Characterization of Sleep Mutants of Drososphila
果蝇睡眠突变体的表征
基本信息
- 批准号:7666907
- 负责人:
- 金额:$ 24.03万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-08-01 至 2010-07-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAgeAgingArousalBehaviorBiologicalBiological ModelsBrainChromosomes, Human, Pair 1Circadian RhythmsCodeComplexDataDevelopmentDrosophila genusDrosophila melanogasterExcisionFemaleGene ExpressionGene MutationGenesGeneticGenetic ScreeningGenomeGenomicsHeadHealthHourHumanIn Situ HybridizationLaboratoriesLightLinkLongevityMammalsMemoryMolecularMolecular GeneticsMolecular ProfilingMotor ActivityMusMutagenesisMutationPathway interactionsPatternPerformancePhenotypePhosphorusPhysiologicalPrincipal InvestigatorProteinsQuantitative Trait LociRNA InterferenceRecoveryRegulationRelative (related person)ReportingResearchScreening procedureSequence HomologySleepSleep DeprivationStressTestingTimeTransgenic OrganismsWakefulnessWestern Blottingbasebrain electrical activitycircadian pacemakerflygain of function mutationhypnoticinterestloss of function mutationmutantnoveloverexpressionprogramsresponsesleep regulationvigilance
项目摘要
DESCRIPTION (provided by applicant): Sleep is present in all species where it has been studied, but its functions remain unknown. A sufficient amount of sleep constitutes a fundamental biological need. For example, curtailing the amount of sleep in normal sleepers affects performance, vigilance, memory and health. Like all complex behaviors, sleep is both environmentally modulated and genetically determined. However, the responsible genes have not been discovered. To identify them, we have initiated a genetic screening for short sleepers in the fruit fly Drosophila melanogaster. Mutagenesis screening in Drosophila has helped unraveling cellular mechanisms that are highly conserved across species, e.g. those controlling development, aging, stress memory, and circadian rhythms. Over the past few years, our laboratory and others have shown that fly sleep shares many key features with mammalian sleep. As in mammals, sleep in Drosophila is characterized by increased arousal thresholds and by changes in brain electrical activity. Fly sleep is regulated independent of the circadian clock, is modulated by stimulants and hypnotics, and is affected by age. Also, fly sleep is associated with changes in brain gene expression similar to those observed in mammals. Over the past 3 years, we have screened approximately 8000 mutant lines, most of which carry single-gene mutations. We found that the amount and regulation of sleep are highly conserved: almost all flies sleep between 400 and 800 min/24 hours and show increased sleep duration and continuity after sleep deprivation. We have also identified several short sleeper lines, three of which are particularly interesting. Despite the reduced amount of sleep (<230 min/day), these lines show normal day-time performance and vigilance. When sleep deprived, they recover most of the sleep lost, suggesting that it is biologically important. The short sleep mutation is due to the genomic insertion of a P element whose mobilization reverts them to normal sleep, suggesting a single gene effect. We propose to characterize these three lines genetically, molecularly, and behaviorally. We will manipulate the expression of the genes responsible for the short sleep phenotype, investigate the molecular pathways controlled by these genes, and characterize their impact on performance, memory, circadian rhythms and life span. This research will help to identify the molecular mechanisms regulating the need for sleep and provide novel clues to its functions.
描述(由申请人提供):睡眠存在于所有研究过的物种中,但其功能仍然未知。充足的睡眠是基本的生物需求。例如,减少正常睡眠者的睡眠时间会影响表现、警觉性、记忆力和健康。与所有复杂的行为一样,睡眠既受环境调节,又受基因决定。然而,尚未发现相关基因。为了识别它们,我们启动了对果蝇中短睡眠者的基因筛查。果蝇的诱变筛选有助于揭示跨物种高度保守的细胞机制,例如。那些控制发育、衰老、压力记忆和昼夜节律的细胞。在过去的几年里,我们的实验室和其他实验室已经证明,果蝇的睡眠与哺乳动物的睡眠有许多共同的关键特征。与哺乳动物一样,果蝇的睡眠特点是觉醒阈值增加和脑电活动变化。果蝇睡眠的调节独立于生物钟,受兴奋剂和催眠药的调节,并受年龄的影响。此外,果蝇睡眠与大脑基因表达的变化有关,类似于在哺乳动物中观察到的变化。过去3年,我们筛选了大约8000个突变株系,其中大部分携带单基因突变。我们发现睡眠的量和调节是高度保守的:几乎所有果蝇的睡眠时间在 400 至 800 分钟/24 小时之间,并且在睡眠剥夺后表现出睡眠持续时间和连续性的增加。我们还确定了几条短卧铺线路,其中三条特别有趣。尽管睡眠量减少(<230 分钟/天),这些线仍显示出正常的白天表现和警惕性。当睡眠不足时,他们会恢复大部分失去的睡眠,这表明睡眠在生物学上很重要。短睡眠突变是由于基因组中插入了一个 P 元件,该元件的动员使它们恢复正常睡眠,这表明单基因效应。我们建议从遗传、分子和行为上表征这三个系。我们将操纵导致短睡眠表型的基因的表达,研究这些基因控制的分子途径,并表征它们对表现、记忆、昼夜节律和寿命的影响。这项研究将有助于确定调节睡眠需求的分子机制,并为其功能提供新的线索。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Chiara Cirelli其他文献
Chiara Cirelli的其他文献
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{{ truncateString('Chiara Cirelli', 18)}}的其他基金
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical Time
神经发育中的突触和睡眠:关键时刻的关键相互作用
- 批准号:
8288301 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical Time
神经发育中的突触和睡眠:关键时刻的关键相互作用
- 批准号:
8471198 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical Time
神经发育中的突触和睡眠:关键时刻的关键相互作用
- 批准号:
8135372 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Brain Plasticity and Local Sleep Homeostasis: A Molecular Perspective
大脑可塑性和局部睡眠稳态:分子视角
- 批准号:
8118162 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical Time
神经发育中的突触和睡眠:关键时刻的关键相互作用
- 批准号:
8472968 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical Time
神经发育中的突触和睡眠:关键时刻的关键相互作用
- 批准号:
7978917 - 财政年份:2010
- 资助金额:
$ 24.03万 - 项目类别:
Brain Plasticity and Local Sleep Homeostasis: A Molecular Perspective
大脑可塑性和局部睡眠稳态:分子视角
- 批准号:
7346830 - 财政年份:2007
- 资助金额:
$ 24.03万 - 项目类别:
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