The regulation of gut-brain communication during Caenorhabditis elegans dauer development
The regulation of gut-brain communication during Caenorhabditis elegans dauer development
批准号:
10152625
负责人:
Mengyi Cao
金额:
$6.86万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-05-01 至 2022-04-30
关键词:
AcidsAnabolismAnimal BehaviorAnimal ModelAnimalsBrainCaenorhabditis elegansCommunicationDataDecision MakingDevelopmentDiapauseDiseaseEnvironmentFluorescenceGastrointestinal tract structureGene Expression ProfileGenesGenetic RecombinationGenetic TranscriptionGoalsGrowth FactorHormonesImmunityIndividualInsulinIntestinesIrritable Bowel SyndromeKnowledgeLifeLigandsLiteratureMental HealthMetabolismModelingMolecularMolecular GeneticsNematodaNervous system structureNeuroendocrine CellOrganParkinson DiseasePathway interactionsPhysiologyProcessPublishingRegulationRegulator GenesRegulatory PathwayReporterReportingResearchRoleSignal PathwaySignal TransductionSiteStressSystemTestingTissuesTransforming Growth Factor betaTranslationsWhole Organismassay developmentbasefood shortagegut-brain axisimprovedoverpopulationphysical conditioningpromoterreceptorresponsespatiotemporaltooltranscription factor S-II
中文摘要
项目摘要
不同组织(或器官)之间的通讯,如肠-脑轴,在调节
动物生理学和发育决策。线虫秀丽隐杆线虫进入一个非进食,
发育停滞的dauer阶段,以科普恶劣的环境,如食物短缺和过度-
人口Dauer决策受多种途径(胰岛素、生长因子和激素)调节,
涉及神经系统、XXX神经内分泌细胞和肠。先前的研究已经建立了
C.线虫作为模式生物研究应激反应的发展,但组织特异性调节
Dauer的发展仍不清楚。特别是,很少有人知道神经系统如何协调,
肠道整合信号通路,并作出整个有机体的dauer决定。拟议
目的是提供一个系统的研究,不同的组织如何通过多个
信号通路,并利用分子遗传学工具协调调节dauer决策
最近在赞助商实验室研发的为了实现这一目标,Aim 1将重点调查
每个组织在dauer发展过程中的作用,并建立调控网络的模型;目标2将侧重于
每个组织和每个通路在Dauer决策启动和执行中的时间参与,还
开发出精确的道尔调节电路。总之,拟议的目标将扩大目前的
了解滞育发生时间的分子机制
to environmental环境stress应力.利用C. elegans dauer决定作为一个模型,建议的项目将有助于
更好地了解组织间的协调,特别是在脑肠道通信,在
发展决策过程。
英文摘要
Project Summary
The communication among different tissues (or organs), such as the gut-brain axis, is crucial in regulating
animal physiology and developmental decisions. The nematode Caenorhabditis elegans enters a non-feeding,
developmentally arrested dauer stage to cope with the harsh environments, such as food shortage and over-
population. The dauer decision is regulated by the multiple pathways (insulin, growth factor, and hormone),
involving the nervous system, XXX neuroendocrine cells, and intestine. Previous research has established
C. elegans as a model organism to study stress-responsive development, but tissue-specific regulation of
dauer development remains unclear. In particular, little is known about how nervous system coordinates with
the intestine to integrate the signaling pathways and make a whole-organism dauer decision. The proposed
aims focus on providing a systematic study of how different tissues communicate through multiple
signaling pathways and coordinately regulate the dauer decision using molecular genetics tools
recently developed in the sponsor lab. To achieve this goal, Aim 1 will focus on investigating the general
roles of each tissue during dauer development and build models for the regulatory network; Aim 2 will focus on
temporal participation of each tissue and each pathway in dauer decision initiation and execution, further
developing precise circuits of dauer regulation. Altogether, the proposed aims will expand the current
knowledge of molecular mechanisms underlying developmental timing of commitment to diapause in response
to environmental stress. Using C. elegans dauer decision as a model, the proposed project will contribute to
better understanding of the inter-tissue coordination, particularly in brain-gut communication, during the
developmental decision making process.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Effects of ASD-associated daf-18/PTEN missense variants on C. elegans dauer development.
ASD 相关的 daf-18/PTEN 错义变异对秀丽隐杆线虫 dauer 发育的影响。
DOI:
10.17912/micropub.biology.000177
发表时间:
2019
期刊:
microPublication biology
影响因子:
--
作者:
[González-Cavazos,Carolina, Cao,Mengyi, Wong,Wan-Rong, Chai,Cynthia, Sternberg,Paul]
通讯作者:
Sternberg,Paul
海外基金