Kalamaras Angelos, Chassanidis Christos, Samara Maria, Chiotoglou Ioanna, Vamvakopoulos Nikolaos K, Papadakis Manoussos N, Kollia Panagoula, Patrinos George P
Department of Biology, School of Medicine, University of Thessaly, Larissa, Greece.
Hemoglobin. 2008;32(6):572-81. doi: 10.1080/03630260802507824.
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 Ggamma- and Agamma-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.
人类胎儿珠蛋白基因是首个被报道发生基因转换的哺乳动物基因组位点。迄今为止,已在人类γ-珠蛋白基因和δ-珠蛋白基因中描述了14次基因转换,其中绝大多数仅限于编码序列。在这里,我们提供了人类胎儿珠蛋白基因5'调控区域中三个新的基因转换事件的证据,这些事件是在对成年个体进行的大规模基因筛查中发现的,这些个体具有高胎儿血红蛋白(Hb)水平。这些转换事件导致的序列变异是转录沉默多态性,不会导致胎儿Hb水平升高。我们的结果表明,人类胎儿珠蛋白基因的5'调控区域是一个基因转换热点,可防止珠蛋白基因启动子序列多样化,进一步强调了在胎儿红细胞生成中需要两个功能性胎儿珠蛋白基因。