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Alliance"],"published-print":{"date-parts":[[2023,7]]},"abstract":"<jats:p>\n                    In age-related neurodegenerative diseases, like Alzheimer\u2019s and Parkinson\u2019s, disease-specific proteins become aggregation-prone and form amyloid-like deposits. Depletion of SERF proteins ameliorates this toxic process in worm and human cell models for diseases. Whether SERF modifies amyloid pathology in mammalian brain, however, has remained unknown. Here, we generated conditional\n                    <jats:italic>Serf2<\/jats:italic>\n                    knockout mice and found that full-body deletion of\n                    <jats:italic>Serf2<\/jats:italic>\n                    delayed embryonic development, causing premature birth and perinatal lethality. Brain-specific\n                    <jats:italic>Serf2<\/jats:italic>\n                    knockout mice, on the other hand, were viable, and showed no major behavioral or cognitive abnormalities. In a mouse model for amyloid-\u03b2 aggregation, brain depletion of\n                    <jats:italic>Serf2<\/jats:italic>\n                    altered the binding of structure-specific amyloid dyes, previously used to distinguish amyloid polymorphisms in the human brain. These results suggest that\n                    <jats:italic>Serf2<\/jats:italic>\n                    depletion changed the structure of amyloid deposits, which was further supported by scanning transmission electron microscopy, but further study will be required to confirm this observation. Altogether, our data reveal the pleiotropic functions of SERF2 in embryonic development and in the brain and support the existence of modifying factors of amyloid deposition in mammalian brain, which offer possibilities for polymorphism-based interventions.\n                  <\/jats:p>","DOI":"10.26508\/lsa.202201730","type":"journal-article","created":{"date-parts":[[2023,5,2]],"date-time":"2023-05-02T13:25:41Z","timestamp":1683033941000},"page":"e202201730","update-policy":"https:\/\/doi.org\/10.26508\/lsa.crossmarkpolicy","source":"Crossref","is-referenced-by-count":10,"title":["Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain"],"prefix":"10.26508","volume":"6","author":[{"given":"Esther","family":"Stroo","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03cv38k47","id-type":"ROR","asserted-by":"publisher"}],"name":"European Research Institute for the Biology of Ageing, University of Groningen, University 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