Genetic recombination as a major cause of mutagenesis in the human globin gene clusters

被引:25
作者
Borg, Joseph [2 ,3 ]
Georgitsi, Marianthi [1 ]
Aleporou-Marinou, Vassiliki [4 ]
Kollia, Panagoula [4 ]
Patrinos, George P. [1 ,2 ]
机构
[1] Univ Patras, Sch Hlth Sci, Dept Pharm, GR-26504 Patras, Greece
[2] Erasmus MC, Fac Med & Hlth Sci, MGC, Dept Cell Biol & Genet, Rotterdam, Netherlands
[3] Univ Malta, Sch Med, Mol Genet Lab, Msida, Malta
[4] Univ Athens, Dept Biol, Sch Phys Sci, GR-15701 Athens, Greece
关键词
Genetic recombination; Unequal crossover; Gene conversion; Globin genes; Mutation; Thalassemia; Sickle cell disease; NONDELETIONAL HEREDITARY PERSISTENCE; G-GAMMA-GLOBIN; HUMAN HEMOGLOBIN-VARIANTS; BETA-DEGREES-THALASSEMIA; SICKLE-CELL MUTATION; LOCUS-CONTROL REGION; HB F-CHARLOTTE; HUMAN A-GAMMA; FETAL GLOBIN; NUCLEOTIDE-SEQUENCES;
D O I
10.1016/j.clinbiochem.2009.07.014
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Homologous recombination is a frequent phenomenon in multigene families and as such it occurs several times in both the alpha- and beta-like globin gene families. In numerous occasions, genetic recombination has been previously implicated as a major mechanism that drives mutagenesis in the human globin gene clusters, either in the form of unequal crossover or gene conversion. Unequal crossover results in the increase or decrease of the human globin gene copies, accompanied in the majority of cases with minor phenotypic consequences, while gene conversion contributes either to maintaining sequence homogeneity or generating sequence diversity. The role of genetic recombination, particularly gene conversion in the evolution of the human globin gene families has been discussed elsewhere. Conclusion: Here, we summarize our current knowledge and review existing experimental evidence outlining the role of genetic recombination in the mutagenic process in the human globin gene families. (C) 2009 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1839 / 1850
页数:12
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