A major challenge in neuroscience is to comprehend how differentiating embryonic cells fashion de novo the working circuits and networks that make up a nervous system. We propose WormGUIDES, a resource that would facilitate understanding the cellular origins of an entire nervous system from all angles?cell birth, migration and differentiation; neurite formation, targeted outgrowth and bundling; and ultimately, synapse formation and tuning of functional circuits?with single cell resolution, from conception until hatching. Building on the innovations we established in the first funding cycle, we propose to use ShootingStar, a novel platform for real-time cell tracking and optical manipulation to label single neurons, and isotropic high-resolution diSPIM imaging to capture nerve bundling dynamics and single cell outgrowth in the early developing embryo when the major architecture of the nervous system is constructed. We will also assign all nuclear identities and positions from the first cell division until hatching. Finally, we will share the knowledge with the community through WormGUIDES Atlas software, displaying models, supporting images and primary data. Completion of the WormGUIDES resource will ultimately complement the existing cell lineage, adult nervous system structure, and collective genomic and genetic data for the worm, creating a fourth pillar of systems-level knowledge that will enhance our understanding of neurodevelopment.

Public Health Relevance

C. elegans has been a key animal model for understanding a broad spectrum of human diseases. We propose WormGUIDES, a novel systems-level resource that will facilitate examination of cellular decisions in the developing nervous system of this nematode, enhancing the value of C. elegans as a model organism and resulting in new insights in development, neuroscience and disease.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Resource-Related Research Projects (R24)
Project #
3R24OD016474-05S1
Application #
9627012
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Zou, Sige
Project Start
2013-06-13
Project End
2021-05-31
Budget Start
2018-02-01
Budget End
2018-05-31
Support Year
5
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Yale University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
Katzman, Braden; Tang, Doris; Santella, Anthony et al. (2018) AceTree: a major update and case study in the long term maintenance of open-source scientific software. BMC Bioinformatics 19:121
Shah, Pavak Kirit; Santella, Anthony; Jacobo, Adrian et al. (2017) An In Toto Approach to Dissecting Cellular Interactions in Complex Tissues. Dev Cell 43:530-540.e4
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Santella, Anthony; Kovacevic, Ismar; Herndon, Laura A et al. (2016) Digital development: a database of cell lineage differentiation in C. elegans with lineage phenotypes, cell-specific gene functions and a multiscale model. Nucleic Acids Res 44:D781-5
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Stavoe, Andrea K H; Hill, Sarah E; Hall, David H et al. (2016) KIF1A/UNC-104 Transports ATG-9 to Regulate Neurodevelopment and Autophagy at Synapses. Dev Cell 38:171-85
Santella, Anthony; Catena, Raúl; Kovacevic, Ismar et al. (2015) WormGUIDES: an interactive single cell developmental atlas and tool for collaborative multidimensional data exploration. BMC Bioinformatics 16:189
Vidal, Berta; Santella, Anthony; Serrano-Saiz, Esther et al. (2015) C. elegans SoxB genes are dispensable for embryonic neurogenesis but required for terminal differentiation of specific neuron types. Development 142:2464-77

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