Analysis of the molecular characterization of a Chinese pedigree with rare β thalassemia genotype
10.3760/cma.j.issn.1009-9158.2011.07.004
- VernacularTitle:中国人群中少见β地中海贫血家系的分子遗传学特征分析
- Author:
Ge HUANG
;
Xiaosui HUANG
;
Xianling LUO
;
Wenling JIANG
;
Yunxiong LI
;
Dong CHEN
- Publication Type:Journal Article
- Keywords:
beta-Thalassemia;
Pedigree;
Globins;
Mutation;
Two-hybrid system techniques
- From:
Chinese Journal of Laboratory Medicine
2011;34(7):591-594
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the molecular characterization of a Chinese pedigree with rare β thalassemia genotype.Methods Phenotypic analysis was performed using standard hematological tests to measure red blood cell parameters, including RBC,Hb,MCV,MCH,MCHC and RDW.SPIFE automatic Hb agarose gel electrophoresis instrument was used to measure hemoglobin fraction Hb A,Hb A2 and Hb F.The alleles of β thalassemia mutation were determined by RDB assay, and then cloning and sequencing were performed to define the mutation sites.Results The proband and his father had typical microcytic hypochromic anemia with low MCV and MCH(79.8, 63.1 fl and 19.9, 20.9 pg, respectively) and high level of Hb A2 (5.66% and 5.60%, respectively).The proband′s mother had normal MCV and MCH. β thalassemia mutation analysis with RDB assay showed that the proband had thalassemia minor resulting from double mutations on one globin gene.One showed codons 41/42 (-TTCT) mutation and the other was CAP mutation from positions +40 to +43 in the promoter region.These two mutations were inherited from his father.The genotype of the proband and his father was β41/42、CAP/βA ,and the genotype of his mother was βA/βA.Conclusions It′s rare that double mutations occur on single β globin gene, with one mutation on CD41/42(-TTCT) and the other mutation from positions +40 to +43 relative to the mRNA cap site in the promoter region.The findings enrich knowledge of the mutation spectrum of β thalassemia.
