Selection for Relationships Opposite to those predicted by the Genetic Correlation between Two Traits in the House Mouse (Mus musculus)

Nature ◽  
1959 ◽  
Vol 183 (4657) ◽  
pp. 342-343 ◽  
Author(s):  
F. COCKREM
Keyword(s):  
Genetic Correlation ◽  
House Mouse ◽  
Mus Musculus ◽  
Selection For

Early Cold Exposure: Effects on Behavioral and Physiological Thermoregulation in the House Mouse, Mus musculus

1976 ◽  
Vol 49 (2) ◽  
pp. 191-199 ◽  
Author(s):  
G. Robert Lynch ◽  
Carol Becker Lynch ◽  
Marjory Dube ◽  
Cynthia Allen
Keyword(s):  
House Mouse ◽  
Cold Exposure ◽  
Mus Musculus

scholarly journals Insights into mammalian biology from the wild house mouse Mus musculus

eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Megan Phifer-Rixey ◽  
Michael W Nachman
Keyword(s):  
House Mouse ◽  
Mus Musculus ◽  
Genetic Model ◽  
Inbred Strains ◽  
Mendelian Inheritance ◽  
Model Organisms ◽  
House Mice ◽  
Small Subset ◽  
Wild Mice ◽  
Wide Range

The house mouse, Mus musculus, was established in the early 1900s as one of the first genetic model organisms owing to its short generation time, comparatively large litters, ease of husbandry, and visible phenotypic variants. For these reasons and because they are mammals, house mice are well suited to serve as models for human phenotypes and disease. House mice in the wild consist of at least three distinct subspecies and harbor extensive genetic and phenotypic variation both within and between these subspecies. Wild mice have been used to study a wide range of biological processes, including immunity, cancer, male sterility, adaptive evolution, and non-Mendelian inheritance. Despite the extensive variation that exists among wild mice, classical laboratory strains are derived from a limited set of founders and thus contain only a small subset of this variation. Continued efforts to study wild house mice and to create new inbred strains from wild populations have the potential to strengthen house mice as a model system.

Mixed sex allocation strategies in a polytocous mammal, the house mouse (Mus musculus)

2011 ◽  
Vol 65 (12) ◽  
pp. 2209-2217 ◽  
Author(s):  
Adam Dušek ◽  
Luděk Bartoš ◽  
František Sedláček
Keyword(s):  
House Mouse ◽  
Mus Musculus ◽  
Sex Allocation ◽  
Allocation Strategies ◽  
Polytocous Mammal

scholarly journals Epigenetic polymorphism in wild populations of Mus musculus

1963 ◽  
Vol 4 (2) ◽  
pp. 193-220 ◽  
Author(s):  
R. J. Berry
Keyword(s):  
House Mouse ◽  
Mus Musculus ◽  
Stabilizing Selection ◽  
British Isles ◽  
Wild Populations ◽  
Local Populations ◽  
The World ◽  
Different Populations ◽  
Different Parts

It has been suggested (Berry & Searle, 1963) that the discontinuous (‘quasi-continuous’) variants studied by Grüneberg et al. in the skeleton of rodents can be regarded as constituting epigenetic polymorphism in different populations. Comparisons have been made between the incidences of skeletal variants in house mouse populations collected from: corn ricks on a single farm in Hampshire; eleven separated localities in different parts of the British Isles; and nine other places throughout the world. These showed that the method could profitably be used for genetically characterizing and hence comparing populations. There was evidence suggestive of genetical drift between local populations and stabilizing selection over a larger area.

scholarly journals Genetic correlation between traits in the ESALQ-PB1 maize population divergently selected for tassel size and ear height

2001 ◽  
Vol 58 (1) ◽  
pp. 119-123 ◽  
Author(s):  
Austeclínio Lopes Farias Neto ◽  
José Branco de Miranda Filho
Keyword(s):  
Genetic Correlation ◽  
Correlation Coefficients ◽  
Divergent Selection ◽  
Phenotypic Correlation ◽  
Base Population ◽  
Branch Number ◽  
Maize Population ◽  
Tassel Branch Number ◽  
Ear Height ◽  
Selection For

Full-sib and selfed (S1) progenies were obtained from sub-populations of ESALQ-PB1, divergently selected for tassel size (T+ and T-) and ear height (E+ and E-), and used for estimating genetic and phenotypic correlation coefficients between traits. The analyzed traits were: EW- total ear weight (g/plant), PH- plant height (cm), EH- ear height (cm), TB- tassel branch number and TL- tassel length. The highest genetic (rG) and phenotypic (rF) correlation was observed for the combination PH x EH, as expected, with average of 0.800 and 0.778, respectively over sub-populations and locations. It is apparent that divergent selection for tassel size did not affect greatly the correlation between PH and EH in the full sib progenies, but in the inbred progenies the correlation was smaller in the sub-population selected for larger tassels. Genetic correlation between PH and EH with tassel traits was always positive but ranged from 0.020 to 0.668 in Piracicaba and from 0.06 to 0.309 in Rio Verde. Genetic correlation between PH and EH with yield (EW) also was positive in the range of 0.087 to 0.503. EH showed higher correlation with EW in relation to PH x EW and differences were larger in the sub-populations divergently selected for ear height. Correlation between tassel traits with other traits was positive in most of instances and a lack of consistency was observed among sub-populations. Generally the coefficients of genetic and phenotypic correlation differed substantially from the estimates in the base population ESALQ-PB1 before divergent selection for tassel size and ear placement. Divergent selection affected the correlation between traits under unpredicted and varying magnitudes.

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