Abstract
BackgroundThalassemia is one of the most common monogenic hemolytic disorders in the world. Hong Kongαα (HKαα) thalassemia was initially found among the people of southern China. Because of the complexity of genetic changes in HKαα thalassemia, we lack a precise sequence analysis of the HKαα allele. Here we aim to detect the specific genotype and trace the law of inheritance of this rare genotype.MethodsWe recruited an unprecedented huge pedigree containing 11 individuals carrying the HKαα thalassemia gene and 4 nongenetic‐related patients suffering from HKαα from south China. Regular hematological analysis and routine genetic screening were performed on the pedigree and two‐round nested PCR (polymerase chain reaction) for HKαα thalassemia were performed on each individual. The first‐generation gene sequencing was performed on six individuals, including four nongenetic‐related patients.ResultWe found that five family members were positive for the HKαα allele. Patients Ⅱ‐2, Ⅲ‐1, and Ⅱ‐3 with only HKαα/‐‐SEA or HKαα/‐α4.2 presented with α‐thalassemia minor trait. Ⅰ‐1, the carrier of both HKαα/‐α3.7 and β41‐42/βN, showed a typical β‐thalassemia trait. Fetus with genotype HKαα/‐α4.2 alone was not likely to suffer from any deleterious effects after birth. The whole sequence of HKαα allele revealed that HKαα alleles in the six patients shared a high similarity, implying that all HKαα alleles are likely from the same ancestor. Moreover, pedigree and sequencing analyses demonstrated that the HKαα allele contained αααanti4.2 mutation, ‐α3.7 mutation, and a fragment from α‐hemoglobin gene; thus, the composition and formation of HKαα allele was revealed. Finally, the high similarity and composition of HKαα alleles implies that once HKαα formed, αααanti4.2 and ‐α3.7 mutations tended to be a fusion gene and quite impossible to be inherited separately.ConclusionThe two‐round nested PCR is an effective method to detect HKαα allele. Besides, our study for the first time revealed the sequence of the HKαα allele, the evidence of the same ancestor with HKαα thalassemia and enriched the composition as well as the formation mechanism of HKαα allele, and immediately opened up novel potential diagnosis and prenatal counseling for HKαα thalassemia.
Highlights
Thalassemia, the most common monogenic disorder in the world (Weatherall & Clegg, 1996), is caused by genetic defects affecting hemoglobin gene expression
The two-round nested polymerase chain reaction (PCR) is an effective method for Hong Kongαα (HKαα) thalassemia diagnosis (Wang et al, 2005), it is too complicated and uneconomical to perform in clinical laboratories
We found the presence of an anomalous fragment in II-2 and II-3, who were positive for --SEA and -α3.7 alleles, as well as in III-1 and III-2 who were positive for -α3.7 and -α4.2 alleles (Figure 1)
Summary
Thalassemia, the most common monogenic disorder in the world (Weatherall & Clegg, 1996), is caused by genetic defects affecting hemoglobin gene expression. Deletional mutations account for the majority of the α-thalassemia cases, of which the SEA deletion (--SEA), the rightward deletion (-α3.7), and the leftward deletion (-α4.2) contribute to up to 61.37%, 18.52%, and 6.80%, respectively, of the disease cases in Guilin, Guangxi, China (Tang et al, 2015). HKαα thalassemia is not as common as other deletional types of α-thalassemia or point mutation types of β-thalassemia, with a carrier rate of 0.07% (Shang et al, 2013) in the population of Guangxi, China. The two-round nested PCR is an effective method for HKαα thalassemia diagnosis (Wang et al, 2005), it is too complicated and uneconomical to perform in clinical laboratories. We successfully identified the sequence of HKαα thalassemia and provide a novel potential diagnosis and prenatal counseling strategy for the disease
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