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Published in: Indian Journal of Hematology and Blood Transfusion 1/2016

01-06-2016 | Correspondence

The Frequency of α-Globin Gene Triplication in a Southern Chinese Population

Authors: Man-Yu Wu, Jian-Ying Zhou, Jian Li, Dong-Zhi Li

Published in: Indian Journal of Hematology and Blood Transfusion | Special Issue 1/2016

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Excerpt

Alpha gene number plays an important role in modulating the phenotype of thalassemia. It has been known that the coexistence of α-globin gene triplication (ααα) is an important modulator of the severity of β-thalassemia trait, exacerbating the phenotypic severity of β-thalassemia by causing more globin chain imbalance [1, 2]. Therefore characterization of α-globin gene mutations can be of great help in identification of hemoglobinopathies. Different frequencies of α-globin triplication have already been reported in many populations [36]. However, there has been no epidemiological study of α-globin gene triplication in Chinese. Here, we report the prevalence of α-globin triplication in a southern China population with high prevalence of β-thalassemia. …
Literature
4.
go back to reference Peres MJ, Romao L, Carreiro H et al (1995) Molecular basis of α-thalassemia in Portugal. Hemoglobin 19:343–352CrossRefPubMed Peres MJ, Romao L, Carreiro H et al (1995) Molecular basis of α-thalassemia in Portugal. Hemoglobin 19:343–352CrossRefPubMed
5.
go back to reference Giordano PC, Bakker-Verwij M, Harteveld CL (2009) Frequency of α-globin gene triplications and their interaction with β-thalassemia mutations. Hemoglobin 33:124–131CrossRefPubMed Giordano PC, Bakker-Verwij M, Harteveld CL (2009) Frequency of α-globin gene triplications and their interaction with β-thalassemia mutations. Hemoglobin 33:124–131CrossRefPubMed
6.
go back to reference Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K (2008) Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test 12:177–180CrossRefPubMed Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K (2008) Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test 12:177–180CrossRefPubMed
7.
go back to reference Wang W, Ma ES, Chan AY et al (2003) Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications. Clin Chem 49:1679–1682CrossRefPubMed Wang W, Ma ES, Chan AY et al (2003) Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications. Clin Chem 49:1679–1682CrossRefPubMed
8.
go back to reference Wang W, Chan AY, Chan LC et al (2005) Unusual rearrangement of the α-globin gene cluster containing both the -α3.7 and αααanti4.2 crossover junctions: clinical diagnostic implications and possible mechanisms. Clin Chem 51:2167–2170CrossRefPubMed Wang W, Chan AY, Chan LC et al (2005) Unusual rearrangement of the α-globin gene cluster containing both the -α3.7 and αααanti4.2 crossover junctions: clinical diagnostic implications and possible mechanisms. Clin Chem 51:2167–2170CrossRefPubMed
9.
go back to reference Shang X, Li Q, Cai R, Huang J, Wei X, Xu X (2013) Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects. Clin Genet 83:472–476CrossRefPubMed Shang X, Li Q, Cai R, Huang J, Wei X, Xu X (2013) Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects. Clin Genet 83:472–476CrossRefPubMed
10.
go back to reference Chen W, Zhang X, Shang X et al (2010) The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity. BMC Med Genet 11:31CrossRefPubMedPubMedCentral Chen W, Zhang X, Shang X et al (2010) The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity. BMC Med Genet 11:31CrossRefPubMedPubMedCentral
11.
go back to reference Wu MY, Li J, Li SC, Li R, Liao C, Li DZ (2015) Compound heterozygosity for HKαα and an in cis deletion of double α genes presents as α-thalassemia trait. Hemoglobin 39:256–259CrossRefPubMed Wu MY, Li J, Li SC, Li R, Liao C, Li DZ (2015) Compound heterozygosity for HKαα and an in cis deletion of double α genes presents as α-thalassemia trait. Hemoglobin 39:256–259CrossRefPubMed
Metadata
Title
The Frequency of α-Globin Gene Triplication in a Southern Chinese Population
Authors
Man-Yu Wu
Jian-Ying Zhou
Jian Li
Dong-Zhi Li
Publication date
01-06-2016
Publisher
Springer India
Published in
Indian Journal of Hematology and Blood Transfusion / Issue Special Issue 1/2016
Print ISSN: 0971-4502
Electronic ISSN: 0974-0449
DOI
https://doi.org/10.1007/s12288-015-0588-0

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