The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations

被引:85
作者
Hall, D
Gogos, JA
Karayiorgou, M
机构
[1] Rockefeller Univ, Human Neurogenet Lab, New York, NY 10021 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Physiol & Cellular Biophys, New York, NY USA
[3] Columbia Univ, Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY USA
关键词
association studies; candidate genes; chromosome; 6; 8; 13; schizophrenia;
D O I
10.1111/j.1601-183X.2004.00078.x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Here we characterize and compare the contribution of three recently identified strong candidate schizophrenia susceptibility genes; G72, neuregulin 1 (NRG1) and dystrobrevin-binding protein 1 (DTNBP1) in two independent datasets of patients with distinct genetic backgrounds. On the basis of corrected P-values from single- and multilocus transmission distortion tests our analysis provides no support for a contribution of G72, NRG1 or DTNBP1 in the tested samples. When transmission of individual haplotypes was considered, a picture more consistent with the original studies emerged, where transmission distortions in the same direction as the original samples and involving the same core haplotypes were observed for G72 and NRG1. Interestingly, whereas the NRG1 gene analysis was dominated by the presence of over-transmitted haplotypes, the G72 gene analysis was consistently dominated in both datasets by under-transmissions. Negative transmissions involved a core haplotype complementary to the originally detected over-transmitted haplotype, suggesting the presence of a protective variant within the G72 locus.
引用
收藏
页码:240 / 248
页数:9
相关论文
共 36 条
[1]   Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1 [J].
Abecasis, GR ;
Burt, RA ;
Hall, D ;
Bochum, S ;
Doheny, KF ;
Lundy, SL ;
Torrington, M ;
Roos, JL ;
Gogos, JA ;
Karayiorgou, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (03) :403-417
[2]   The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes [J].
Altshuler, D ;
Hirschhorn, JN ;
Klannemark, M ;
Lindgren, CM ;
Vohl, MC ;
Nemesh, J ;
Lane, CR ;
Schaffner, SF ;
Bolk, S ;
Brewer, C ;
Tuomi, T ;
Gaudet, D ;
Hudson, TJ ;
Daly, M ;
Groop, L ;
Lander, ES .
NATURE GENETICS, 2000, 26 (01) :76-80
[3]  
[Anonymous], 1994, DIAGN STAT MAN
[4]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[5]   Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain [J].
Benson, MA ;
Newey, SE ;
Martin-Rendon, E ;
Hawkes, R ;
Blake, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :24232-24241
[6]   Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 [J].
Blouin, JL ;
Dombroski, BA ;
Nath, SK ;
Lasseter, VK ;
Wolyniec, PS ;
Nestadt, G ;
Thornquist, M ;
Ullrich, G ;
McGrath, J ;
Kasch, L ;
Lamacz, M ;
Thomas, MG ;
Gehrig, C ;
Radhakrishna, U ;
Snyder, SE ;
Balk, KG ;
Neufeld, K ;
Swartz, KL ;
DeMarchi, N ;
Papadimitriou, GN ;
Dikeos, DG ;
Stefanis, CN ;
Chakravarti, A ;
Childs, B ;
Housman, DE ;
Kazazian, HH ;
Antonarakis, SE ;
Pulver, AE .
NATURE GENETICS, 1998, 20 (01) :70-73
[7]   Modulation of non-templated nucleotide addition by taq DNA polymerase: Primer modifications that facilitate genotyping [J].
Brownstein, MJ ;
Carpten, JD ;
Smith, JR .
BIOTECHNIQUES, 1996, 20 (06) :1004-+
[8]  
Brzustowicz LM, 1999, AM J HUM GENET, V65, P1096, DOI 10.1086/302579
[9]  
Chen XN, 1999, GENOME RES, V9, P492
[10]   Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia [J].
Chumakov, I ;
Blumenfeld, M ;
Guerassimenko, O ;
Cavarec, L ;
Palicio, M ;
Abderrahim, H ;
Bougueleret, L ;
Barry, C ;
Tanaka, H ;
La Rosa, P ;
Puech, A ;
Tahri, N ;
Cohen-Akenine, A ;
Delabrosse, S ;
Lissarrague, S ;
Picard, FP ;
Maurice, K ;
Essioux, L ;
Millasseau, P ;
Grel, P ;
Debailleul, V ;
Simon, AM ;
Caterina, D ;
Dufaure, I ;
Malekzadeh, K ;
Belova, M ;
Luan, JJ ;
Bouillot, M ;
Sambucy, JL ;
Primas, G ;
Saumier, M ;
Boubkiri, N ;
Martin-Saumier, S ;
Nasroune, M ;
Peixoto, H ;
Delaye, A ;
Pinchot, V ;
Bastucci, M ;
Guillou, S ;
Chevillon, M ;
Sainz-Fuertes, R ;
Meguenni, S ;
Aurich-Costa, J ;
Cherif, D ;
Gimalac, A ;
Van Duijn, C ;
Gauvreau, D ;
Quelette, G ;
Fortier, I ;
Realson, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) :13675-13680