Characterization of Sleep Mutants of Drososphila
果蝇睡眠突变体的表征
基本信息
- 批准号:7264589
- 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 RhythmsCodeComplexDailyDataDevelopmentDrosophila genusDrosophila melanogasterExcisionFemaleGene ExpressionGene MutationGenesGeneticGenetic ScreeningGenomeGenomicsHeadHealthHourHumanIn Situ HybridizationLaboratoriesLightLinkLongevityMammalsMemoryMolecularMolecular GeneticsMolecular ProfilingMotor ActivityMusMutagenesisMutationNumbersPathway interactionsPatternPerformancePhenotypePhosphorusPhysiologicalPrincipal InvestigatorProtein OverexpressionProteinsQuantitative Trait LociRNA InterferenceRecoveryRegulationRelative (related person)ReportingResearchScreening procedureSequence HomologySleepSleep DeprivationStandards of Weights and MeasuresStressTestingTimeTransgenic OrganismsWakefulnessWestern Blottingbasebrain electrical activitycircadian pacemakerdayflygain of function mutationhypnoticinterestloss of function mutationmutantnovelprogramsresponsesleep 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。充足的睡眠是一种基本的生理需求。例如,减少正常睡眠者的睡眠时间会影响他们的表现、警觉性、记忆力和健康。像所有复杂的行为一样,睡眠是由环境调节和基因决定的。然而,负责的基因还没有被发现。为了确定它们,我们已经开始了一项基因筛查,在果蝇黑腹果蝇中寻找短睡眠者。果蝇中的突变筛选有助于揭示跨物种高度保守的细胞机制,例如控制发育,衰老,应激记忆和昼夜节律的细胞机制。在过去的几年里,我们的实验室和其他实验室已经证明,苍蝇的睡眠与哺乳动物的睡眠有许多关键特征。与哺乳动物一样,果蝇睡眠的特征是唤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,苍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。在过去的3年里,我们已经筛选了大约8000个突变株系,其中大部分携带单基因突变。我们发现,睡眠的数量和调节是高度保守的:几乎所有的果蝇睡眠时间在400到800分钟/24小时之间,并且在睡眠剥夺后睡眠时间和连续性增加。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),但这些线条显示出正常的白天表现和警惕性。当睡眠被剥夺时,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,这表明了单基因效应。我们建议从遗传、分子和行为三个方面来描述这三条线。我们将操纵负责短睡眠表型的基因的表达,研究由这些基因控制的分子通路,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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Chiara Cirelli其他文献
Chiara Cirelli的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Chiara Cirelli', 18)}}的其他基金
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:
8135372 - 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:
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:
7978917 - 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:
8472968 - 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:
相似国自然基金
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
- 批准号:JCZRQN202500010
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
- 批准号:2025JJ70209
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
- 批准号:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
- 批准号:2023JJ50274
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
- 批准号:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
- 批准号:
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
- 批准号:81973577
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
- 批准号:81602908
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
The Phenomenon of Stem Cell Aging according to Methylation Estimates of Age After Hematopoietic Stem Cell Transplantation
根据造血干细胞移植后甲基化年龄估算干细胞衰老现象
- 批准号:
23K07844 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Analysis of Age-dependent Functional Changes in Skeletal Muscle CB1 Receptors by an in Vitro Model of Aging-related Muscle Atrophy
通过衰老相关性肌肉萎缩的体外模型分析骨骼肌 CB1 受体的年龄依赖性功能变化
- 批准号:
22KJ2960 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Grant-in-Aid for JSPS Fellows
Joint U.S.-Japan Measures for Aging and Dementia Derived from the Prevention of Age-Related and Noise-induced Hearing Loss
美日针对预防与年龄相关和噪声引起的听力损失而导致的老龄化和痴呆症联合措施
- 批准号:
23KK0156 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Fund for the Promotion of Joint International Research (International Collaborative Research)
The Effects of Muscle Fatigability on Gait Instability in Aging and Age-Related Falls Risk
肌肉疲劳对衰老步态不稳定性和年龄相关跌倒风险的影响
- 批准号:
10677409 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Characterizing gut physiology by age, frailty, and sex: assessing the role of the aging gut in "inflamm-aging"
按年龄、虚弱和性别表征肠道生理学特征:评估衰老肠道在“炎症衰老”中的作用
- 批准号:
497927 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Role of AGE/RAGEsignaling as a driver of pathological aging in the brain
AGE/RAGE信号传导作为大脑病理性衰老驱动因素的作用
- 批准号:
10836835 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Elucidation of the protein kinase NLK-mediated aging mechanisms and treatment of age-related diseases
阐明蛋白激酶NLK介导的衰老机制及年龄相关疾病的治疗
- 批准号:
23K06378 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Underlying mechanisms of age-related changes in ingestive behaviors: From the perspective of the aging brain and deterioration of the gustatory system.
与年龄相关的摄入行为变化的潜在机制:从大脑老化和味觉系统退化的角度来看。
- 批准号:
23K10845 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Targeting Age-Activated Proinflammatory Chemokine Signaling by CCL2/11 to Enhance Skeletal Muscle Regeneration in Aging
通过 CCL2/11 靶向年龄激活的促炎趋化因子信号传导以增强衰老过程中的骨骼肌再生
- 批准号:
478877 - 财政年份:2023
- 资助金额:
$ 24.03万 - 项目类别:
Operating Grants














{{item.name}}会员




