Clinical Laboratory, Huadu District Maternal and Neonatal Healthcare Hospital of Guangzhou, Hu Zhong Hospital, Guangzhou, People's Republic of China.
Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, People's Republic of China.
Hemoglobin. 2020 Nov;44(6):427-431. doi: 10.1080/03630269.2020.1838923. Epub 2020 Nov 4.
Genetic recombination between homologous sequences on the human globin gene clusters can lead to the creation of fusion genes. In this study, we report the detection of an α-globin fusion gene by using real-time polymerase chain reaction (qPCR)-based multicolor melting curve analysis (MMCA). The carriers of this fusion gene had a mild α-thalassemia phenotype with a normal hemoglobin (Hb) value and borderline hematological indices. Sequence analysis revealed that the mutant gene was the result of a fusion between the α2 and ψα1 genes. Our results indicate that the MMCA has the ability to detect the fusion gene, which is helpful for genetic counseling in thalassemia prevalent areas.
人类球蛋白基因簇上同源序列之间的遗传重组可能导致融合基因的产生。在这项研究中,我们报告了一种使用实时聚合酶链反应(qPCR)-多色熔解曲线分析(MMCA)检测α-球蛋白融合基因的方法。该融合基因携带者表现出轻度的α-地中海贫血表型,血红蛋白(Hb)值正常,血液学指标处于边界值。序列分析表明,突变基因是由α2 和 ψα1 基因融合产生的。我们的结果表明,MMCA 具有检测融合基因的能力,这有助于地中海贫血流行地区的遗传咨询。