Untwisting the Caenorhabditis elegans embryo

Author:

Christensen Ryan Patrick1,Bokinsky Alexandra2,Santella Anthony3,Wu Yicong1,Marquina-Solis Javier4,Guo Min15,Kovacevic Ismar3,Kumar Abhishek14,Winter Peter W1,Tashakkori Nicole1,McCreedy Evan2,Liu Huafeng5,McAuliffe Matthew2,Mohler William6,Colón-Ramos Daniel A4,Bao Zhirong3,Shroff Hari1

Affiliation:

1. Section on High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, United States

2. Biomedical Imaging Research Services Section, Center for Information Technology, National Institutes of Health, Bethesda, United States

3. Developmental Biology Program, Sloan-Kettering Institute, New York, United States

4. Program in Cellular Neuroscience, Neurodegeneration and Repair, Department of Cell Biology, Yale University School of Medicine, New Haven, United States

5. State Key Laboratory of Modern Optical Instrumentation, College of Optical Science and Engineering, Zhejiang University, Hangzhou, China

6. Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, United States

Abstract

The nematode Caenorhabditis elegans possesses a simple embryonic nervous system with few enough neurons that the growth of each cell could be followed to provide a systems-level view of development. However, studies of single cell development have largely been conducted in fixed or pre-twitching live embryos, because of technical difficulties associated with embryo movement in late embryogenesis. We present open-source untwisting and annotation software (http://mipav.cit.nih.gov/plugin_jws/mipav_worm_plugin.php) that allows the investigation of neurodevelopmental events in late embryogenesis and apply it to track the 3D positions of seam cell nuclei, neurons, and neurites in multiple elongating embryos. We also provide a tutorial describing how to use the software (<xref ref-type="supplementary-material" rid="SD1-data">Supplementary file 1</xref>) and a detailed description of the untwisting algorithm (Appendix). The detailed positional information we obtained enabled us to develop a composite model showing movement of these cells and neurites in an 'average' worm embryo. The untwisting and cell tracking capabilities of our method provide a foundation on which to catalog C. elegans neurodevelopment, allowing interrogation of developmental events in previously inaccessible periods of embryogenesis.

Funder

National Institute of Biomedical Imaging and Bioengineering

Center for Information Technology

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Marine Biological Laboratory

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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