A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees

被引:117
作者
Lindholm, E
Ekholm, B
Shaw, S
Jalonen, P
Johansson, G
Pettersson, U
Sherrington, R
Adolfsson, R
Jazin, E
机构
[1] Univ Uppsala, Dept Genet & Pathol, S-75123 Uppsala, Sweden
[2] Umea Univ, Dept Clin Sci, Umea, Sweden
[3] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[5] Pfizer Global Res & Dev, Alameda Lab, Alameda, CA USA
关键词
D O I
10.1086/321288
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have completed a genome scan of a 12-generation, 3,400-member pedigree with schizophrenia. Samples from 210 individuals were collected from the pedigree. We performed an "affecteds-only" genome-scan analysis using 43 members of the pedigree. The affected individuals included 29 patients with schizophrenia, 10 with schizoaffective disorders, and 4 with psychosis not otherwise specified. Two sets of white-European allele frequencies were used-one from a Swedish control population (46 unrelated individuals) and one from the pedigree (210 individuals). All analyses pointed to the same region: D6S264, located at 6q25.2, showed a maximum LOD score of 3.45 when allele frequencies in the Swedish control population were used, compared with a maximum LOD score of 2.59 when the pedigree's allele frequencies were used. We analyzed additional markers in the 6q25 region and found a maximum LOD score of 6.6 with marker D6S253, as well as a 6-cM haplotype (markers D6S253-D6S264) that segregated, after 12 generations, with the majority of the affected individuals. Multipoint analysis was performed with the markers in the 6q25 region, and a maximum LOD score of 7.7 was obtained. To evaluate the significance of the genome scan, we simulated the complete analysis under the assumption of no linkage. The results showed that a LOD score > 2.2 should be considered as suggestive of linkage, whereas a LOD score > 3.7 should be considered as significant. These results suggest that a common ancestral region was inherited by the affected individuals in this large pedigree.
引用
收藏
页码:96 / 105
页数:10
相关论文
共 45 条
  • [1] Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
    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
    [J]. NATURE GENETICS, 1998, 20 (01) : 70 - 73
  • [2] BOEHNKE M, 1991, AM J HUM GENET, V48, P22
  • [3] Location of a major susceptibility locus for familiar schizophrenia on chromosome 1q21-q22
    Brzustowicz, LM
    Hodgkinson, KA
    Chow, EWC
    Honer, WG
    Bassett, AS
    [J]. SCIENCE, 2000, 288 (5466) : 678 - 682
  • [4] Brzustowicz LM, 1999, AM J HUM GENET, V65, P1096, DOI 10.1086/302579
  • [5] Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees
    Cao, QH
    Martinez, M
    Zhang, J
    Sanders, AR
    Badner, JA
    Cravchik, A
    Markey, CJ
    Beshah, E
    Guroff, JJ
    Maxwell, ME
    Kazuba, DM
    Whiten, R
    Goldin, LR
    Gershon, ES
    Gejman, PV
    [J]. GENOMICS, 1997, 43 (01) : 1 - 8
  • [6] A metric map of humans: 23,500 loci in 850 bands
    Collins, A
    Frezal, J
    Teague, J
    Morton, NE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) : 14771 - 14775
  • [7] COTTINGHAM RW, 1993, AM J HUM GENET, V53, P252
  • [8] Crowe Raymond R., 1998, Psychiatric Genetics, V8, P73
  • [9] Genome-wide scan for schizophrenia in the Finnish population:: evidence for a locus on chromosome 7q22
    Ekelund, J
    Lichtermann, D
    Hovatta, I
    Ellonen, P
    Suvisaari, J
    Terwilliger, JD
    Juvonen, H
    Varilo, T
    Arajärvi, R
    Kokko-Sahin, ML
    Lönnqvist, J
    Peltonen, L
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (07) : 1049 - 1057
  • [10] FREIMER NB, 1993, AM J HUM GENET, V52, P1102