Genetic Effect Analysis of β-globin Gene 3'UTR+101G>C (HBB:c. *233G>C) Variant.
10.19746/j.cnki.issn.1009-2137.2021.04.040
- Author:
Li DU
1
;
Cui-Ze YAO
1
;
Xiu-Qin BAO
1
;
Jie LIANG
1
;
Teng-Long YUAN
1
;
Dan-Qing QIN
2
;
Ji-Cheng WANG
3
Author Information
1. Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangdong Birth Defect Prevention and Management Center, Guangzhou 511442, Guangdong Province, China.
2. Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangdong Birth Defect Prevention and Management Center, Guangzhou 511442, Guangdong Province, China E-mail : qindanqing1985@163.com.
3. Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangdong Birth Defect Prevention and Management Center, Guangzhou 511442, Guangdong Province, China E-mail: jicheng0927@126.com.
- Publication Type:Journal Article
- MeSH:
3' Untranslated Regions;
Hemoglobins, Abnormal/genetics*;
Humans;
Mutation;
beta-Globins/genetics*;
beta-Thalassemia/genetics*
- From:
Journal of Experimental Hematology
2021;29(4):1271-1274
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate whether β-globin gene 3'UTR+101G>C (HBB:c.*233G>C) variant has genetic effect and provide basis for gene diagnosis and genetic counseling.
METHOD:Whole blood cell analysis and capillary zone electrophoresis (CZE) were used to analyze the hematological indexes. The most frequent 23 mutations in southern Chinese individuals were routinely measured by PCR-flow fluorenscence immunmicrobeads assay. Sanger sequencing was used to detect the other variants of β-globin gene (HBB).
RESULTS:In 463 cases, a total of 7 cases with HBB:c.*233G>C variant were detected, among them 4 cases carried other pathogenic variants of HBB gene (2 cases were in trans, 2 cases were in cis), who had typical hematological characteristics of mild β-thalassemia, and 3 cases also carried abnormal hemoglobin variation, but did not have hematological characteristics of β-thalassemia.
CONCLUSION:The study shows that HBB:c.*233G > C variant has no obvious genetic effect and should be a benign polymorphism.
