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dc.contributor.authorLove, Nick R.eng
dc.contributor.authorZiegler, Mathiaseng
dc.contributor.authorChen, Yaoyaoeng
dc.contributor.authorAmaya, Enriqueeng
dc.date.accessioned2015-03-09T11:54:02Z
dc.date.available2015-03-09T11:54:02Z
dc.date.issued2014-01eng
dc.identifier.issn0265-9247en_US
dc.identifier.urihttps://hdl.handle.net/1956/9488
dc.description.abstractWe recently examined gene expression during Xenopus tadpole tail appendage regeneration and found that carbohydrate regulatory genes were dramatically altered during the regeneration process. In this essay, we speculate that these changes in gene expression play an essential role during regeneration by stimulating the anabolic pathways required for the reconstruction of a new appendage. We hypothesize that during regeneration, cells use leptin, slc2a3, proinsulin, g6pd, hif1α expression, receptor tyrosine kinase (RTK) signaling, and the production of reactive oxygen species (ROS) to promote glucose entry into glycolysis and the pentose phosphate pathway (PPP), thus stimulating macromolecular biosynthesis. We suggest that this metabolic shift is integral to the appendage regeneration program and that the Xenopus model is a powerful experimental system to further explore this phenomenon.en_US
dc.language.isoengeng
dc.publisherWileyen_US
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/eng
dc.subjectgenetically encoded indicatoreng
dc.subjectglycolysiseng
dc.subjectMetabolismeng
dc.subjectpentose phosphate pathwayeng
dc.subjecttissue regenerationeng
dc.subjectWarburg effecteng
dc.subjectXenopus tadpole tail regenerationeng
dc.titleCarbohydrate metabolism during vertebrate appendage regeneration: What is its role? How is it regulated? A postulation that regenerating vertebrate appendages facilitate glycolytic and pentose phosphate pathways to fuel macromolecule biosynthesisen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2015-03-06T07:15:52Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2013 The Authorsen_US
dc.identifier.doihttps://doi.org/10.1002/bies.201300110
dc.identifier.cristin1126737
dc.source.journalBioessays
dc.source.4036
dc.source.141
dc.source.pagenumber27-33


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Attribution CC BY
Except where otherwise noted, this item's license is described as Attribution CC BY