Bioinformatics analysis of allele frequencies and expression patterns of ace2, tmprss2 and furin in different populations and susceptibility to sars-cov-2

dc.contributor.authorTarek, Mohammad M.
dc.contributor.authorAbdelzaher, Hana M.
dc.contributor.authorKobeissy, Firas H.
dc.contributor.authorEl-Fawal, Hassan A.N.
dc.contributor.authorSalama, Mohamed M.
dc.contributor.authorAbdelnaser, Anwar
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:38:16Z
dc.date.available2025-01-24T11:38:16Z
dc.date.issued2021
dc.description.abstractThe virus responsible for the COVID-19 global health crisis, SARS-CoV-2, has been shown to utilize the ACE2 protein as an entry point to its target cells. The virus has been shown to rely on the actions of TMPRSS2 (a serine protease), as well as FURIN (a peptidase), for the critical priming of its spike protein. It has been postulated that variations in the sequence and expression of SARS-CoV-2’s receptor (ACE2) and the two priming proteases (TMPRSS2 and FURIN) may be critical in contributing to SARS-CoV-2 infectivity. This study aims to examine the different expression levels of FURIN in various tissues and age ranges in light of ACE2 and TMPRSS2 expression levels using the LungMAP database. Furthermore, we retrieved expression quantitative trait loci (eQTLs) of the three genes and their annotation. We analyzed the frequency of the retrieved variants in data from various populations and compared it to the Egyptian population. We highlight FURIN’s potential interplay with the immune response to SARS-CoV-2 and showcase a myriad of variants of the three genes that are differentially expressed across populations. Our findings provide insights into potential genetic factors that impact SARS-CoV-2 infectivity in different populations and shed light on the varying expression patterns of FURIN. © 2021 by the author. Licensee MDPI, Basel, Switzerland.
dc.identifier.doihttps://doi.org/10.3390/genes12071041
dc.identifier.eid2-s2.0-85110342283
dc.identifier.pmid34356057
dc.identifier.urihttp://hdl.handle.net/10938/29026
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofGenes
dc.sourceScopus
dc.subjectAce2
dc.subjectCovid-19
dc.subjectEqtls
dc.subjectFurin
dc.subjectSars-cov-2
dc.subjectTmprss2
dc.subjectVariants
dc.subjectAlleles
dc.subjectAngiotensin-converting enzyme 2
dc.subjectComputational biology
dc.subjectDatabases, nucleic acid
dc.subjectFemale
dc.subjectGene expression regulation, enzymologic
dc.subjectGene frequency
dc.subjectGenetic predisposition to disease
dc.subjectHumans
dc.subjectMale
dc.subjectSerine endopeptidases
dc.subjectAngiotensin converting enzyme 2
dc.subjectTransmembrane protease serine 2
dc.subjectAce2 protein, human
dc.subjectFurin protein, human
dc.subjectSerine proteinase
dc.subjectTmprss2 protein, human
dc.subjectArticle
dc.subjectBioinformatics
dc.subjectCase fatality rate
dc.subjectControlled study
dc.subjectCoronavirus disease 2019
dc.subjectExpression quantitative trait locus
dc.subjectGene expression
dc.subjectGene expression level
dc.subjectGene mutation
dc.subjectGenetic association
dc.subjectGenetic susceptibility
dc.subjectGenetic variability
dc.subjectHuman
dc.subjectHuman tissue
dc.subjectImmune response
dc.subjectMortality
dc.subjectProtein expression
dc.subjectRna sequencing
dc.subjectSevere acute respiratory syndrome coronavirus 2
dc.subjectSingle nucleotide polymorphism
dc.subjectVirus infectivity
dc.subjectVirus transmission
dc.subjectAllele
dc.subjectBiology
dc.subjectBiosynthesis
dc.subjectEnzymology
dc.subjectGene expression regulation
dc.subjectGenetic predisposition
dc.subjectGenetics
dc.subjectMetabolism
dc.subjectNucleic acid database
dc.titleBioinformatics analysis of allele frequencies and expression patterns of ace2, tmprss2 and furin in different populations and susceptibility to sars-cov-2
dc.typeArticle

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