Quantitative Trait Loci for Body Weight, Blood Pressure, Blood Glucose, and Serum Lipids: Linkage Analysis with Wild Rats (Rattus norvegicus)

2001 ◽  
Vol 284 (5) ◽  
pp. 1126-1133 ◽  
Author(s):  
Ingrid Klöting ◽  
Peter Kovács ◽  
Jens van den Brandt
2000 ◽  
Vol 11 (10) ◽  
pp. 824-830 ◽  
Author(s):  
Akira Ishikawa ◽  
Yoichi Matsuda ◽  
Takao Namikawa

2013 ◽  
Vol 22 (22) ◽  
pp. 4451-4459 ◽  
Author(s):  
Cristina Chauvet ◽  
Kimberley Crespo ◽  
Annie Ménard ◽  
Julie Roy ◽  
Alan Y. Deng

2008 ◽  
Vol 72 (6) ◽  
pp. 762-773 ◽  
Author(s):  
E. K. Larkin ◽  
S. R. Patel ◽  
R. C. Elston ◽  
C. Gray-McGuire ◽  
X. Zhu ◽  
...  

Genetics ◽  
2002 ◽  
Vol 160 (2) ◽  
pp. 779-792 ◽  
Author(s):  
Rongling Wu ◽  
Chang-Xing Ma ◽  
George Casella

AbstractLinkage analysis and allelic association (also referred to as linkage disequilibrium) studies are two major approaches for mapping genes that control simple or complex traits in plants, animals, and humans. But these two approaches have limited utility when used alone, because they use only part of the information that is available for a mapping population. More recently, a new mapping strategy has been designed to integrate the advantages of linkage analysis and linkage disequilibrium analysis for genome mapping in outcrossing populations. The new strategy makes use of a random sample from a panmictic population and the open-pollinated progeny of the sample. In this article, we extend the new strategy to map quantitative trait loci (QTL), using molecular markers within the EM-implemented maximum-likelihood framework. The most significant advantage of this extension is that both linkage and linkage disequilibrium between a marker and QTL can be estimated simultaneously, thus increasing the efficiency and effectiveness of genome mapping for recalcitrant outcrossing species. Simulation studies are performed to test the statistical properties of the MLEs of genetic and genomic parameters including QTL allele frequency, QTL effects, QTL position, and the linkage disequilibrium of the QTL and a marker. The potential utility of our mapping strategy is discussed.


1997 ◽  
Vol 70 (2) ◽  
pp. 117-124 ◽  
Author(s):  
KELLIE A. RANCE ◽  
WILLIAM G. HILL ◽  
PETER D. KEIGHTLEY

Evidence of a large sex-linked effect accounting for 25% of the divergence between mouse lines selected for body weight has been described previously. A marker-based study was undertaken to determine the number and map positions of the putative X-linked quantitative trait loci (QTLs). An F2 population was generated from a reciprocal F1 between an inbred low line derived from the low selection line and the high selection line. To enable inference of marker-associated QTL effects on the X chromosome, an analytical technique was developed based on the multiple regression method of Haley and Knott. The analysis of data on 10 week weight indicated a single QTL of large effect situated at about 23 cM from the proximal end of the chromosome, with a peak LOD score of 24·4. The likelihood curve showed a single well-defined peak, and gave a 95% confidence interval for the QTL location of 8 cM. The estimates for the additive genotypic effects in males and females (half the differences between hemizygous males and between homozygous females) were 2·6 g in both cases, or 17% and 20% of the 10 week body weight in males and females respectively. Dominance effects in the females were found to be non-significant. No significant X-linked effect on carcass fat percentage was detected, but a single X-linked QTL appears to explain almost the entire X-linked body weight effect.


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