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dc.creatorVavougios G.D.en
dc.date.accessioned2023-01-31T10:30:06Z
dc.date.available2023-01-31T10:30:06Z
dc.date.issued2020
dc.identifier10.1016/j.mehy.2020.110212
dc.identifier.issn03069877
dc.identifier.urihttp://hdl.handle.net/11615/80522
dc.description.abstractSARS-CoV-2 neurotropism has been increasingly recognized by its imaging and syndromic manifestations in the literature. The purpose of this report is to explore the limited yet salient current evidence that SARS-CoV-2′s host genomic targets PTBP1 and the 14-3-3 protein isoform encoding genes YWHAE and YWHAZ may be hold the key to understanding how neurotropism triggers neurodegeneration and how it may contribute to the onset of neurodegenerative disease. Considering that PTBP1 silencing in particular has recently been shown to reverse clinical parkinsonism and induce neurogenesis, as well as the known interactions of PTBP1 and YWHAE/Z with coronaviruses – most notably 14-3-3 and SARS-CoV, recent studies reinvigorate the infectious etiology hypotheses on major neurodegenerative disease such as AD and iPD. Considering that human coronaviruses with definite neurotropism have been shown to achieve long-term latency within the mammalian CNS as a result of specific accommodating mutations, the corroboration of genomic-level evidence with neuroimaging has vast potential implications for neurodegenerative disease. © 2020 Elsevier Ltden
dc.language.isoenen
dc.sourceMedical Hypothesesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85090020357&doi=10.1016%2fj.mehy.2020.110212&partnerID=40&md5=0350988bb803870801d0e1a6ba3d71d9
dc.subjectpolypyrimidine tract binding proteinen
dc.subjectprotein 14 3 3en
dc.subjectPTBP1 proteinen
dc.subjectunclassified drugen
dc.subjectYWHAE proteinen
dc.subjectYWHAZ proteinen
dc.subjectheterogeneous nuclear ribonucleoproteinen
dc.subjectpolypyrimidine tract binding proteinen
dc.subjectprotein 14 3 3en
dc.subjectPTBP1 protein, humanen
dc.subjectYWHAE protein, humanen
dc.subjectYWHAZ protein, humanen
dc.subjectAlzheimer diseaseen
dc.subjectArticleen
dc.subjectgene expressionen
dc.subjectgene silencingen
dc.subjectnerve degenerationen
dc.subjectnervous system developmenten
dc.subjectneuroimagingen
dc.subjectneurotropismen
dc.subjectnonhumanen
dc.subjectParkinson diseaseen
dc.subjectparkinsonismen
dc.subjectprotein protein interactionen
dc.subjectprotein targetingen
dc.subjectSevere acute respiratory syndrome coronavirus 2en
dc.subjectvirus cell interactionen
dc.subjectvirus latencyen
dc.subjectvirus mutationen
dc.subjectbiological modelen
dc.subjectcomplicationen
dc.subjectdegenerative diseaseen
dc.subjectgene expression regulationen
dc.subjectgeneticsen
dc.subjecthumanen
dc.subjectnerve degenerationen
dc.subjectpandemicen
dc.subjectpathogenicityen
dc.subjectvirologyen
dc.subject14-3-3 Proteinsen
dc.subjectCOVID-19en
dc.subjectGene Expression Regulationen
dc.subjectHeterogeneous-Nuclear Ribonucleoproteinsen
dc.subjectHost Microbial Interactionsen
dc.subjectHumansen
dc.subjectModels, Neurologicalen
dc.subjectNerve Degenerationen
dc.subjectNeurodegenerative Diseasesen
dc.subjectPandemicsen
dc.subjectPolypyrimidine Tract-Binding Proteinen
dc.subjectSARS-CoV-2en
dc.subjectChurchill Livingstoneen
dc.titleSARS-CoV-2 dysregulation of PTBP1 and YWHAE/Z gene expression: A primer of neurodegenerationen
dc.typejournalArticleen


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