The human fetal globin genes consist of the first mammalian genomic loci for which gene conversion was reported. To date, 14 gene conversions have been described in the human Gγ- and Aγ-globin genes, the vast majority of which are restricted to the coding sequences. Here, we provide evidence for three new gene conversion events in the 5′ regulatory region of the human fetal globin genes, identified during a large genetic screening effort in adult individuals with high fetal hemoglobin (Hb) levels. The sequence variations, resulting from these conversion events, are transcriptionally silent polymorphisms that do not contribute to increased fetal Hb levels. Our results suggest that the 5′ regulatory region of the human fetal globin genes is a gene conversion hotspot that prevent globin gene promoter sequence diversification, further underlining the need for two functional fetal globin genes in fetal erythropoiesis. Copyright

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doi.org/10.1080/03630260802507824, hdl.handle.net/1765/29636
Hemoglobin: international journal for hemoglobin research
Erasmus MC: University Medical Center Rotterdam

Kalamaras, A., Chassanidis, C., Samara, M., Chiotoglou, I., Vamvakopoulos, N., Papadakis, M., … Patrinos, G. (2008). The 5′ regulatory region of the human fetal globin genes is a gene conversion hotspot. Hemoglobin: international journal for hemoglobin research, 32(6), 572–581. doi:10.1080/03630260802507824