Molecular mechanisms governing maintenance of neural identity
控制神经同一性维持的分子机制
基本信息
- 批准号:7679726
- 负责人:
- 金额:$ 4.62万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-07-22 至 2012-07-21
- 项目状态:已结题
- 来源:
- 关键词:AdolescenceAdultAffectAttentionBindingBiological AssayBiological Neural NetworksBiological ProcessBrainButanonesCaenorhabditis elegansCell CommunicationCell NucleusCell membraneCellsCharacteristicsChemicalsChildhoodCloningCognitionCommunitiesComplexContralateralCuesCyclic GMPCytoplasmDataDetectionDevelopmentDiseaseEnsureEnvironmentEsthesiaFailureGenesGeneticGenetic ScreeningGenetic TranscriptionGerm CellsGoalsHomeodomain ProteinsHourHumanIn VitroIndividualLeftLocationMaintenanceMental disordersModificationMolecularMutationNematodaNervous System PhysiologyNervous system structureNeuronsNuclear ProteinNuclear ProteinsOdorsPathway interactionsPatternPhenotypePlayPreventionProcessPropertyProteinsPsychological reinforcementPublic HealthRegulationRepressionRoleSchizophreniaSensorySignal TransductionSignal Transduction PathwaySiteSpecific qualifier valueStagingStimulusSystemTimeTranscriptional Regulationbasecell typeextracellularhatchingin vivomature animalmolecular markermutantolfactory stimulusprogramspromoterrelating to nervous systemtime interval
项目摘要
DESCRIPTION (provided by applicant): Precise cellular identities are necessary to maintain a coherent network of communicating neurons. In the human brain, neural networks are constructed in a well-controlled manner and then subjected to multiple iterations of reinforcement and modulation, resulting in a system capable of adult cognition. Much of this refinement takes place during childhood and adolescence, in the context of interactions with the environment. Throughout this process, specific cells establish unique identities within the network; their roles are dependent both on the initial cell type, defined by an early developmental program, and on the modifications that occur as they become integrated into the nervous system as a whole. If a neuron cannot retain its initial, fundamental characteristics as it adapts itself to the network developing around it, its role in the system may be corrupted. This study aims to examine the molecular means by which a neuron maintains crucial aspects of its identity in a changing environment. Because multiple undefined inputs to a cell may be difficult to control and their effects may be difficult to track, this study makes use of a system in which stimuli are well defined, and markers of cell identity are easy to follow. The AWC olfactory neurons in the nematode C. elegans detect a defined set of volatile chemicals and can be identified by a specific set of molecular markers. The goal of this study is to identify and characterize molecules responsible for maintaining neural identity in the AWCs after differentiation, when the neurons are first exposed to external olfactory stimuli. Specifically, this study aims to: (1) determine the mechanism of action of the nuclear protein, NSY-7, which is required for one of the AWC neurons to retain aspects of its identity after differentiation; (2) characterize the expression and regulation of the nsy-7 gene in order to better understand its function, and (3) define interactions between nsy-7 and the molecular pathway responsible for sensory signal transduction in the AWCs. Examination of the mechanisms controlling maintenance of neural identity may serve to illuminate the factors involved in certain psychiatric disorders, such as schizophrenia, that appear to be partially under genetic control but that first manifest themselves at or after adolescence. The factors responsible for the failure of an apparently normal brain to attain stability late in development remain largely unidentified, but disorders in which an seemingly stable brain departs from its normal state are widespread. Elucidation of the genes that normally control this phenomenon, and their application in the treatment and prevention of psychiatric disease, would therefore be broadly beneficial to public health and to the community.
描述(由申请人提供):准确的细胞身份是维持一个连贯的通信神经元网络所必需的。在人脑中,神经网络是以一种受控良好的方式构建的,然后经历多次强化和调制的迭代,从而形成一个能够进行成人认知的系统。这种改进在很大程度上发生在儿童和青春期,在与环境互动的背景下。在整个过程中,特定的细胞在网络中建立独特的身份;它们的角色取决于由早期发育程序定义的初始细胞类型,以及当它们作为一个整体整合到神经系统时发生的修改。如果神经元在适应周围发展的网络时不能保持其初始的、基本的特征,那么它在系统中的作用可能会被破坏。这项研究旨在研究神经元在不断变化的环境中保持其身份的关键方面的分子手段。由于对一个细胞的多个不确定的输入可能很难控制,它们的影响也可能很难跟踪,因此本研究利用了一个系统,其中刺激定义得很好,细胞身份的标记很容易跟踪。线虫体内的AWC嗅觉神经元检测到一组定义的挥发性化学物质,并可以通过一组特定的分子标记进行识别。本研究的目的是确定和表征在AWCs分化后,当神经元首次暴露于外部嗅觉刺激时,负责维持神经同一性的分子。具体地说,本研究旨在:(1)确定核蛋白NSY-7的作用机制,NSY-7是AWC神经元在分化后保持其某些特性所必需的;(2)表征NSY-7基因的表达和调控,以便更好地了解其功能;以及(3)确定NSY-7与AWC中负责感觉信号转导的分子通路之间的相互作用。对控制神经同一性维持的机制的研究可能有助于阐明某些精神障碍所涉及的因素,例如精神分裂症,这些疾病似乎部分受基因控制,但在青春期或青春期后首次显现。看似正常的大脑在发育后期未能获得稳定的原因在很大程度上仍未确定,但看似稳定的大脑偏离正常状态的疾病普遍存在。因此,阐明通常控制这一现象的基因及其在治疗和预防精神疾病方面的应用,将广泛有益于公众健康和社区。
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 }}
Bluma J Lesch其他文献
Bluma J Lesch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('Bluma J Lesch', 18)}}的其他基金
Defining the role of DOT1L in chromocenter stabilization pre- and post-fertilization
定义 DOT1L 在受精前后染色中心稳定中的作用
- 批准号:
10739438 - 财政年份:2023
- 资助金额:
$ 4.62万 - 项目类别:
Germline Utx mutation as a model for transgenerational epigenetic inheritance
种系 Utx 突变作为跨代表观遗传的模型
- 批准号:
9885389 - 财政年份:2020
- 资助金额:
$ 4.62万 - 项目类别:
Germline Utx mutation as a model for transgenerational epigenetic inheritance
种系 Utx 突变作为跨代表观遗传的模型
- 批准号:
10558630 - 财政年份:2020
- 资助金额:
$ 4.62万 - 项目类别:
Sex chromosome control of chromatin in the gametes
配子中染色质的性染色体控制
- 批准号:
8655456 - 财政年份:2013
- 资助金额:
$ 4.62万 - 项目类别:
Sex chromosome control of chromatin in the gametes
配子中染色质的性染色体控制
- 批准号:
8525607 - 财政年份:2013
- 资助金额:
$ 4.62万 - 项目类别:
Molecular mechanisms governing maintenance of neural identity
控制神经同一性维持的分子机制
- 批准号:
7536310 - 财政年份:2008
- 资助金额:
$ 4.62万 - 项目类别:
相似海外基金
Co-designing a lifestyle, stop-vaping intervention for ex-smoking, adult vapers (CLOVER study)
为戒烟的成年电子烟使用者共同设计生活方式、戒烟干预措施(CLOVER 研究)
- 批准号:
MR/Z503605/1 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Research Grant
Early Life Antecedents Predicting Adult Daily Affective Reactivity to Stress
早期生活经历预测成人对压力的日常情感反应
- 批准号:
2336167 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Standard Grant
RAPID: Affective Mechanisms of Adjustment in Diverse Emerging Adult Student Communities Before, During, and Beyond the COVID-19 Pandemic
RAPID:COVID-19 大流行之前、期间和之后不同新兴成人学生社区的情感调整机制
- 批准号:
2402691 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Standard Grant
Elucidation of Adult Newt Cells Regulating the ZRS enhancer during Limb Regeneration
阐明成体蝾螈细胞在肢体再生过程中调节 ZRS 增强子
- 批准号:
24K12150 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Migrant Youth and the Sociolegal Construction of Child and Adult Categories
流动青年与儿童和成人类别的社会法律建构
- 批准号:
2341428 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Standard Grant
Understanding how platelets mediate new neuron formation in the adult brain
了解血小板如何介导成人大脑中新神经元的形成
- 批准号:
DE240100561 - 财政年份:2024
- 资助金额:
$ 4.62万 - 项目类别:
Discovery Early Career Researcher Award
RUI: Evaluation of Neurotrophic-Like properties of Spaetzle-Toll Signaling in the Developing and Adult Cricket CNS
RUI:评估发育中和成年蟋蟀中枢神经系统中 Spaetzle-Toll 信号传导的神经营养样特性
- 批准号:
2230829 - 财政年份:2023
- 资助金额:
$ 4.62万 - 项目类别:
Standard Grant
Usefulness of a question prompt sheet for onco-fertility in adolescent and young adult patients under 25 years old.
问题提示表对于 25 岁以下青少年和年轻成年患者的肿瘤生育力的有用性。
- 批准号:
23K09542 - 财政年份:2023
- 资助金额:
$ 4.62万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Identification of new specific molecules associated with right ventricular dysfunction in adult patients with congenital heart disease
鉴定与成年先天性心脏病患者右心室功能障碍相关的新特异性分子
- 批准号:
23K07552 - 财政年份:2023
- 资助金额:
$ 4.62万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Issue identifications and model developments in transitional care for patients with adult congenital heart disease.
成人先天性心脏病患者过渡护理的问题识别和模型开发。
- 批准号:
23K07559 - 财政年份:2023
- 资助金额:
$ 4.62万 - 项目类别:
Grant-in-Aid for Scientific Research (C)