Nerve-derived trophic factors and DNA elements controlling expression of genes encoding synaptic proteins in skeletal muscle fibers

• Published in: Canadian journal of applied physiology Vol. 23; no. 4; p. 366
• Main Authors: Jasmin, B J, Gramolini, A O, Adatia, F A, Angus, L, Boudreau-Larivière, C, Chan, R Y, Krupa, A M, Lunde, J A, Mankal, F A, Wu, J
• Format: Journal Article
• Language: English
• Published: United States 01.08.1998
• Subjects: Cell Nucleus - metabolism; DNA - genetics; Gene Expression Regulation; Humans; Motor Neurons - physiology; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - metabolism; Nerve Growth Factors - physiology; Nerve Tissue Proteins - genetics; Neuromuscular Junction - metabolism; Neuronal Plasticity - physiology; Receptors, Presynaptic - physiology; Second Messenger Systems - physiology; Signal Transduction - physiology; Synapses - metabolism; Synapses - physiology; Synaptic Membranes - metabolism; Synaptic Membranes - ultrastructure; Transcription, Genetic
• DOI: 10.1139/h98-021
• ISSN: 1066-7814

The neuromuscular junction represents an excellent model system for studying various critical issues in neurobiology at the molecular, cellular, and physiological levels. Our understanding of the basic events underlying synpase formation, maintenance, and plasticity has progressed considerably over the last few years primarily because of the numerous studies that have focused on this synapse and used sophisticated recombinant DNA technology. Recent data indicate that myonuclei located in the vicinity of the postsynaptic membrane are in a differential state of transcription compared to nuclei of the extrasynaptic sarcoplasm. Thus, renewal of postsynaptic membrane proteins appears to occur via a mechanism involving the local transcriptional activation of genes encoding these specialized proteins and extracellular cues originating from motoneurons. Such interaction between presynaptic nerve terminals and the postsynaptic sarcoplasm indicates that the entire signal transduction pathway is compartmentalized at the level of the neuromuscular junction. Expression of these genes appears less coregulated than originally anticipated, indicating that maintenance of the postsynaptic membrane requires the contribution of multiple extracellular signals, which ultimately urge target transcription factors to distinct DNA regulatory elements via various second messenger systems.