Genetic Mechanisms of Hindbrain Segmentation
Genetic Mechanisms of Hindbrain Segmentation
批准号:
7638474
负责人:
Cecilia B Moens
金额:
$29.2万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-06-01 至 2012-05-31
关键词:
AddressAdhesionsAffectAnimalsAppearanceBehaviorBrain regionCell SeparationCell-Cell AdhesionCellsDevelopmentDiffuseDrosophila genusEmbryoEnvironmentGenesGeneticGoalsMaintenanceMediatingMethodsMolecularNervous system structureNeuraxisPatternPopulationPositioning AttributePropertyResearchResearch PersonnelSeriesSideSignal PathwaySignal TransductionSorting - Cell MovementSystemTestingTissuesTo specifyTretinoinTweensZebrafishbasegene functionhindbrainmutantneuroepitheliumparallel processingprogramsresponse
中文摘要
描述(由申请人提供):组织之间或组织内边界的形成是动物发育的一个基本方面。边界的功能是将具有不同身份的细胞群体分开,使它们能够遵循独立的发育程序,尽管它们非常接近。此外,边界可以形成重要的组织中心,使相邻细胞形成图案。在发育中的脊椎动物中枢神经系统中,边界形成于明显同质的神经上皮中,将随后获得不同组织学和功能特性的脑区域分开。特别是在后脑中,菱形之间形成边界,沿着主体轴产生一系列沿着7节。尽管边界在动物发育中至关重要,但令人惊讶的是,人们对控制边界形成的分子和机制知之甚少。即使在果蝇中,隔室边界已经引起了研究人员几十年的兴趣,但介导边界形成的实际分子最近才开始被阐明。这项研究的长期目标是了解脊椎动物后脑发育过程中菱形节边界形成和维持的细胞和分子基础。我们知道,一个尖锐的发展边界的出现涉及两个步骤:第一,长距离信号建立广泛的域与不同的区域身份,但扩散的边界,其次,在这些域的边缘细胞之间的精细尺度的相互作用,导致边界的锐化。在本提案的目标1和2中,我们通过研究两个平行过程来研究菱形体边界锐化的机制:细胞分选,即形成边界的“错误”侧的细胞移动到“正确”侧,以及细胞可塑性,即“错误”侧的细胞改变其身份以匹配其周围环境。目的1解决细胞分选的机制,并测试的假设,分选发生在响应2个平行的影响:细胞间的排斥不同的细胞在菱形边界,细胞间的细胞粘附在菱形内的细胞。目的2是解决可塑性的机制。最后,在目标3中,我们考虑了长程信号相互作用以指定特定后脑边界位置的机制。
英文摘要
DESCRIPTION (provided by applicant): The formation of boundaries between or within tissues is a fundamental aspect of animal development. Boundaries function to separate populations of cells with different identities, allowing them to follow independent developmental programs in spite of their close proximity. Additionally, boundaries can form important organizing centers that pattern adjacent cells. In the developing vertebrate central nervous system, boundaries form in an apparently homogeneous neuroepithelium, separating brain regions that subsequently acquire distinct histological and functional properties. In the hindbrain in particular, boundaries form between the rhombomeres, producing a series of 7 segments along the main body axis. In spite of the fundamental importance of boundaries in animal development, surprisingly little is known about the molecules and mechanisms that control boundary formation. Even in Drosophila, where compartment boundaries have intrigued researchers for decades, the actual molecules that mediate boundary formation have only recently begun to be elucidated. The long-term goal of the proposed research is to understand the cellular and molecular basis of rhombomere boundary formation and maintenance during vertebrate hindbrain development. We understand that the appearance of a sharp developmental boundary involves 2 steps: first, long-range signals establish broad domains with distinct regional identities but diffuse boundaries, and secondly fine-scale interactions between cells at the edges of these domains result in the sharpening of the boundaries. In Aims 1 and 2 of this proposal we investigate the mechanisms underlying rhombomere boundary sharpening by studying two parallel processes: cell sorting, whereby cells on the "wrong" side of a forming boundary move to the "right" side, and cell plasticity, whereby cells on the "wrong" side change their identity to match that of their surroundings. Aim 1 addresses the mechanism of cell sorting, and tests the hypothesis that sorting occurs in response to 2 parallel influences: cell-cell repulsion between unlike cells at rhombomere boundaries, and cell-cell adhesion between like cells within rhombomeres. Aim 2 addresses the mechanism of plasticity. Finally, in Aim 3, we consider the mechanism by which long-range signals interact to specify the positions of specific hindbrain boundaries.
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Planar polarity pathway and Nance-Horan syndrome-like 1b have essential cell-autonomous functions in neuronal migration.
平面极性通路和 Nance-Horan 综合征样 1b 在神经元迁移中具有重要的细胞自主功能。
DOI:
10.1242/dev.063842
发表时间:
2011
期刊:
Development (Cambridge, England)
影响因子:
--
作者:
[Walsh,GregoryS, Grant,PaulK, Morgan,JohnA, Moens,CeciliaB]
通讯作者:
Moens,CeciliaB
DOI:
10.1016/j.ydbio.2009.10.029
发表时间:
2010-02-01
期刊:
DEVELOPMENTAL BIOLOGY
影响因子:
2.7
作者:
[Feng, L., Hernandez, R. E., Waxman, J. S., Yelon, D., Moens, C. B.]
通讯作者:
Moens, C. B.
Eph signalling functions downstream of Val to regulate cell sorting and boundary formation in the caudal hindbrain.
Eph 信号在 Val 下游发挥作用,调节后脑尾部的细胞分类和边界形成。
DOI:
10.1242/dev.128.4.571
发表时间:
2001
期刊:
Development (Cambridge, England)
影响因子:
--
作者:
[Cooke,J, Moens,C, Roth,L, Durbin,L, Shiomi,K, Brennan,C, Kimmel,C, Wilson,S, Holder,N]
通讯作者:
Holder,N
DOI:
10.1016/j.ydbio.2008.12.010
发表时间:
2009-03-15
期刊:
DEVELOPMENTAL BIOLOGY
影响因子:
2.7
作者:
[Kemp, Hilary A., Cooke, Julie E., Moens, Cecilia B.]
通讯作者:
Moens, Cecilia B.
DOI:
10.3791/1394
发表时间:
2009-07-17
期刊:
Journal of visualized experiments : JoVE
影响因子:
--
作者:
[Kemp, Hilary A, Carmany-Rampey, Amanda, Moens, Cecilia]
通讯作者:
Moens, Cecilia
共 9 条
Planar cell polarity control of axon guidance
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批准号:10737486
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项目类别:
-
资助金额:$61.62万
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财政年份:2023
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负责人:Cecilia B Moens
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依托单位:
Discovery of sensorimotor connectivity mechanisms in a continuous topographic map
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批准号:10610123
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项目类别:
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资助金额:$24.5万
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财政年份:2022
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负责人:Cecilia B Moens
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依托单位:
Discovery of sensorimotor connectivity mechanisms in a continuous topographic map
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批准号:10557152
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项目类别:
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资助金额:$22.0万
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财政年份:2022
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负责人:Cecilia B Moens
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依托单位:
Discovery of sensorimotor connectivity mechanisms in a continuous topographic map
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批准号:10392177
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项目类别:
-
资助金额:$2.83万
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财政年份:2022
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负责人:Cecilia B Moens
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依托单位:
Topographic mapping by cranial motor neurons
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批准号:10437661
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项目类别:
-
资助金额:$47.98万
-
财政年份:2018
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负责人:Cecilia B Moens
-
依托单位:
Topographic mapping by cranial motor neurons
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批准号:10213152
-
项目类别:
-
资助金额:$20.78万
-
财政年份:2018
-
负责人:Cecilia B Moens
-
依托单位:
Topographic mapping by cranial motor neurons
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批准号:10610122
-
项目类别:
-
资助金额:$27.21万
-
财政年份:2018
-
负责人:Cecilia B Moens
-
依托单位:
Topographic mapping by cranial motor neurons
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批准号:9791356
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项目类别:
-
资助金额:$48.57万
-
财政年份:2018
-
负责人:Cecilia B Moens
-
依托单位:
Mechanisms of Tangential Neuron Migration
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批准号:8639324
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项目类别:
-
资助金额:$39.48万
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财政年份:2013
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负责人:Cecilia B Moens
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依托单位:
Mechanisms of Tangential Neuron Migration
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批准号:9094708
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项目类别:
-
资助金额:$40.32万
-
财政年份:2013
-
负责人:Cecilia B Moens
-
依托单位:
Mechanisms of Tangential Neuron Migration
-
批准号:8719193
-
项目类别:
-
资助金额:$39.0万
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财政年份:2013
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负责人:Cecilia B Moens
-
依托单位:
Mechanisms of Tangential Neuron Migration
-
批准号:9224680
-
项目类别:
-
资助金额:$6.95万
-
财政年份:2013
-
负责人:Cecilia B Moens
-
依托单位:
Identification of genes that regulate electrical synapse formation in vivo
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批准号:8441481
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项目类别:
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资助金额:$25.48万
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财政年份:2012
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负责人:Cecilia B Moens
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依托单位:
Identification of genes that regulate electrical synapse formation in vivo
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批准号:8227420
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项目类别:
-
资助金额:$22.0万
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财政年份:2012
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负责人:Cecilia B Moens
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依托单位:
TILLING the Zebrafish Genome: A Reverse Genetic Approach
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批准号:7498906
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项目类别:
-
资助金额:$70.46万
-
财政年份:2008
-
负责人:Cecilia B Moens
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依托单位:
TILLING the Zebrafish Genome: A Reverse Genetic Approach
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批准号:7915691
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项目类别:
-
资助金额:$69.61万
-
财政年份:2008
-
负责人:Cecilia B Moens
-
依托单位:
INTERACTION OF HUMAN PROFILIN W/PHOSPHATYDILINOSITOL IN GUVS
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批准号:7724052
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项目类别:
-
资助金额:$2.36万
-
财政年份:2008
-
负责人:Cecilia B Moens
-
依托单位:
TILLING the Zebrafish Genome: A Reverse Genetic Approach
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批准号:7685517
-
项目类别:
-
资助金额:$70.3万
-
财政年份:2008
-
负责人:Cecilia B Moens
-
依托单位:
Genetic Mechanisms of Hindbrain Segmentation
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批准号:7232122
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项目类别:
-
资助金额:$29.81万
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财政年份:2005
-
负责人:Cecilia B Moens
-
依托单位:
Genetic Mechanisms of Hindbrain Segmentation
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批准号:7064923
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项目类别:
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资助金额:$30.71万
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财政年份:2005
-
负责人:Cecilia B Moens
-
依托单位:
海外基金