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Drosophila melanogaster: a simple genetic model of kidney structure, function and disease

Journal

NATURE REVIEWS NEPHROLOGY
Volume 18, Issue 7, Pages 417-434

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41581-022-00561-4

Keywords

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Funding

  1. US National Institutes of Health (NIH) [R01-DK092408, U54-DK100227]
  2. Mayo Foundation
  3. Oxalosis & Hyperoxaluria Foundation (OHF)
  4. NIH [P30-DK090728, R25-DK101405]
  5. UK BBSRC
  6. European Commission
  7. Marie Slodowska-Curie Actions

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The fruitfly Drosophila melanogaster serves as a suitable and cost-effective model for studying kidney diseases. It has advantages such as easy maintenance, availability of genetic mutants and powerful transgenic technologies. Various tissues in Drosophila melanogaster are involved in renal and excretory functions, allowing investigation of epithelial transport, kidney stone formation, and diseases associated with specific genes. The fly model provides insights into the mechanisms of kidney disease.
Although the genetic basis of many kidney diseases is being rapidly elucidated, their experimental study remains problematic owing to the lack of suitable models. The fruitfly Drosophila melanogaster provides a rapid, ethical and cost-effective model system of the kidney. The unique advantages of D. melanogaster include ease and low cost of maintenance, comprehensive availability of genetic mutants and powerful transgenic technologies, and less onerous regulation, as compared with mammalian systems. Renal and excretory functions in D. melanogaster reside in three main tissues - the transporting renal (Malpighian) tubules, the reabsorptive hindgut and the endocytic nephrocytes. Tubules contain multiple cell types and regions and generate a primary urine by transcellular transport rather than filtration, which is then subjected to selective reabsorption in the hindgut. By contrast, the nephrocytes are specialized for uptake of macromolecules and equipped with a filtering slit diaphragm resembling that of podocytes. Many genes with key roles in the human kidney have D. melanogaster orthologues that are enriched and functionally relevant in fly renal tissues. This similarity has allowed investigations of epithelial transport, kidney stone formation and podocyte and proximal tubule function. Furthermore, a range of unique quantitative phenotypes are available to measure function in both wild type and disease-modelling flies. Drosophila melanogaster can be a useful experimental model in nephrology. Here, the authors examine the fly renal system, focusing on the Malpighian tubules and nephrocytes, and discuss its advantages and limitations as a model system and the mechanistic insights into kidney disease that they have provided.

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