Please use this identifier to cite or link to this item: 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

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02_prelim pages.pdf336.24 kBAdobe PDFView/Open
03_table of contents.pdf131.13 kBAdobe PDFView/Open
04_abstract.pdf78.98 kBAdobe PDFView/Open
05_chapter 1.pdf1.01 MBAdobe PDFView/Open
06_chapter 2.pdf172.3 kBAdobe PDFView/Open
07_chapter 3.pdf2.76 MBAdobe PDFView/Open
08_chapter 4.pdf900.12 kBAdobe PDFView/Open
11_annexure.pdf207 kBAdobe PDFView/Open
80_recommendation.pdf147.44 kBAdobe PDFView/Open
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