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http://hdl.handle.net/10603/428987
Title: | Roles of Drosophila Beadex and CG9650 in the development and functioning of the larval neuromuscular junctions |
Researcher: | Chitre, Kripa |
Guide(s): | Nongthomba, Upendra |
Keywords: | Genetics and Heredity Life Sciences Molecular Biology and Genetics |
University: | Indian Institute of Science Bangalore |
Completed Date: | 2021 |
Abstract: | In eukaryotes, all voluntary and involuntary actions like, cognition, learning and memory, voluntary movements, feeding, etc., are coordinated by the employment of neuronal circuitry that transmits the signal from the source (in the central nervous system) to an effector (another neuron, tissue or organ). Neurotransmission, a process in which neurotransmitters released by axon terminals of a neuron binds to receptors on dendrites of another neuron, or other effector tissue or organ, is indispensably responsible for these actions. Many voluntary actions, like locomotion, result from chemical synapses that are formed between a motor neuron and a skeletal muscle, which are also known as neuromuscular junctions (NMJ). Along with appropriate growth and accurate organization, a functional NMJ demands a well balanced expression of molecular effectors for robust synaptic transmission. Several signaling pathways, including the Wnt pathway, BMP pathway, MAPK pathway, and Syt4 underly the formation and maintenance of a functional NMJ. Many of the signaling molecules involved in these pathways regulate various morphological features of the NMJ like the span area, branch length, bouton numbers and size, as well as the physiology at the synapse. Drosophila larval neurons have been used extensively as a model to identify new molecular players and decode neuronal circuits involved. Extensive work in Drosophila larval NMJ led to the identification of major molecular players and their developmental and functional roles, like endocytosis e.g. by studies on shibire (dynamin), exocytosis by studies on cacophony (calcium ion channel), SNARE proteins (for synaptic vesicle fusion), etc., regulators of NMJ morphology, like highwire, futsch, TDP-43, Rae1, Dishelved, LIMK1, etc., active zone assembly players BRP, Syd-1 (RhoGAP100F), Lipirin-and#945;., etc. Though these studies have proven to be valuable paradigms to study the mammalian synapses, many new molecular candidates whose function and interactions at the NMJ remain uncovered... |
Pagination: | 128 |
URI: | http://hdl.handle.net/10603/428987 |
Appears in Departments: | Molecular Reproduction Development and Genetics |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 71.89 kB | Adobe PDF | View/Open |
02_prelim pages.pdf | 336.24 kB | Adobe PDF | View/Open | |
03_table of contents.pdf | 131.13 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 78.98 kB | Adobe PDF | View/Open | |
05_chapter 1.pdf | 1.01 MB | Adobe PDF | View/Open | |
06_chapter 2.pdf | 172.3 kB | Adobe PDF | View/Open | |
07_chapter 3.pdf | 2.76 MB | Adobe PDF | View/Open | |
08_chapter 4.pdf | 900.12 kB | Adobe PDF | View/Open | |
11_annexure.pdf | 207 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 147.44 kB | Adobe PDF | View/Open |
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