COOKIES: By using this website you agree that we can place Google Analytics Cookies on your device for performance monitoring. |
University of Cambridge > Talks.cam > MRC LMB Neurobiology Seminars > Genetic analysis of layer specific axon targeting in the Drosophila visual system
Genetic analysis of layer specific axon targeting in the Drosophila visual systemAdd to your list(s) Download to your calendar using vCal
If you have a question about this talk, please contact Greg Jefferis. The segregation of axon and dendrite projections into distinct synaptic layers is a fundamental principle of nervous system organization and the structural basis for information processing in the brain1. Layer-specific recognition molecules that allow projecting neurons to stabilize transient contacts and initiate synaptogenesis2, 3 have been identified. However, most of the neuronal cell-surface molecules critical for layer organization are expressed broadly in the developing nervous system4, 5, raising the question of how these so-called permissive adhesion molecules support synaptic specificity. Here we show that the temporal expression dynamics of the zinc-finger protein sequoia is the major determinant of Drosophila photoreceptor connectivity into distinct synaptic layers. Neighbouring R8 and R7 photoreceptors show consecutive peaks of elevated sequoia expression, which correspond to their sequential target-layer innervation. Loss of sequoia in R7 leads to a projection switch into the R8 recipient layer, whereas a prolonged expression in R8 induces a redirection of their axons into the R7 layer. The sequoia-induced axon targeting is mediated through the ubiquitously expressed Cadherin-N cell adhesion molecule. Our data support a model in which recognition specificity during synaptic layer formation is generated through a temporally restricted axonal competence to respond to broadly expressed adhesion molecules. Because developing neurons innervating the same target area often project in a distinct, birth-order-dependent sequence, temporal identity seems to contain crucial information in generating not only cell type diversity during neuronal division6 but also connection diversity of projecting neurons. See also: http://www.nature.com/nature/journal/vaop/ncurrent/abs/nature07407.html This talk is part of the MRC LMB Neurobiology Seminars series. This talk is included in these lists:
Note that ex-directory lists are not shown. |
Other listsGraphene CDT Advanced Technology Lectures Collaboration Events Danby SocietyOther talks'Ways of Reading, Looking, and Imagining: Contemporary Fiction and Its Optics' Regulatory principles in human development and evolution Graph Convolutional Networks for Natural Language Processing and Relational Modeling Frontiers in paediatric cancer research Taking Investment in Education Seriously - Two Part Series The Beginning of Our Universe and what we don't know about Physics Understanding mechanisms and targets of malaria immunity to advance vaccine development Lunchtime Talk: Helen's Bedroom mTORC1 signaling coordinates different POMC neurons subpopulations to regulate feeding Stereodivergent Catalysis, Strategies and Tactics Towards Secondary Metabolites as enabling tools for the Study of Natural Products Biology Molecular mechanisms of cardiomyopathies in patients with severe non-ischemic heart failure Access to Medicines |