Engrailed and the control of synaptic circuits in adult Drosophila
Engrailed and the control of synaptic circuits in adult Drosophila
批准号:
9922928
负责人:
JONATHAN M BLAGBURN
金额:
$11.25万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-05-01 至 2022-04-30
关键词:
Action PotentialsAdultAfferent NeuronsAgeAnatomyAnimalsArthropodsAuditoryAuditory systemBehaviorBinding ProteinsBiological AssayBiological ModelsBrainBrain DiseasesBranchiostoma floridae AmphiEn proteinCell surfaceCharacteristicsChemicalsChestCoupledDNADetectionDevelopmentDiseaseDrosophila genusDrosophila melanogasterDyesEarElectrophysiology (science)EvolutionFemaleFiberGap JunctionsGene ExpressionGenesGeneticGenetic MarkersGoalsHeadHealthHomeodomain ProteinsHumanImage AnalysisInterneuronsLabelLifeLinkLongevityLoveMaintenanceMeasuresMediatingMethodsModelingMolecularNeuraxisNeuronsOrganOutputParkinson DiseasePartner in relationshipPathway interactionsPatternPhenotypePlayProcessProteinsPublic HealthPupaRecoveryResearchRoleSex DifferencesSpecificityStainsSynapsesTechniquesTemperatureTestingTimeWorkage relatedautism spectrum disorderelectrical propertyexperimental studyflyhuman diseaseknock-downmalemature animalnerve injuryneural circuitneuron developmentneuronal circuitryneuronal excitabilitypresynapticquantitative imagingsexsynaptic functionsynaptogenesistranscription factor
中文摘要
摘要
Engrailed(En)是一种转录因子;一种与DNA结合并打开或关闭其他基因的蛋白质。它
最初在果蝇中发现,但后来发现存在于所有动物中,在其中起着重要作用
控制神经元或神经细胞的发育。这项研究的长期目标是找出如何
En控制着大脑中神经细胞相互连接(形成突触)的方式,
专注于识别和表征它所调控的基因和分子网络。这项建议
使用果蝇听觉神经元-巨纤维(GF)突触作为模型系统,
研究En在控制突触连接中的作用。第一个具体目标将是使用
电生理学和解剖染色技术来测量听觉神经元动作电位和
随着动物年龄的增长,GF的输出突触发生变化,并确定是否存在性别特异性
差异第二个具体目标将是研究改变存在于纳米颗粒中的En的量的影响。
成年动物的神经元。与哺乳动物神经元一样,果蝇听觉神经元中En的表达持续存在
它在成年后的生活中,但它在这一时期的功能还不清楚。它也许可以维持他们的
电特性或它们突触连接的模式。为了验证这一点,遗传学方法将被用来
在不同的时间从感觉神经元增加或减少En。
这项工作与公共卫生有关,因为人类En与几种大脑疾病有关,例如
帕金森氏症和自闭症。果蝇模型对于发现分子生物学中的
与人类直接相关的途径,因为这些途径中的大多数在
进化所有的动物都有En蛋白,所以很有可能在哺乳动物的发育过程中,
果蝇的突触形成过程在人类中也有类似的过程,在大脑中扮演着类似的角色
发展
英文摘要
Abstract
Engrailed (En) is a transcription factor; a protein that binds to DNA and that switches on or off other genes. It
was first discovered in Drosophila but later found to be present in all animals, where it plays an important role
in controlling the development of neurons, or nerve cells. The long-term goal of this research is to find out how
En controls the way that nerve cells connect to each other (form synapses) within the brain, with a particular
focus on identifying and characterizing the network of genes and molecules that it regulates. This proposal
uses the Drosophila auditory neuron – to – giant fiber (GF) synapse as a model system with which to
investigate the role of En in the control of synaptic connections. The first specific aim will be to use
electrophysiology and anatomical staining techniques to measure how auditory neuron action potentials and
output synapses to the GF change as the animal ages, and to determine whether there are sex-specific
differences. The second specific aim will be to study the effects of changing the amounts of En present in the
neurons in the adult animal. As in mammalian neurons, En expression in Drosophila auditory neurons persists
through adult life, but its functions during this period are not understood. It could perhaps maintain their
electrical properties or the patterns of their synaptic connections. To test this, genetic methods will be used to
add or take away En from the sensory neurons at different times.
This work is relevant to public health because human En has been linked to several brain disorders, such as
Parkinson’s disease and autism. Drosophila models are particularly useful for the discovery of molecular
pathways that are directly relevant to humans, because most of these pathways have been conserved during
evolution. All animals have En protein, so it is very likely that any molecules that are regulated by it during the
process of synapse formation in Drosophila have their counterparts in humans, playing similar roles in brain
development.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Engrailed targets and the control of synaptic circuits in Drosophila
-
批准号:8468764
-
项目类别:
-
资助金额:$36.19万
-
财政年份:2012
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed targets and the control of synaptic circuits in Drosophila
-
批准号:8657495
-
项目类别:
-
资助金额:$37.13万
-
财政年份:2012
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed targets and the control of synaptic circuits in Drosophila
-
批准号:8843056
-
项目类别:
-
资助金额:$37.5万
-
财政年份:2012
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed targets and the control of synaptic circuits in Drosophila
-
批准号:8257801
-
项目类别:
-
资助金额:$35.21万
-
财政年份:2012
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed and the Control of Synaptic Circuitry in Drosophila
-
批准号:7497678
-
项目类别:
-
资助金额:$11.25万
-
财政年份:2008
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed and the Control of Synaptic Circuitry in Drosophila
-
批准号:7683182
-
项目类别:
-
资助金额:$11.25万
-
财政年份:2008
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
Engrailed and the Control of Synaptic Circuitry in Drosophila
-
批准号:7896492
-
项目类别:
-
资助金额:$11.25万
-
财政年份:2008
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
-
批准号:6496791
-
项目类别:
-
资助金额:$24.35万
-
财政年份:2001
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
-
批准号:6338922
-
项目类别:
-
资助金额:$18.58万
-
财政年份:2000
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
-
批准号:6273599
-
项目类别:
-
资助金额:$1.03万
-
财政年份:1998
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
SPECIFICITY AND PLASTICITY OF DEVELOPING SYNAPSES
-
批准号:6112004
-
项目类别:
-
资助金额:$2.33万
-
财政年份:1997
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
-
批准号:6243384
-
项目类别:
-
资助金额:$9.31万
-
财政年份:1997
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
SPECIFICITY AND PLASTICITY OF DEVELOPING SYNAPSES
-
批准号:6593349
-
项目类别:
-
资助金额:$25.66万
-
财政年份:1976
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
SPECIFICITY AND PLASTICITY OF DEVELOPING SYNAPSES
-
批准号:6651612
-
项目类别:
-
资助金额:$26.39万
-
财政年份:1976
-
负责人:JONATHAN M BLAGBURN
-
依托单位:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
-
批准号:5215000
-
项目类别:
-
资助金额:$0.0万
-
财政年份:--
-
负责人:JONATHAN M BLAGBURN
-
依托单位:--
海外基金