Khatami Shohreh, Najmabadi Hossein, Rouhi Soghra, Mirzazadeh Roghieh, Bayat Parastoo, Sadeghi Sedigheh
Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.
Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.
Arch Iran Med. 2013 Dec;16(12):739-40.
Many abnormal α-chain hemoglobins (Hbs) are caused by single nucleotide mutations in α1- or α2-goblin genes. One of these Hbs is Hb Q-Iran which is resulted from a point mutation at codon 75 of the α1-globin gene (Asp→His). The identification of Hb Q-Iran was observed in two members of a family from the Central Province of Iran. In this study, Globin chain analysis on high performance liquid chromatography (HPLC) and DNA sequencing were applied. An unusual Hb variant, like HbS on alkaline pH electrophoresis was identified from samples of a father and his son from Arak city in the Central Province of Iran. The variant was further characterized by globin chain analysis and DNA sequencing methods. Globin chain analysis revealed an unknown globin chain peak after α-globin chain peak with a different retention time from βs-globin chain, as the control in both samples. Genetic analysis led to the identification of an unknown Hb variant, Hb Q-Iran. Globin chain analysis showed the presence of an unknown globin chain, and likewise DNA sequencing revealed HbQ-Iran. In other words, Globin chain analysis procedure could preliminarily detect an unknown globin chain.
许多异常α链血红蛋白(Hb)是由α1或α2珠蛋白基因中的单核苷酸突变引起的。其中一种Hb是Hb Q-Iran,它是由α1珠蛋白基因第75密码子的点突变(天冬氨酸→组氨酸)导致的。在伊朗中部省份的一个家族的两名成员中发现了Hb Q-Iran。在本研究中,应用了高效液相色谱(HPLC)上的珠蛋白链分析和DNA测序。从伊朗中部省份阿拉克市的一名父亲及其儿子的样本中,在碱性pH电泳上鉴定出一种异常的Hb变体,类似于HbS。通过珠蛋白链分析和DNA测序方法对该变体进行了进一步表征。珠蛋白链分析显示,在两个样本作为对照的情况下,α珠蛋白链峰之后有一个未知的珠蛋白链峰,其保留时间与βs珠蛋白链不同。基因分析导致鉴定出一种未知的Hb变体,即Hb Q-Iran。珠蛋白链分析显示存在一条未知的珠蛋白链,同样,DNA测序揭示了HbQ-Iran。换句话说,珠蛋白链分析程序可以初步检测到一条未知的珠蛋白链。