How circuits assemble starting from stem cells is a fundamental question in developmental neurobiology. We test the hypothesis that， in neuronal stem cells， temporal transcription factors predictably control neuronal terminal features and circuit assembly. Using the Drosophila motor system， we manipulate expression of the classic temporal transcription factor Hunchback (Hb) specifically in the NB7-1 stem cell， which produces U motor neurons (MNs)， and then we monitor dendrite morphology and neuromuscular synaptic partnerships. We find that prolonged expression of Hb leads to transient specification of U MN identity， and that embryonic molecular markers do not accurately predict U MN terminal feature... More
How circuits assemble starting from stem cells is a fundamental question in developmental neurobiology. We test the hypothesis that， in neuronal stem cells， temporal transcription factors predictably control neuronal terminal features and circuit assembly. Using the Drosophila motor system， we manipulate expression of the classic temporal transcription factor Hunchback (Hb) specifically in the NB7-1 stem cell， which produces U motor neurons (MNs)， and then we monitor dendrite morphology and neuromuscular synaptic partnerships. We find that prolonged expression of Hb leads to transient specification of U MN identity， and that embryonic molecular markers do not accurately predict U MN terminal features. Nonetheless， our data show Hb acts as a potent regulator of neuromuscular wiring decisions. These data introduce important refinements to current models， show that molecular information acts early in neurogenesis as a switch to control motor circuit wiring， and provide novel insight into the relationship between stem cell and circuit.
