THE DISEASE CHARACTERISTICS OF DIFFERENT STRAINS OF SCRAPIE IN SINC CONGENIC MOUSE LINES - IMPLICATIONS FOR THE NATURE OF THE AGENT AND HOST CONTROL OF PATHOGENESIS

被引:342
作者
BRUCE, ME
MCCONNELL, I
FRASER, H
DICKINSON, AG
机构
关键词
D O I
10.1099/0022-1317-72-3-595
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mouse lines which are congenic for Sinc, the major gene controlling scrapie incubation period, have been produced by selective breeding from the inbred C57BL(Sinc(s7)) and VM(Sinc(p7)) strains; the s7 allele of Sinc has been introduced into a VM background by 18 serial backcrosses, at each generation selecting on the basis of the incubation period with the ME7 scrapie strain. The characteristics of the disease produced by seven scrapie strains have been compared in Sinc(s7) and Sinc(p7) congenic mice and in the F1 cross between them. As previously found in non-congenic mice, each scrapie strain has a characteristic, precisely reproducible incubation period pattern in the three Sinc genotypes. The Sinc gene controls the incubation period for all scrapie strains tested but the direction of allelic action and the apparent dominance pattern differs between scrapie strains. Comparison with non-congenic mice shows that other genes also have a minor effect on incubation period. The distribution of vacuolar degeneration in the brain depends mainly on the scrapie strain but is also influenced by Sinc and other unspecified mouse genes. Restriction fragment length polymorphism analysis has already shown that the close linkage between Sinc and the gene encoding PrP has been maintained in the Sinc congenic lines, strengthening the possibility that PrP is the Sinc gene product. The present study confirms that scrapie strains carry information which is independent of the host but nevertheless suggests that host PrP protein interacts with this information to regulate the progression of the disease.
引用
收藏
页码:595 / 603
页数:9
相关论文
共 58 条
[1]   PREDICTED SECONDARY STRUCTURE AND MEMBRANE TOPOLOGY OF THE SCRAPIE PRION PROTEIN [J].
BAZAN, JF ;
FLETTERICK, RJ ;
MCKINLEY, MP ;
PRUSINER, SB .
PROTEIN ENGINEERING, 1987, 1 (02) :125-135
[2]   IDENTIFICATION OF A PROTEIN THAT PURIFIES WITH THE SCRAPIE PRION [J].
BOLTON, DC ;
MCKINLEY, MP ;
PRUSINER, SB .
SCIENCE, 1982, 218 (4579) :1309-1311
[3]  
BOLTON DC, 1988, CIBA F SYMP, V135, P164
[4]   GENETIC-CONTROL OF AMYLOID PLAQUE PRODUCTION AND INCUBATION PERIOD IN SCRAPIE-INFECTED MICE [J].
BRUCE, ME ;
DICKINSON, AG .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1985, 44 (03) :285-294
[5]   CEREBRAL AMYLOIDOSIS IN SCRAPIE IN MOUSE - EFFECT OF AGENT STRAIN AND MOUSE GENOTYPE [J].
BRUCE, ME ;
DICKINSON, AG ;
FRASER, H .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1976, 2 (06) :471-478
[6]   BIOLOGICAL EVIDENCE THAT SCRAPIE AGENT HAS AN INDEPENDENT GENOME [J].
BRUCE, ME ;
DICKINSON, AG .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :79-89
[7]   PRECISE TARGETING OF THE PATHOLOGY OF THE SIALOGLYCOPROTEIN, PRP, AND VACUOLAR DEGENERATION IN MOUSE SCRAPIE [J].
BRUCE, ME ;
MCBRIDE, PA ;
FARQUHAR, CF .
NEUROSCIENCE LETTERS, 1989, 102 (01) :1-6
[8]   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
[9]   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
[10]   PRECLINICAL CHANGES IN WEIGHT OF SCRAPIE-INFECTED MICE AS A FUNCTION OF SCRAPIE AGENT-MOUSE STRAIN COMBINATION [J].
CARP, RI ;
CALLAHAN, SM ;
SERSEN, EA ;
MORETZ, RC .
INTERVIROLOGY, 1984, 21 (02) :61-69