A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees

被引:144
作者
McInnes, LA
Escamilla, MA
Service, SK
Reus, VI
Leon, P
Silva, S
Rojas, E
Spesny, M
Baharloo, S
Blankenship, K
Peterson, A
Tyler, D
Shimayoshi, N
Tobey, C
Batki, S
Vinogradov, S
Meza, L
Gallegos, A
Fournier, E
Smith, LB
Barondes, SH
Sandkuijl, LA
Freimer, NB
机构
[1] UNIV CALIF SAN FRANCISCO,NEUROGENET LAB,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT PSYCHIAT,SAN FRANCISCO,CA 94143
[3] UNIV COSTA RICA,ESCUELA MED,SAN JOSE,COSTA RICA
[4] UNIV COSTA RICA,CELL & MOL BIOL RES CTR,SAN JOSE,COSTA RICA
[5] UNIV CALIF SAN FRANCISCO,SAN FRANCISCO GEN HOSP,DEPT PSYCHIAT,SAN FRANCISCO,CA 94110
[6] HOSP CALDERON GUARDIA,SAN JOSE,COSTA RICA
[7] ERASMUS UNIV ROTTERDAM,DEPT CLIN GENET,NL-3000 DR ROTTERDAM,NETHERLANDS
[8] LEIDEN UNIV,DEPT HUMAN GENET,NL-2300 RA LEIDEN,NETHERLANDS
[9] UNIV GRONINGEN,DEPT MED GENET,GRONINGEN,NETHERLANDS
[10] UNIV CALIF SAN FRANCISCO,GENET PROGRAM,SAN FRANCISCO,CA 94143
[11] UNIV CALIF SAN FRANCISCO,PROGRAM BIOMED SCI,SAN FRANCISCO,CA 94143
关键词
D O I
10.1073/pnas.93.23.13060
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bipolar mood disorder (BP) is a debilitating syndrome characterized by episodes of mania and depression. We designed a multistage study to detect all major loci predisposing to severe BP (termed BP-I) in two pedigrees drawn from the Central Valley of Costa Rica, where the population is largely descended from a few founders in the 16th-18th centuries. We considered only individuals with BP-I as affected and screened the genome for linkage with 473 microsatellite markers. We used a model for linkage analysis that incorporated a high phenocopy rate and a conservative estimate of penetrance. Our goal in this study was not to establish definitive linkage but rather to detect all regions possibly harboring major genes far BP-I in these pedigrees. To facilitate this aim, we evaluated the degree to which markers that were informative in our data set provided coverage of each genome region; we estimate that at least 94% of the genome has been covered, at a predesignated threshold determined through prior linkage simulation analyses. We report here the results of our genome screen far BP-I loci and indicate several regions that merit further study, including segments in 18q, 18p, and 11p, in which suggestive lod scores were observed for two or more contiguous markers. Isolated lod scores that exceeded our thresholds in one or both families also occurred on chromosomes 1, 2, 3, 4, 5, 7, 13, 15, 16, and 17. Interesting regions highlighted in this genome screen will be followed up using linkage disequilibrium (LD) methods.
引用
收藏
页码:13060 / 13065
页数:6
相关论文
共 40 条
[1]   GENETIC-LINKAGE BETWEEN X-CHROMOSOME MARKERS AND BIPOLAR AFFECTIVE-ILLNESS [J].
BARON, M ;
RISCH, N ;
HAMBURGER, R ;
MANDEL, B ;
KUSHNER, S ;
NEWMAN, M ;
DRUMER, D ;
BELMAKER, RH .
NATURE, 1987, 326 (6110) :289-292
[2]   DIMINISHED SUPPORT FOR LINKAGE BETWEEN MANIC-DEPRESSIVE ILLNESS AND X-CHROMOSOME MARKERS IN 3 ISRAELI PEDIGREES [J].
BARON, M ;
FREIMER, NF ;
RISCH, N ;
LERER, B ;
ALEXANDER, JR ;
STRAUB, RE ;
ASOKAN, S ;
DAS, K ;
PETERSON, A ;
AMOS, J ;
ENDICOTT, J ;
OTT, J ;
GILLIAM, TC .
NATURE GENETICS, 1993, 3 (01) :49-55
[3]   CHROMOSOME-18 DNA MARKERS AND MANIC-DEPRESSIVE ILLNESS - EVIDENCE FOR A SUSCEPTIBILITY GENE [J].
BERRETTINI, WH ;
FERRARO, TN ;
GOLDIN, LR ;
WEEKS, DE ;
DETERAWADLEIGH, S ;
NURNBERGER, JI ;
GERSHON, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) :5918-5921
[4]   DANISH TWIN STUDY OF MANIC-DEPRESSIVE DISORDERS [J].
BERTELSEN, A ;
HARVALD, B ;
HAUGE, M .
BRITISH JOURNAL OF PSYCHIATRY, 1977, 130 (APR) :330-351
[5]  
BOEHNKE M, 1991, AM J HUM GENET, V48, P22
[6]   LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33 [J].
COPEMAN, JB ;
CUCCA, F ;
HEARNE, CM ;
CORNALL, RJ ;
REED, PW ;
RONNINGEN, KS ;
UNDLIEN, DE ;
NISTICO, L ;
BUZZETTI, R ;
TOSI, R ;
POCIOT, F ;
NERUP, J ;
CORNELIS, F ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE GENETICS, 1995, 9 (01) :80-85
[7]   A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J].
DAVIES, JL ;
KAWAGUCHI, Y ;
BENNETT, ST ;
COPEMAN, JB ;
CORDELL, HJ ;
PRITCHARD, LE ;
REED, PW ;
GOUGH, SCL ;
JENKINS, SC ;
PALMER, SM ;
BALFOUR, KM ;
ROWE, BR ;
FARRALL, M ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE, 1994, 371 (6493) :130-136
[8]   MUTATIONAL PROCESSES OF SIMPLE-SEQUENCE REPEAT LOCI IN HUMAN-POPULATIONS [J].
DIRIENZO, A ;
PETERSON, AC ;
GARZA, JC ;
VALDES, AM ;
SLATKIN, M ;
FREIMER, NB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3166-3170
[9]   ANALYSIS OF X-LINKAGE [J].
EDWARDS, JH .
ANNALS OF HUMAN GENETICS, 1971, 34 (FEB) :229-&
[10]   BIPOLAR AFFECTIVE-DISORDERS LINKED TO DNA MARKERS ON CHROMOSOME-11 [J].
EGELAND, JA ;
GERHARD, DS ;
PAULS, DL ;
SUSSEX, JN ;
KIDD, KK ;
ALLEN, CR ;
HOSTETTER, AM ;
HOUSMAN, DE .
NATURE, 1987, 325 (6107) :783-787