Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations

被引:225
作者
Minucci, Angelo [1 ]
Moradkhani, Kamran [2 ]
Hwang, Ming Jing [3 ]
Zuppi, Cecilia [1 ]
Giardina, Bruno [1 ]
Capoluongo, Ettore [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Lab Clin Mol Diagnost, Inst Biochem & Clin Biochem, Rome, Italy
[2] AP HP, Grp Henri Mondor Albert Chenevier, Serv Biochim Genet, Creteil, France
[3] Acad Sinica, Inst Biomed Sci, Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
关键词
G6PD mutations; LOVD; Favism; RBC enzyme deficiency; DEHYDROGENASE-DEFICIENT VARIANTS; NONSPHEROCYTIC HEMOLYTIC-ANEMIA; HEMATOLOGICALLY IMPORTANT MUTATIONS; SINGLE-STRAND CONFORMATION; DIVERSE POINT MUTATIONS; MOLECULAR CHARACTERIZATION; INCREASED SUSCEPTIBILITY; GRANULOCYTE DYSFUNCTION; GENETIC-HETEROGENEITY; BASE SUBSTITUTIONS;
D O I
10.1016/j.bcmd.2012.01.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the present paper we have updated the G6PD mutations database, including all the last discovered G6PD genetic variants. We underline that the last database has been published by Vulliamy et al. [1] who analytically reported 140 G6PD mutations: along with Vulliamy's database, there are two main sites, such as http://202.120.189.88/mutdb/ and www.LOVD.nl/MR, where almost all G6PD mutations can be found. Compared to the previous mutation reports, in our paper we have included for each mutation some additional information, such as: the secondary structure and the enzyme 3D position involving by mutation, the creation or abolition of a restriction site (with the enzyme involved) and the conservation score associated with each amino acid position. The mutations reported in the present tab have been divided according to the gene's region involved (coding and non-coding) and mutations affecting the coding region in: single, multiple (at least with two bases involved) and deletion. We underline that for the listed mutations, reported in italic, literature doesn't provide all the biochemical or bio-molecular information or the research data. Finally, for the "old" mutations, we tried to verify features previously reported and, when subsequently modified, we updated the specific information using the latest literature data. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:154 / 165
页数:12
相关论文
共 131 条
[1]   G6PD KALYAN AND G6PD KERALA - 2 DEFICIENT VARIANTS IN INDIA CAUSED BY THE SAME 317 GLU-]LYS MUTATION [J].
AHLUWALIA, A ;
CORCORAN, CM ;
VULLIAMY, TJ ;
ISHWAD, CS ;
NAIDU, JM ;
ARGUSTI, A ;
STEVENS, DJ ;
MASON, PJ ;
LUZZATTO, L .
HUMAN MOLECULAR GENETICS, 1992, 1 (03) :209-210
[2]  
Ainoon Othman, 2004, Malays J Pathol, V26, P89
[3]   Molecular characterization of G6PD deficiency in southern Italy: Heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis) [J].
Alfinito, F ;
Cimmino, A ;
Ferraro, F ;
Cubellis, MV ;
Francese, M ;
Zagari, A ;
Rotoli, B ;
Filosa, S ;
Martini, G .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 98 (01) :41-46
[4]   Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD Split [J].
Barisic, M ;
Korac, J ;
Pavlinac, I ;
Krzelj, V ;
Marusic, E ;
Vulliamy, T ;
Terzic, J .
JOURNAL OF HUMAN GENETICS, 2005, 50 (11) :547-549
[5]   G6PD CAMPINAS - A DEFICIENT ENZYME WITH A MUTATION AT THE FAR 3' END OF THE GENE [J].
BARONCIANI, L ;
TRICTA, F ;
BEUTLER, E .
HUMAN MUTATION, 1993, 2 (01) :77-78
[6]   Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia [J].
Ben Daoud, B. ;
Mosbehi, I. ;
Prehu, C. ;
Chaouachi, D. ;
Hafsia, R. ;
Abbes, S. .
PATHOLOGIE BIOLOGIE, 2008, 56 (05) :260-267
[7]  
BEUTLER E, 1991, ACTA HAEMATOL-BASEL, V86, P179
[8]  
BEUTLER E, 1991, HUM GENET, V87, P462
[9]   3 NEW EXON-10 GLUCOSE-6-PHOSPHATE-DEHYDROGENASE MUTATIONS [J].
BEUTLER, E ;
WESTWOOD, B ;
MELEMED, A ;
DALBORGO, P ;
MARGOLIS, D .
BLOOD CELLS MOLECULES AND DISEASES, 1995, 21 (01) :64-72
[10]  
BEUTLER E, 1992, BLOOD, V80, P255