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Updated: Apr 19, 2026

An Anoxia-starvation Model for Ischemia/Reperfusion in C. elegans
Published on: March 11, 2014
A role for peroxidasin PXN-1 in aspects of C. elegans development
Juyeon Lee1, Jaya Bandyopadhyay2, Jin Il Lee3
1Department of Life Science, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Abstract:
The Caenorhabditis elegans peroxidasins, PXN-1 and PXN-2, are extracellular peroxidases; pxn-2 is involved in muscle-epidermal attachment during embryonic morphogenesis and in specific axon guidance. Here we investigate potential roles of the other homologue of peroxidasin, pxn-1, in C. elegans. A pxn-1 deletion mutant showed high lethality under heat-stress conditions. Using a transcriptional GFP reporter, pxn-1 expression was observed in various tissues including neurons, muscles, and hypodermis. A translational fusion showed that PXN-1::GFP was secreted and localized in extracellular matrix, particularly along body wall muscles and pharyngeal muscles. Various neuronal developmental defects were observed in pxn-1 mutants and in pxn-1 over-expressing animals, including handedness, branching, breakage, tangling, and defasciculation. These results suggest that pxn-1, like other peroxidasins, plays an important role throughout development.
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