The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus

C. Ergoren Mahmut, G. Temel Sehime, Mocan Gamze, Dundar Munis

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Global Medical Genetics ›› 2021, Vol. 8 ›› Issue (02) : 69-71. DOI: 10.1055/s-0041-1726336
Orginal Article
Orginal Article

The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus

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Abstract

Background 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 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 β-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.

Keywords

Circassians / β-thalassemia / IVS-II-745 / Cyprus / malaria / genetic fitness

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C. Ergoren Mahmut, G. Temel Sehime, Mocan Gamze, Dundar Munis. The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus. Global Medical Genetics, 2021, 8(02): 69‒71 https://doi.org/10.1055/s-0041-1726336

References

[1]
Abreg A.Geçmişten Günümüze Kafkasların Trajedisi. Istanbul: Kafkas Vakfi Yayinlari; 2006:43
[2]
Allen WED, Muratoff P. 1828-1921 Türk-Kafkas Sınırındaki Harplerin Tarihi. Genelkurmay Başkanlığı Yayınları Ankara, Turkey: Genelkurmay Başkanlığı; 1966:104
[3]
Sasmaz M.Immigration and Settlemen of Circassian in the Ottoman Empire on British Documents 1857-1864. Osmanlı Tarihi Araştırma ve Uygulama Merkezi Dergisi 1999;09:331-336
[4]
World Health Organization (WHO); Community control of hereditary anemias, memorandum from a WHO meeting. Bull World Health Organ 1983;61(01):63-80
[5]
Modell B, Berdoukas V.Thalassaemia in Cyprus. In: Modell B, Berdoukas V, eds. The Clinical Approaches to Thalassaemia. London, United Kingdom: Grune & Stratton; 1984:263-277
[6]
Bozkurt G.Results from the north cyprus thalassemia prevention program. Hemoglobin 2007;31(02):257-264
[7]
Kent G.Total victory over malaria. Read Dig 1951:77-79
[8]
Haldane JBS.The rate of mutations of human genes. Hered Suppl 1949;35:267-273
[9]
Aziz M.History of prevention of malaria in Cyprus. Cyprus Med J 1947;1(02):13-17
[10]
Sozuöz A, Berkalp A, Figus A, Loi A, Pirastu M, Cao A.β thalassaemia mutations in Turkish Cypriots. J Med Genet 1988;25(11): 766-768
[11]
Baysal E, Indrak K, Bozkurt G, et al.The β-thalassaemia mutations in the population of Cyprus. Br J Haematol 1992;81(04): 607-609
[12]
Kountouris P, Kousiappa I, Papasavva T, et al.The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study. Sci Rep 2016;6:26371
[13]
Grmek MD.-Malaria in the eastern Mediterranean in prehistory and antiquity-. Parassitologia 1994;36(1,2):1-6
[14]
Orkin SH, Kazazian HH Jr., Antonarakis SE, et al.Linkage of betathalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster. Nature 1982;296(5858):627-631
[15]
Tadmouri GO, Başak AN.β-thalassemia in Turkey: a review of the clinical, epidemiological, molecular, and evolutionary aspects. Hemoglobin 2001;25(02):227-239
[16]
Tadmouri GO, Tüzmen S, Ozçelik H, et al.Molecular and population genetic analyses of beta-thalassemia in Turkey. AmJ Hematol 1998;57(03):215-220

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