Abstract
The Drosophila embryonic ventral epidermis has served as a unique tissue for the genetic analysis of patterning. Two types of epidermal cells are easily distinguished: those that secrete short, thick hair-like structures called denticles and cells that only secrete smooth cuticle. Denticle-secreting cells form segmentally repeated belts. Within each belt, six types of denticles can be recognized according to size, shape, and orientation (types 1–6). They are arranged in a stereotypical manner within each denticle belt. This pattern results from the spatially organized activation of several signaling pathways during embryogenesis. Cuticle patterns therefore provide a sensitive readout of signaling activity and other patterning mechanisms. Here, I describe methods of preparation and analysis of cuticles from 1st instar larvae as well as from 3rd instar larvae. In addition, a protocol to simultaneously analyze cuticles and β-galactosidase activity of embryos expressing lacZ reporter genes is presented.
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References
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© 2008 Humana Press Inc., Totowa, NJ
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Alexandre, C. (2008). Cuticle Preparation of Drosophila Embryos and Larvae. In: Dahmann, C. (eds) Drosophila. Methods in Molecular Biology, vol 420. Humana Press. https://doi.org/10.1007/978-1-59745-583-1_11
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DOI: https://doi.org/10.1007/978-1-59745-583-1_11
Publisher Name: Humana Press
Print ISBN: 978-1-58829-817-1
Online ISBN: 978-1-59745-583-1
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