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However, the molecular mechanism(s) underlying GSAP-dependent pathogenesis remains largely elusive. Here, through unbiased proteomics and single-nuclei RNAseq, we identified that GSAP regulates multiple biological pathways, including protein phosphorylation, trafficking, lipid metabolism, and mitochondrial function. We demonstrated that GSAP physically interacts with the Fe65\u2013APP complex to regulate APP trafficking\/partitioning. GSAP is enriched in the mitochondria-associated membrane (MAM) and regulates lipid homeostasis through the amyloidogenic processing of APP. GSAP deletion generates a lipid environment unfavorable for AD pathogenesis, leading to improved mitochondrial function and the rescue of cognitive deficits in an AD mouse model. Finally, we identified a novel GSAP single-nucleotide polymorphism that regulates its brain transcript level and is associated with an increased AD risk. Together, our findings indicate that GSAP impairs mitochondrial function through its MAM localization and that lowering GSAP expression reduces pathological effects associated with AD.<\/jats:p>","DOI":"10.1084\/jem.20202446","type":"journal-article","created":{"date-parts":[[2021,5,27]],"date-time":"2021-05-27T02:21:36Z","timestamp":1622082096000},"update-policy":"https:\/\/doi.org\/10.1084\/jem.crossmarkpolicy","source":"Crossref","is-referenced-by-count":32,"title":["GSAP regulates lipid homeostasis and mitochondrial function associated with Alzheimer\u2019s disease"],"prefix":"10.1084","volume":"218","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5197-9560","authenticated-orcid":true,"given":"Peng","family":"Xu","sequence":"first","affiliation":[{"name":"Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, NY 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