4.4 Article

Methods for analyzing neuronal structure and activity in Caenorhabditis elegans

期刊

GENETICS
卷 218, 期 4, 页码 -

出版社

GENETICS SOCIETY AMERICA
DOI: 10.1093/genetics/iyab072

关键词

synapse, connectome; Ca2+-imaging; fluorescent reporter gene; graph theory; nervous system; nematode; WormBook

资金

  1. NIH [R01GM066897, 5T32DK7328-37, 5T32DK007328-35, 5T32MH015174-38, 5T32MH015174-37]
  2. G. Harold and Leila Y. Mathers Charitable Foundation
  3. University of Vienna
  4. Research Institute of Molecular Pathology (IMP)
  5. Simons Foundation [543069]
  6. International Research Scholar Program by the Wellcome Trust [208565/Z/17/Z]
  7. Howard Hughes Medical Institute [208565/Z/17/Z]
  8. Boehringer Ingelheim
  9. Wellcome Trust [208565/Z/17/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

The Caenorhabditis elegans model organism with its unique properties is advantageous for studying the nervous system. With advanced techniques and fluorescent probes, visualization and identification of neurons in this transparent animal are possible, enabling efficient research on nervous system structure and function. Recent developments in microscopy and fluorescent reporters sensitive to Ca2+ levels have further enhanced the study of neuron activity across the entire nervous system.
The model research animal Caenorhabditis elegans has unique properties making it particularly advantageous for studies of the nervous system. The nervous system is composed of a stereotyped complement of neurons connected in a consistent manner. Here, we describe methods for studying nervous system structure and function. The transparency of the animal makes it possible to visualize and identify neurons in living animals with fluorescent probes. These methods have been recently enhanced for the efficient use of neuron-specific reporter genes. Because of its simple structure, for a number of years, C. elegans has been at the forefront of connectomic studies defining synaptic connectivity by electron microscopy. This field is burgeoning with new, more powerful techniques, and recommended up-to-date methods are here described that encourage the possibility of new work in C. elegans. Fluorescent probes for single synapses and synaptic connections have allowed verification of the EM reconstructions and for experimental approaches to synapse formation. Advances in microscopy and in fluorescent reporters sensitive to Ca2+ levels have opened the way to observing activity within single neurons across the entire nervous system.

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