Martins Juliana T N, Bordin Silvana, de Albuquerque Dulcinéia M, Saad Sara T O, Costa Fernando F
Haematology and Haemotherapy Centre, State University of Campinas, São Paulo, Brazil.
Hemoglobin. 2005;29(1):85-9.
Analysis of DNA polymorphic sites is an important tool for the detection of gene flow in human evolutionary studies and to study the genetic background for gene mutations. The beta-globin locus contains several single-base restriction fragment length polymorphism (RFLP) sites throughout chromosome 11. In addition to these polymorphic sequence repeats, others are being studied in order to expand our knowledge concerning the role between haplotype-genotype and phenotype associations. Far downstream of the expressed beta-globin genes, there is a hypersensitive site (HS) whose function remains obscure. We sequenced this region in 27 thalassemia patients and found a new pattern in the micro-satellite-like AT-rich region of this site: a new TAA insertion in addition to the one previously described in sickle cell patients with a concomitant polymorphism (G-->A). This new variation was found to be linked to the IVS-I-6 (T-->C) mutation. This polymorphism may be useful for studies concerning genotype and phenotype associations.
DNA多态性位点分析是人类进化研究中检测基因流以及研究基因突变遗传背景的重要工具。β-珠蛋白基因座在11号染色体上包含多个单碱基限制性片段长度多态性(RFLP)位点。除了这些多态性序列重复外,其他一些也正在被研究,以扩展我们对单倍型-基因型和表型关联之间作用的认识。在表达的β-珠蛋白基因的下游很远的地方,有一个超敏位点(HS),其功能仍然不清楚。我们对27名地中海贫血患者的该区域进行了测序,在这个位点的微卫星样富含AT的区域发现了一种新模式:除了先前在镰状细胞患者中描述的伴有多态性(G→A)的一个TAA插入外,还有一个新的TAA插入。发现这种新变异与IVS-I-6(T→C)突变相关。这种多态性可能有助于有关基因型和表型关联的研究。