Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach

被引:15
作者
Douabin-Gicquel, V
Soriano, N
Ferran, H
Wojcik, F
Palierne, E
Tamim, S
Jovelin, T
McKie, AT
Le Gall, JY
David, V
Mosser, J
机构
[1] Fac Med, Dept Biochim & Biol Mol, F-35043 Rennes, France
[2] Fac Med, UMR6061, CNRS, F-35043 Rennes, France
[3] Kings Coll London, Guys Kings & St Thomas Sch Med, Dept Mol Med, London SE5, England
关键词
D O I
10.1007/s004390100599
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Single nucleotide polymorphisms (SNPs) can significantly contribute to the characterization of the genes predisposing to iron overloads or deficiencies. We report an SNP survey of coding and non-coding regions of eight genes involved in iron metabolism, by two successive methods. First, we made use of the public domain sequence data, by using assembled expressed sequence tags, non-redundant sequences, and SNP database screening. We extracted 77 potential SNPs of which only 31 could be further validated by sequencing DNA from 44 unrelated multi-ethnic individuals. Our results indicate that a bioinformatic approach may be effective only in those cases where candidate SNPs are extracted from two different data sources or in cases of experimentally confirmed SNPs. Second, additional systematic sequencing of DNA from 24 unrelated Breton subjects increased the number of SNPs over a total length of 86 kb to 96. The average distance between the SNPs and minor allele frequencies were higher than reported by others authors; this discrepancy may reflect the nature of the genes studied and the ethnic homogeneity of our test population.
引用
收藏
页码:393 / 401
页数:9
相关论文
共 34 条
[1]   Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families [J].
Adams, PC ;
Campion, ML ;
Gandon, G ;
LeGall, JY ;
David, V ;
Jouanolle, AM .
HEPATOLOGY, 1997, 26 (04) :986-990
[2]   A look at linkage disequilibrium [J].
Boehnke, M .
NATURE GENETICS, 2000, 25 (03) :246-247
[3]   Characterization of single-nucleotide polymorphisms in coding regions of human genes [J].
Cargill, M ;
Altshuler, D ;
Ireland, J ;
Sklar, P ;
Ardlie, K ;
Patil, N ;
Lane, CR ;
Lim, EP ;
Kalyanaraman, N ;
Nemesh, J ;
Ziaugra, L ;
Friedland, L ;
Rolfe, A ;
Warrington, J ;
Lipshutz, R ;
Daley, GQ ;
Lander, ES .
NATURE GENETICS, 1999, 22 (03) :231-238
[4]   RATES OF TRANSITION AND TRANSVERSION IN CODING SEQUENCES SINCE THE HUMAN-RODENT DIVERGENCE [J].
COLLINS, DW ;
JUKES, TH .
GENOMICS, 1994, 20 (03) :386-396
[5]   Polymorphisms in the HFE gene [J].
Douabin, V ;
Moirand, R ;
Jouanolle, AM ;
Brissot, P ;
Le Gall, JY ;
Deugnier, Y ;
David, V .
HUMAN HEREDITY, 1999, 49 (01) :21-26
[6]   Base-calling of automated sequencer traces using phred.: I.: Accuracy assessment [J].
Ewing, B ;
Hillier, L ;
Wendl, MC ;
Green, P .
GENOME RESEARCH, 1998, 8 (03) :175-185
[7]   The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding [J].
Feder, JN ;
Penny, DM ;
Irrinki, A ;
Lee, VK ;
Lebrón, JA ;
Watson, N ;
Tsuchihashi, Z ;
Sigal, E ;
Bjorkman, PJ ;
Schatzman, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1472-1477
[8]   A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [J].
Feder, JN ;
Gnirke, A ;
Thomas, W ;
Tsuchihashi, Z ;
Ruddy, DA ;
Basava, A ;
Dormishian, F ;
Domingo, R ;
Ellis, MC ;
Fullan, A ;
Hinton, LM ;
Jones, NL ;
Kimmel, BE ;
Kronmal, GS ;
Lauer, P ;
Lee, VK ;
Loeb, DB ;
Mapa, FA ;
McClelland, E ;
Meyer, NC ;
Mintier, GA ;
Moeller, N ;
Moore, T ;
Morikang, E ;
Prass, CE ;
Quintana, L ;
Starnes, SM ;
Schatzman, RC ;
Brunke, KJ ;
Drayna, DT ;
Risch, NJ ;
Bacon, BR ;
Wolff, RK .
NATURE GENETICS, 1996, 13 (04) :399-408
[9]   The hemochromatosis founder mutation in HLA-H disrupts beta(2)-microglobulin interaction and cell surface expression [J].
Feder, JN ;
Tsuchihashi, Z ;
Irrinki, A ;
Lee, VK ;
Mapa, FA ;
Morikang, E ;
Prass, CE ;
Starnes, SM ;
Wolff, RK ;
Parkkila, S ;
Sly, WS ;
Schatzman, RC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (22) :14025-14028
[10]   Consed: A graphical tool for sequence finishing [J].
Gordon, D ;
Abajian, C ;
Green, P .
GENOME RESEARCH, 1998, 8 (03) :195-202