Differential expression of antioxidant system genes in honey bee (Apis mellifera L.) caste development mitigates ROS-mediated oxidative damage in queen larvae.
Douglas Elias SantosAnderson de Oliveira SouzaGustavo Jacomini TibérioLuciane Carla AlbericiKlaus HartfelderPublished in: Genetics and molecular biology (2020)
The expression of morphological differences between the castes of social bees is triggered by dietary regimes that differentially activate nutrient-sensing pathways and the endocrine system, resulting in differential gene expression during larval development. In the honey bee, Apis mellifera, mitochondrial activity in the larval fat body has been postulated as a link that integrates nutrient-sensing via hypoxia signaling. To understand regulatory mechanisms in this link, we measured reactive oxygen species (ROS) levels, oxidative damage to proteins, the cellular redox environment, and the expression of genes encoding antioxidant factors in the fat body of queen and worker larvae. Despite higher mean H2O2 levels in queens, there were no differences in ROS-mediated protein carboxylation levels between the two castes. This can be explained by their higher expression of antioxidant genes (MnSOD, CuZnSOD, catalase, and Gst1) and the lower ratio between reduced and oxidized glutathione (GSH/GSSG). In worker larvae, the GSG/GSSH ratio is elevated and antioxidant gene expression is delayed. Hence, the higher ROS production resulting from the higher respiratory metabolism in queen larvae is effectively counterbalanced by the up-regulation of antioxidant genes, avoiding oxidative damage. In contrast, the delay in antioxidant gene expression in worker larvae may explain their endogenous hypoxia response.
Keyphrases
- gene expression
- reactive oxygen species
- oxidative stress
- aedes aegypti
- anti inflammatory
- drosophila melanogaster
- poor prognosis
- genome wide
- dna damage
- dna methylation
- cell death
- adipose tissue
- genome wide identification
- binding protein
- endothelial cells
- healthcare
- magnetic resonance imaging
- transcription factor
- genome wide analysis
- small molecule
- radiation induced
- contrast enhanced