repression by Piwi protein/piRNA complexes at both the transcriptional and post-transcriptional levels. Third, will probe the functions of maternally inherited piRNAs and their roles in germ cells and in the soma. By accomplishing these aims, we will contribute to the understanding of one of the most deeply rooted biological imperatives, the need to conserve the integrity of the germ line
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会议论文
An optogenetic toolkit for the interrogation and control of single cells.
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批准号:8822629
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项目类别:
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资助金额:$45.24万
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财政年份:2014
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负责人:Gregory J Hannon
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依托单位:
Project 4
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批准号:8744320
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项目类别:
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资助金额:$64.73万
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财政年份:2013
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负责人:Gregory J Hannon
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依托单位:
Core B
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批准号:8744323
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项目类别:
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资助金额:$34.98万
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财政年份:2013
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负责人:Gregory J Hannon
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依托单位:
Core A
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批准号:8744322
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项目类别:
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资助金额:$21.43万
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财政年份:2013
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负责人:Gregory J Hannon
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依托单位:
Modulation of Gene Expression Through RNAi
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批准号:8234421
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项目类别:
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资助金额:$36.49万
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财政年份:2012
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负责人:Gregory J Hannon
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依托单位:
Administration
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批准号:8234420
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项目类别:
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资助金额:$23.4万
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财政年份:2012
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负责人:Gregory J Hannon
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依托单位:
Acquisition of a high-throughput compute cluster for biological data analysis
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批准号:8247532
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项目类别:
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资助金额:$51.98万
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财政年份:2012
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负责人:Gregory J Hannon
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依托单位:
microRNAs in Human Cancer
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批准号:8234414
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项目类别:
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资助金额:$66.63万
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财政年份:2012
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负责人:Gregory J Hannon
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依托单位:
A ROLE FOR THE P-BODY COMPONENT GW182 IN MICRORNA FUNCTION
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批准号:8171361
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项目类别:
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资助金额:$0.08万
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财政年份:2010
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负责人:Gregory J Hannon
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依托单位:
Cold Spring Harbor Laboratory Cancer Research Center
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批准号:7910927
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项目类别:
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资助金额:$9.93万
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财政年份:2009
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负责人:Gregory J Hannon
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依托单位:
Administration
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批准号:7225422
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项目类别:
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资助金额:$24.98万
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财政年份:2007
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负责人:Gregory J Hannon
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依托单位:
microRNAs in Human Cancer
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批准号:7225420
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项目类别:
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资助金额:$58.73万
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财政年份:2007
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负责人:Gregory J Hannon
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依托单位:
Modulation of Gene Expression Through RNAi
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批准号:7225423
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项目类别:
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资助金额:$42.6万
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财政年份:2007
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负责人:Gregory J Hannon
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依托单位:
A ROLE FOR THE P-BODY COMPONENT GW182 IN MICRORNA FUNCTION
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批准号:7420742
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项目类别:
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资助金额:$0.29万
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财政年份:2006
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负责人:Gregory J Hannon
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依托单位:
Conference on Roles of RNA in Gene Regulation
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批准号:6884302
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项目类别:
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资助金额:$1.0万
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财政年份:2005
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负责人:Gregory J Hannon
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依托单位:
Phenotype Arrays--An approach to Novel Anticancer Target
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批准号:6515040
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项目类别:
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资助金额:$16.6万
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财政年份:2001
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负责人:Gregory J Hannon
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依托单位:
Phenotype Arrays--An approach to Novel Anticancer Target
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批准号:6331975
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项目类别:
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资助金额:$16.64万
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财政年份:2001
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负责人:Gregory J Hannon
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依托单位:
MECHANISMS OF DSRNA-INDUCED GENE SILENCING
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批准号:6254783
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项目类别:
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资助金额:$28.33万
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财政年份:2000
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负责人:Gregory J Hannon
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依托单位:
Mechanisms of dsRNA-induced gene silencing
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批准号:6986416
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项目类别:
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资助金额:$36.44万
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财政年份:2000
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负责人:Gregory J Hannon
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依托单位:
MECHANISMS OF DSRNA-INDUCED GENE SILENCING
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批准号:6798062
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项目类别:
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资助金额:$2.54万
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财政年份:2000
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负责人:Gregory J Hannon
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依托单位:
海外基金