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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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SARS-CoV-2 dysregulation of PTBP1 and YWHAE/Z gene expression: A primer of neurodegeneration

Thumbnail
Autor
Vavougios G.D.
Datum
2020
Language
en
DOI
10.1016/j.mehy.2020.110212
Schlagwort
polypyrimidine tract binding protein
protein 14 3 3
PTBP1 protein
unclassified drug
YWHAE protein
YWHAZ protein
heterogeneous nuclear ribonucleoprotein
polypyrimidine tract binding protein
protein 14 3 3
PTBP1 protein, human
YWHAE protein, human
YWHAZ protein, human
Alzheimer disease
Article
gene expression
gene silencing
nerve degeneration
nervous system development
neuroimaging
neurotropism
nonhuman
Parkinson disease
parkinsonism
protein protein interaction
protein targeting
Severe acute respiratory syndrome coronavirus 2
virus cell interaction
virus latency
virus mutation
biological model
complication
degenerative disease
gene expression regulation
genetics
human
nerve degeneration
pandemic
pathogenicity
virology
14-3-3 Proteins
COVID-19
Gene Expression Regulation
Heterogeneous-Nuclear Ribonucleoproteins
Host Microbial Interactions
Humans
Models, Neurological
Nerve Degeneration
Neurodegenerative Diseases
Pandemics
Polypyrimidine Tract-Binding Protein
SARS-CoV-2
Churchill Livingstone
Zur Langanzeige
Zusammenfassung
SARS-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 Ltd
URI
http://hdl.handle.net/11615/80522
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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