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. 2021 Oct 28;10(10):bio058812. doi: 10.1242/bio.058812

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© 2021. Published by The Company of Biologists Ltd

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Fig. 6. — Loss of dynein heavy chain in Dnaaf3 mutant motile cilia. Immunofluorescence imaging of chordotonal neurons in pupal antenna; Dnah5 protein (green) and phalloidin staining of F-actin (red), which marks the scolopale structures surrounding the ciliary dendrites. (A) Dnaaf3^ΔCR heterozygote showing Dnah5 protein in cell bodies (cb) and cilia (ci). (B) Dnaaf3^ΔCR homozygote showing Dnah5 in cell bodies and dendrite inner segments (is) but absent from cilia. (A′,B′) Corresponding Dnah5 channels only. Number of antennae imaged: heterozygote n=15; homozygote n=10. Scale bars: 5 µm.