scholarly journals Prediction of prion protein genotype and association of this genotype with lamb performance traits of Suffolk sheep1,2

2010 ◽  
Vol 88 (2) ◽  
pp. 428-434 ◽  
Author(s):  
R. M. Sawalha ◽  
B. Villanueva ◽  
S. Brotherstone ◽  
P. L. Rogers ◽  
R. M. Lewis
2004 ◽  
Vol 155 (5) ◽  
pp. 140-143 ◽  
Author(s):  
F. de Vries ◽  
N. Hamann ◽  
C. Drögemüller ◽  
O. Distl ◽  
N. Borchers ◽  
...  

1995 ◽  
Vol 187 (2) ◽  
pp. 127-129 ◽  
Author(s):  
Stuart M. Pickering-Brown ◽  
David M.A. Mann ◽  
Frank Owen ◽  
James W. Ironside ◽  
Rajith de Silva ◽  
...  

2013 ◽  
Vol 37 ◽  
pp. 625-630
Author(s):  
Stelian BARAITAREANU ◽  
Maria Rodica OTELEA ◽  
Mihaela ZAULET ◽  
Kurt SCHNEIDER ◽  
Mihai TURCITU ◽  
...  

2004 ◽  
Vol 79 (3) ◽  
pp. 397-404 ◽  
Author(s):  
F. de Vries ◽  
H. Hamann ◽  
C. Drögemüller ◽  
M. Ganter ◽  
O. Distl

AbstractThe objective of this study was to analyse the associations between ovine prion protein (PrP) genotypes and reproduction traits in three German meat sheep breeds. Reproduction traits were age at first early lambing, age at first late lambing, first lambing interval, second lambing interval and total number of lambs born. The data set included 595 genotyped German Texel sheep among 5225 recorded sheep, 351 genotyped German Black-Headed Mutton among 10 177 sheep and 282 genotyped Suffolk sheep among 2849 sheep. Linear animal models were employed for the analysis of the PrP-genotype effect. The PrP-genotype effect was analysed by comparing the most frequent PrP genotypes ARR/ARR, ARR/ARQ, and ARQ/ARQ. In a more general analysis three PrP genotype classes of animals with two, one or no copy of the ARR allele were compared.In most cases, no significant associations were found between the PrP genotypes and the reproduction traits investigated. Only for the traits age at first early lambing in German Texel and second lambing interval in German Black-Headed Mutton and Suffolk could a significant association with the PrP genotype be observed.


2009 ◽  
Vol 5 (1) ◽  
pp. 3 ◽  
Author(s):  
Simon Gubbins ◽  
Charlotte J Cook ◽  
Kieran Hyder ◽  
Kay Boulton ◽  
Carol Davis ◽  
...  

1997 ◽  
Vol 93 (3) ◽  
pp. 317-322 ◽  
Author(s):  
Koichi Kawasaki ◽  
Koichi Wakabayashi ◽  
Akio Kawakami ◽  
Masami Higuchi ◽  
Tetsuyuki Kitamoto ◽  
...  

1994 ◽  
Vol 179 (1-2) ◽  
pp. 50-52 ◽  
Author(s):  
Rajith de Silva ◽  
James W Ironside ◽  
Linda McCardle ◽  
Thomas Esmonde ◽  
Jeanne Bell ◽  
...  

Nature ◽  
1991 ◽  
Vol 352 (6335) ◽  
pp. 547-547
Author(s):  
Mark S. Palmer ◽  
Aidan J. Dryden ◽  
J. Trevor Hughes ◽  
John Collinge

2004 ◽  
Vol 85 (9) ◽  
pp. 2735-2740 ◽  
Author(s):  
M. Baylis ◽  
C. Chihota ◽  
E. Stevenson ◽  
W. Goldmann ◽  
A. Smith ◽  
...  

There is a well-established association between sheep prion protein (PrP) genotype and the risk of death from scrapie. Certain genotypes are clearly associated with susceptibility to the disease and others to resistance. However, there have been no attempts to quantify the disease risk for all 15 PrP genotypes. Here, datasets of the PrP genotypes of nearly 14 000 British sheep and of more than 1500 confirmed scrapie cases were combined to yield an estimate of scrapie risk (reported cases per annum per million sheep of the genotype, or RCAM) for British sheep. The greatest scrapie risk by far, ranging from 225 to 545 RCAM, was for the VRQ-encoding genotypes ARQ/VRQ, ARH/VRQ and VRQ/VRQ. The next greatest risk (37 RCAM) was for the ARQ/ARQ genotype. The ARR/ARR genotype was the only numerically significant genotype for which no scrapie cases have been reported. The AHQ allele conferred resistance and the risk of scrapie in AHQ/VRQ sheep was very low (0·7 RCAM), although there was a higher and moderate risk for the AHQ homozygote (5 RCAM). The ARH allele appeared to confer susceptibility when encoded with VRQ, but possible resistance when encoded with other alleles. Scrapie risk varied with age: for VRQ/VRQ and ARH/VRQ the risk peaked at 2 years of age; that for ARQ/VRQ peaked at 3 years. There was some evidence that, following the lower risk at 4 and 5 years, a second rise occurred from about 6 years. Comparison with other published data indicated that the scrapie risk of certain PrP genotypes may differ between Great Britain and other countries.


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