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The 5′ regulatory region of the human fetal globin genes is a gene conversion hotspot

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Auteur
Kalamaras, A.; Chassanidis, C.; Samara, M.; Chiotoglou, I.; Vamvakopoulos, N. K.; Papadakis, M. N.; Kollia, P.; Patrinos, G. P.
Date
2008
DOI
10.1080/03630260802507824
Sujet
Aγ-Globin gene
Gγ-Globin gene
Fetal globin genes
Fetal hemoglobin (Hb)
Gene conversion
Sequence homogenization
Sequence variations
gamma globin
hemoglobin F
adult
article
controlled study
gene sequence
genetic polymorphism
genetic screening
genetic transcription
genotype
globin gene
hemoglobin blood level
human
nucleotide sequence
gene expression regulation
genetics
Greece
molecular genetics
mutation
regulatory sequence
Mammalia
Base Sequence
Fetal Hemoglobin
Gene Expression Regulation, Developmental
Humans
Molecular Sequence Data
Regulatory Sequences, Nucleic Acid
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Résumé
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 © Informa Healthcare USA, Inc.
URI
http://hdl.handle.net/11615/28751
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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