Publication:
The story of a ship journey, malaria, and the HBB gene ivs-ii-745 mutation: Circassian immigration to cyprus

dc.contributor.authorErgören, Mahmut C.
dc.contributor.authorTemel, Şehime G.
dc.contributor.authorMocan, Gamze
dc.contributor.authorDündar, Munis
dc.contributor.buuauthorTemel, Şehime G.
dc.contributor.buuauthorTEMEL, ŞEHİME GÜLSÜN
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Genetik Mühendisliği Anabilim Dalı.
dc.contributor.orcid0000-0001-9593-9325
dc.contributor.orcid0000-0002-9802-0880
dc.contributor.orcid0000-0003-0969-4611
dc.contributor.researcheridB-3150-2011
dc.contributor.researcheridD-8491-2018
dc.contributor.researcheridGQP-2509-2022
dc.contributor.researcheridAAZ-6885-2021
dc.date.accessioned2024-06-05T11:58:19Z
dc.date.available2024-06-05T11:58:19Z
dc.date.issued2021-03-16
dc.description.abstractBackground During 19th century, the Circassians were secluded from their lands and forced to migrate to Ottoman Empire properties. Approximately 2,346 Circassians were exiled from Istanbul to Cyprus Island. During the deportation journey, many of Circassian were passed away in consequence of malaria and unknown reasons. Overall, 1,351 survivor Circassians managed to reach the island, however, many of them had faced with endemic malaria again in Cyprus. An autosomal recessive hematological disorder thalassemia was the second endemic health condition after malaria, whereas thalassemia carriers show resistance to malaria infections.Materials and Methods A large Cypriot family with 57 members whose grandparents were supposed to be in that ship journey has been investigated in this study. Polymerase chain reaction (PCR)-amplification refractory mutation system (ARMS) analysis technique was used for genotyping the HHB gene.Results The human beta -globin ( HBB ) gene c.316-106C>G (IVS-II-745) (II-745) heterozygous variation have been detected.Conclusion Overall, this study is a very good example for a typical natural selection. In this case, one single gene point mutation did not limit survival in the society; natively, it increased their survival changes to form new colonization and the inheritance of the mutation to the next generations.
dc.identifier.doi10.1055/s-0041-1726336
dc.identifier.endpage71
dc.identifier.issn2699-9404
dc.identifier.issue2
dc.identifier.startpage69
dc.identifier.urihttps://doi.org/10.1055/s-0041-1726336
dc.identifier.urihttps://hdl.handle.net/11452/41776
dc.identifier.volume8
dc.identifier.wos000629809100003
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherThieme Medical Publication
dc.relation.journalGlobal Medical Genetics
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBeta-thalassemia mutations
dc.subjectPopulation
dc.subjectCircassians
dc.subject&#946
dc.subject-thalassemia
dc.subjectIvs-ii-745
dc.subjectCyprus
dc.subjectMalaria
dc.subjectGenetic fitness
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectGenetics & heredity
dc.subjectGenetics & heredity
dc.titleThe story of a ship journey, malaria, and the HBB gene ivs-ii-745 mutation: Circassian immigration to cyprus
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationf513efaa-a54e-4cfa-840f-28e2fbdc001a
relation.isAuthorOfPublication.latestForDiscoveryf513efaa-a54e-4cfa-840f-28e2fbdc001a

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