Genetic Analysis of Dendritic Targeting
Genetic Analysis of Dendritic Targeting
批准号:
6442032
负责人:
Lawrence S. Goldstein
金额:
$3.4万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-12-14 至 2004-11-30
关键词:
Drosophilidae India acetylcholine arthropod genetics axon cell sorting chimeric proteins confocal scanning microscopy cooperative study dendrites epithelium gene targeting green fluorescent proteins intracellular transport mutant neural information processing neurons neurophysiology nicotinic receptors protein localization synapses tissue /cell culture transferrin receptor video microscopy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant)
Like polarized epithelial cells, neurons are divided into two functionally
distinct compartments and the axon and dendrites of a neuron performs
distinctly different functions. Considerable work has established the existence
of additional distinct sets of proteins that are selectively partitioned into
these compartments. It is obvious that localization of these proteins is
critical for proper functioning of the cell and the flow of information in the
nervous system. Intuitively such a process should require a sorting system to
identify the proteins for a certain intracellular destinations like the
dendritic compartment, a transport machine to carry them, and finally, a
mechanism that will retain the proteins in their respective place of action.
This is an important problem in contemporary Cellular Neurobiology in which
mechanistic understanding is quite limited. The goal of this collaborative
project is to identify genes needed for preferential sorting of proteins and
vesicles to the dendritic compartment of neurons. In order to achieve the
stated objective, a live assay for dendritic sorting and transport will be
developed in Drosophila using the green fluorescent protein (GFP) tagged
tranferrin receptor (TfR) and the Drosophila homologues (ARD, ALS) of the
a-subunit of nicotinic acetylcholine receptor (nAChR) proteins. These GFP
tagged proteins will be expressed in the embryonic and larval nervous system
and their subcellular localization will be characterized in both the live and
fixed tissue preparations. An epifluorescence video microscopic set up as well
as the confocal microscopic techniques will be used to observe this sorting
process. Once established the assay will be used to characterize various known
mutants of the fly genome and also to screen for new mutants that will affect
the dendritic targeting of TfR/ARD/ALS-GFP proteins. It is expected that, at
the end of a three-year period, these experiments will yield a list of
candidate proteins involved in the dendritic sorting of TfR, ARD and ALS in
Drosophila. In addition, it will also establish a genetically testable cellular
assay system for dendritic protein sorting in live animal models. The proposed
project will be executed in collaboration with Dr. Krishanu Ray at TIFR, India,
and the research will be done primarily in India as an extension of NIH grant #
ROl GM 35252.
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