MassIVE MSV000091235

Partial Public PXD040008

Overexpression of the citrate transporters SLC13A5 and SLC25A1 in the mouse elicit different metabolic responses and phenotypes

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Description

Cytosolic citrate is imported from the mitochondria by SLC25A1, and from the extracellular milieu by SLC13A5. In the cytosol, citrate is used by ACLY to generate acetyl-CoA, which can then be exported to the endoplasmic reticulum (ER) by SLC33A1. Here, we report the generation of mice with systemic overexpression (sTg) of SLC25A1 or SLC13A5. Both animals displayed increased cytosolic levels of citrate and acetyl-CoA; however, SLC13A5 sTg mice developed a progeria-like phenotype with premature death, while SLC25A1 sTg mice did not. Analysis of the metabolic profile revealed widespread differences. Furthermore, SLC13A5 sTg mice displayed increased engagement of the ER acetylation machinery through SLC33A1, while SLC25A1 sTg mice did not. In conclusion, our findings point to different biological responses to SLC13A5- or SLC25A1-mediated import of citrate and suggest that the directionality of the citrate/acetyl-CoA pathway can transduce different signals. Results uploaded here in MassIVE are acetyl-proteomics studies of the livers of SLC13A5 and SLC25A1 mice as compared to their WT litter-mates. [doi:10.25345/C56W96K2T] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Acetylation ; Proteomics ; Subcellular

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Principal Investigators:
(in alphabetical order) 		John Denu, University of Wisconsin - Madison, United States
Submitting User: alawton2
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