Identification of multiple quantitative trait loci linked to prion disease incubation period in mice

被引:149
作者
Lloyd, SE
Onwuazor, ON
Beck, JA
Mallinson, G
Farrall, M
Targonski, P
Collinge, J
Fisher, EMC
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, MRC, Prion Unit, London W2 1PG, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Dept Cardiovasc Med, Oxford OX3 7BN, England
关键词
D O I
10.1073/pnas.101130398
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
Polymorphisms in the prion protein gene are known to affect prion disease incubation times and susceptibility in humans and mice. However, studies with inbred lines of mice show that large differences in incubation times occur even with the same amino acid sequence of the prion protein, suggesting that other genes may contribute to the observed variation. To identify these loci we analyzed 1,009 animals from an F2 intercross between two strains of mice, CAST/Ei and NZW/OlaHSd, with significantly different incubation periods when challenged with RML scrapie prions, Interval mapping identified three highly significantly linked regions on chromosomes 2, 11, and 12; composite interval mapping suggests that each of these regions includes multiple linked quantitative trait loci. Suggestive evidence for linkage was obtained on chromosomes 6 and 7. The sequence conservation between the mouse and human genome suggests that identification of mouse prion susceptibility alleles may have direct relevance to understanding human susceptibility to bovine spongiform encephalopathy (BSE) infection, as well as identifying key factors in the molecular pathways of prion pathogenesis. However, the demonstration of other major genetic effects on incubation period suggests the need for extreme caution in interpreting estimates of variant Creutzfeldt-Jakob disease epidemic size utilizing existing epidemiological models.
引用
收藏
页码:6279 / 6283
页数:5
相关论文
共 39 条
[1]   AMINO-ACID POLYMORPHISM IN HUMAN PRION PROTEIN AND AGE AT DEATH IN INHERITED PRION DISEASE [J].
BAKER, HF ;
POULTER, M ;
CROW, TJ ;
FRITH, CD ;
LOFTHOUSE, R ;
RIDLEY, RM ;
COLLINGE, J .
LANCET, 1991, 337 (8752) :1286-1286
[2]  
Basten C., 2000, QTL CARTOGRAPHER 1 1
[3]   Characterisation of two promoters for prion protein (PrP) gene expression in neuronal cells [J].
Baybutt, H ;
Manson, J .
GENE, 1997, 184 (01) :125-131
[4]   Genealogies of mouse inbred strains [J].
Beck, JA ;
Lloyd, S ;
Hafezparast, M ;
Lennon-Pierce, M ;
Eppig, JT ;
Festing, MFW ;
Fisher, EMC .
NATURE GENETICS, 2000, 24 (01) :23-+
[5]   Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent [J].
Bruce, ME ;
Will, RG ;
Ironside, JW ;
McConnell, I ;
Drummond, D ;
Suttie, A ;
McCardle, L ;
Chree, A ;
Hope, J ;
Birkett, C ;
Cousens, S ;
Fraser, H ;
Bostock, CJ .
NATURE, 1997, 389 (6650) :498-501
[6]  
BUELER H, 1994, MOL MED, V1, P19
[7]   LINKAGE OF PRION PROTEIN AND SCRAPIE INCUBATION-TIME GENES [J].
CARLSON, GA ;
KINGSBURY, DT ;
GOODMAN, PA ;
COLEMAN, S ;
MARSHALL, ST ;
DEARMOND, S ;
WESTAWAY, D ;
PRUSINER, SB .
CELL, 1986, 46 (04) :503-511
[8]   GENETICS AND POLYMORPHISM OF THE MOUSE PRION GENE-COMPLEX - CONTROL OF SCRAPIE INCUBATION-TIME [J].
CARLSON, GA ;
GOODMAN, PA ;
LOVETT, M ;
TAYLOR, BA ;
MARSHALL, ST ;
PETERSONTORCHIA, M ;
WESTAWAY, D ;
PRUSINER, SB .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (12) :5528-5540
[9]   Phenotype-genotype studies in kuru:: Implications for new variant Creutzfeldt-Jakob disease [J].
Cervenáková, L ;
Goldfarb, LG ;
Garruto, R ;
Lee, HS ;
Gajdusek, DC ;
Brown, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13239-13241
[10]   Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD [J].
Collinge, J ;
Sidle, KCL ;
Meads, J ;
Ironside, J ;
Hill, AF .
NATURE, 1996, 383 (6602) :685-690