1. The role ofPeroxin 7duringDrosophilaembryonic development
- Author
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C Pridie and Andrew J. Simmonds
- Subjects
0301 basic medicine ,chemistry.chemical_classification ,Reactive oxygen species ,biology ,fungi ,Embryogenesis ,Peroxin ,General Medicine ,Peroxisome ,biology.organism_classification ,Cell biology ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,chemistry ,Organelle ,Genetics ,Drosophila melanogaster ,Molecular Biology ,030217 neurology & neurosurgery ,Biogenesis ,Biotechnology - Abstract
Peroxisomes are organelles in eukaryotic cells responsible for processing several types of lipids and management of reactive oxygen species. A conserved family of peroxisome biogenesis (Peroxin, Pex) genes encode proteins essential to peroxisome biogenesis or function. In yeast and mammals, PEROXIN7 (PEX7) acts as a cytosolic receptor protein that targets enzymes containing a peroxisome targeting signal 2 (PTS2) motif for peroxisome matrix import. The PTS2 motif is not present in the Drosophila melanogaster homologs of these enzymes. However, the fly genome contains a Pex7 gene (CG6486) that is very similar to yeast and human PEX7. We find that Pex7 is expressed in tissue-specific patterns analogous to differentiating neuroblasts in D. melanogaster embryos. This is correlated with a requirement for Pex7 in this cell lineage as targeted somatic Pex7 knockout in embryonic neuroblasts reduced survival. We also found that Pex7 over-expression in the same cell lineages caused lethality during the larval stage. Targeted somatic over-expression of a Pex7 transgene in neuroblasts of Pex7 homozygous null mutants resulted in a semi-lethal phenotype similar to targeted Pex7 knockout. These findings suggest that D. melanogaster has tissue-specific requirements for Pex7 during embryo development.
- Published
- 2021
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