| Literature DB >> 35147953 |
Jeff Hardin1, Joel Serre2, Ryan King3, Elise Walck-Shannon4, David Reiner5.
Abstract
The Caenorhabditis elegans embryo is well suited for analysis of directed cell rearrangement via modern microscopy, due to its simple organization, short generation time, transparency, invariant lineage, and the ability to generate engineered embryos expressing various fluorescent proteins. This chapter provides an overview of routine microscopy techniques for imaging dorsal intercalation, a convergent extension-like morphogenetic movement in the embryonic epidermis of C. elegans, including making agar mounts, low-cost four-dimensional (4D) Nomarski microscopy, laser microsurgery, and 4D fluorescence microscopy using actin and junctional fusion proteins, as well as tissue-specific promoters useful for studying dorsal intercalation.Entities:
Keywords: C. elegans; Cell intercalation; Convergent extension; Epidermis; Morphogenesis
Mesh:
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Year: 2022 PMID: 35147953 PMCID: PMC9528972 DOI: 10.1007/978-1-0716-2035-9_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745