Mw. Tess et Md. Macneil, EVALUATION OF CYTOPLASMIC GENETIC-EFFECTS IN MILES CITY LINE-1 HEREFORD CATTLE, Journal of animal science, 72(4), 1994, pp. 851-856
Mixed-model techniques were used to evaluate the importance of cytopla
smic genetic effects on growth traits in beef cattle. The data used we
re records on birth weight (BWT, n = 4,716), preweaning average daily
gain (PREADG, n = 4,428), and postweaning average daily gain (POSTADG,
n = 3,476) collected from 1935 through 1989 in a closed line of Heref
ord cattle (Miles City Line 1). Selection criterion was adjusted yearl
ing weight. Cytoplasmic genetic effects were evaluated as both potenti
al fixed and random genetic effects. Cytoplasmic sources (n = 26) were
determined based on the foundation female in the maternal lineage of
each animal. All foundation females were at least five generations rem
oved from any descendant that produced a performance record. An animal
model was used to account for all nuclear additive genetic variation
among animals. Direct additive effects were estimated for all traits.
Maternal additive and permanent environmental effects were estimated f
or BWT and PREADG. Fixed effects included year of birth, age of dam, s
ex of calf, and regressions on inbreeding of calf, inbreeding of dam,
and age off postweaning gain test (POSTADG only). When cytoplasm was f
it as a fixed effect, F-tests for cytoplasmic effects were not signifi
cant (P = .10 to .99) for any trait. Inclusion of cytoplasmic source (
fixed) in the statistical model reduced residual standard deviations l
ess than .1%. Variance components for cytoplasmic genetic effects were
estimated simultaneously with variance components for direct, materna
l, direct-maternal covariance, and maternal permanent environment usin
g REML techniques. Cytoplasmic source accounted for .40, .00, and .00%
of the phenotypic variance for BWT, PREADG, and POSTADG, respectively
. These results suggest that cytoplasmic genetic effects are not impor
tant sources of variation for growth traits in beef cattle.