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dc.contributor.authorLambropoulos, Nicholas
dc.contributor.authorGarcia, Alvaro
dc.contributor.authorClarke, Ronald J.
dc.date.accessioned2019-09-10
dc.date.available2019-09-10
dc.date.issued2015-12-29
dc.identifier.citationLambropoulos, N., Garcia, A., & Clarke, R. J. (2015). Stimulation of Na+,K+-ATPase Activity as a Possible Driving Force in Cholesterol Evolution. The Journal of Membrane Biology, 249(3), 251–259. https://doi.org/10.1007/s00232-015-9864-zen
dc.identifier.urihttp://hdl.handle.net/2123/21064
dc.description.abstractCholesterol is exclusively produced by animals and is present in the plasma membrane of all animal cells. In contrast, the membranes of fungi and plants contain other sterols. To explain the exclusive preference of animal cells for cholesterol we propose that cholesterol may have evolved to optimise the activity of a crucial protein found in the plasma membrane of all multicellular animals, namely the Na+,K+-ATPase. To test this hypothesis mirror tree and phylogenetic distribution analyses have been conducted of the Na+,K+-ATPase and 3β-hydroxysterol Δ24-reductase (DHCR24), the last enzyme in the Bloch cholesterol biosynthetic pathway. The results obtained support the hypothesis of a co-evolution of the Na+,K+-ATPase and DHCR24. The evolutionary correlation between DHCR24 and the Na+,K+-ATPase was found to be stronger than between DHCR24 and any other membrane protein investigated. The results obtained, thus, also support the hypothesis that cholesterol evolved together with the Na+,K+-ATPase in multicellular animals to support Na+,K+-ATPase activity.en
dc.description.sponsorshipAustralian Research Councilen
dc.language.isoen_AUen
dc.publisherSpringeren
dc.relationARC DP121003548, ARC DP150101112en
dc.rightsOtheren
dc.subjectsodium pumpen
dc.subjectplasma membraneen
dc.subject3beta-hydroxysterol Delta24-reductaseen
dc.subjectsqualene monooxygenaseen
dc.subjectmirror tree analysisen
dc.titleStimulation of Na+,K+-ATPase activity as a possible driving foce in cholesterol evolutionen
dc.typeArticleen
dc.subject.asrcFoR::030403 - Characterisation of Biological Macromoleculesen
dc.identifier.doidoi 10.1007/s00232-015-9864-z
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcDP121003548
dc.relation.arcDP150101112
dc.rights.otherThis is a post-peer-review, pre-copyedit version of an article published in The Journal of Membrane Biology. The final authenticated version is available online at: doi 10.1007/s00232-015-9864-z.en
usyd.facultySeS faculties schools::Faculty of Scienceen


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