A novel adipose loss-of-function mutant in Drosophila .

Autor: Losurdo NA; Department of Neurobiology, University of Utah, Salt Lake, UT, USA., Bibo A; Department of Neurobiology, University of Utah, Salt Lake, UT, USA., Bedke J; Department of Neurobiology, University of Utah, Salt Lake, UT, USA., Link N; Department of Neurobiology, University of Utah, Salt Lake, UT, USA.
Jazyk: angličtina
Zdroj: Fly [Fly (Austin)] 2024 Dec; Vol. 18 (1), pp. 2352938. Date of Electronic Publication: 2024 May 13.
DOI: 10.1080/19336934.2024.2352938
Abstrakt: To identify genes required for brain growth, we took an RNAi knockdown reverse genetic approach in Drosophila . One potential candidate isolated from this effort is the anti-lipogenic gene adipose ( adp ). Adp has an established role in the negative regulation of lipogenesis in the fat body of the fly and adipose tissue in mammals. While fat is key to proper development in general, adp has not been investigated during brain development. Here, we found that RNAi knockdown of adp in neuronal stem cells and neurons results in reduced brain lobe volume and sought to replicate this with a mutant fly. We generated a novel adp mutant that acts as a loss-of-function mutant based on buoyancy assay results. We found that despite a change in fat content in the body overall and a decrease in the number of larger (>5 µm) brain lipid droplets, there was no change in the brain lobe volume of mutant larvae. Overall, our work describes a novel adp mutant that can functionally replace the long-standing adp 60 mutant and shows that the adp gene has no obvious involvement in brain growth.
Databáze: MEDLINE