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Xgr is involved in body size control in Drosophila through promoting glucose uptake in the Malpighian tubules

doi: 10.1016/j.jgg.2025.05.007
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to Dr. Suning Liu for AMPK-T184D flies. This study was funded by the National Key R&D Program of China (2021YFA0805800, 2023YFE0107700, and 2020YFA0803202 to R.J.), the 111 Project (D18010 to R.J.), the Guangzhou Medical University Discipline Construction Funds (Basic Medicine) (JCXKJS2022A02 to R.J.), Guangdong Basic and Applied Basic Research Foundation (2024A1515010752 to C.W.), and the Special Innovation Projects of Universities in Guangdong Province (2022KTSCX096 to C.W.). Thanks to the Jiao lab members for stimulating discussions.

We thank the BDSC, VDRC, THFC, and GDRC for providing fly stocks. We are grateful to Dr. Hai Huang for ATP-SPARK and AMPK-SPARK flies

  • Received Date: 2025-03-01
  • Accepted Date: 2025-05-15
  • Rev Recd Date: 2025-05-15
  • Available Online: 2025-07-11
  • Body size control is fundamental to development and requires proper energy engagement. One of the key energy sensing factors is AMP-activated protein kinase (AMPK), which regulates glucose uptake to ensure ATP production and nutrition supply during development. Here, we identify that the mutation of xgr, a gene encoding an ATPase, results in a reduced body size in Drosophila. Xgr is primarily expressed in the epithelial cells of the Malpighian tubules and the midguts. Loss of xgr leads to the inactivation of the AMPK signaling due to an increased ATP level. Glucose reabsorption in the Malpighian tubules is significantly reduced, as the Glut1 translocation to the plasma membrane is significantly disrupted in the absence of Xgr function. Our results suggest that Xgr function in the Malpighian tubules is essential to systemic glucose supply and energy homeostasis at the organismal level, thereby impacting body size. Our findings provide a mechanistic connection between energy homeostasis and animal size control during development.

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      沈阳化工大学材料科学与工程学院 沈阳 110142

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