Genetic parameter estimates for serum insulin-like growth factor I concentrations, and body weight and weight gains in Angus beef cattle divergently selected for serum insulin-like growth factor I concentration

Data for the current study were obtained from a divergent selection experiment in which the selection criterion was the average serum IGF-I concentrations of 3 postweaning blood samples collected from purebred Angus calves. Multiple-trait derivative-free REML procedures were used to obtain genetic parameter estimates for IGF-I concentrations and for BW and BW gains measured from birth to the conclusion of a 140-d postweaning performance test. Included in the analysis were 2,674 animals in the A(-1) matrix, 1,761 of which had valid records for IGF-I concentrations. Direct heritability estimates +/- SE for IGF-I concentration at d 28, 42, and 56 of the postweaning period and for mean IGF-I concentrations were 0.44 +/- 0.07, 0.51 +/- 0.08, 0.42 +/- 0.07, and 0.52 +/- 0.08, respectively. Heritability estimates for maternal genetic effects ranged from 0.10 +/- 0.05 to 0.20 +/- 0.06. The proportion of total phenotypic variance due to the maternal permanent environmental effect was essentially zero for all measures of IGF-I concentrations. Genetic correlations of IGF-I concentrations with weaning and post-weaning BW ranged from 0.07 +/- 0.12 to 0.32 +/- 0.11 and generally demonstrated an increasing trend during the postweaning period. Averaged across the various measures of IGF-I, the genetic correlation of IGF-I with preweaning gain was 0.14, whereas the genetic correlation with postweaning gain was 0.29. Genetic correlations between IGF-I and BW gain were positive during all time intervals, except between weaning and the beginning of the postweaning test and from d 84 to 112 of the postweaning period. Environmental and phenotypic correlations of IGF-I with BW and BW gains were generally positive, but small. These results indicate that postweaning serum IGF-I concentration is moderately to highly heritable and has small positive genetic, environmental, and phenotypic correlations with BW other than birth weight and with pre- and postweaning gain. Therefore, if IGF-I proves to be a biological indicator of an economically important trait (e.g., efficiency of feed use for growth) in beef cattle, it should be possible to rapidly change IGF-I concentrations via selection without significantly altering live weight or rate of gain.     

Investigation of genotype x country interactions for growth traits in beef cattle

The importance of genotype x country interactions for weaning and birth weight and postweaning gain between Argentina (AR), Canada (CA), Uruguay (UY), and the United States (US) for populations of Hereford cattle was investigated. Three sample data sets of computationally manageable sizes were formed for each trait and pairwise combination of countries to investigate possible interactions. Parameters were estimated for each sample data set via an accelerated EM-REML algorithm and multiple-trait animal models that considered either weaning or birth weight as a different trait in each country. Direct and maternal (in parentheses) weaning weight genetic correlation estimates for AR-CA, AR-UY, AR-US, CA-UY, CA-US, and UY-US were 0.82 (0.80), 0.81 (0.72), 0.81 (0.79), 0.83 (0.78), 0.85 (0.82), and 0.86 (0.81), respectively. Direct and maternal (in parentheses) birth weight genetic correlation estimates were 0.92 (0.62), 0.97, (0.85), and 0.99 (0.97) for AR-CA, AR-US, and CA-US, respectively. Birth weight was not analyzed for UY due to small amounts of data. Postweaning gain in CA and US was 160-d gain, and in AR and UY 345-d gain was used. Across-country direct genetic correlations for postweaning gain were estimated for each pairwise country data set using a model that considered weaning weight as the same trait across each country, whereas postweaning gain was treated as a different trait in each country. Direct genetic correlation estimates for postweaning gain for AR-CA, AR-UY, AR-US, CA-UY, CA-US, and US-UY were 0.64, 0.80, 0.51, 0.84, 0.92, and 0.83, respectively. The overall results indicate that weaning and birth weights of Hereford calves can be analyzed as the same trait in all countries with a common set of heritabilities and genetic correlations, after adjustment for heterogenous phenotypic variances across countries. Postweaning gain in CA and US can be considered as the same trait and analyzed using a single set of parameters. Postweaning gain in AR and UY should be considered as a separate trait from postweaning gain in CA and US, and postweaning gain in AR and UY can be considered as the same trait and analyzed using a common heritability, after adjustment for phenotypic variance differences between the two countries.     

Approximation of reliabilities for multiple-trait model with maternal effects

Reliabilities for a multiple-trait maternal model were obtained by combining reliabilities obtained from single-trait models. Single-trait reliabilities were obtained using an approximation that supported models with additive and permanent environmental effects. For the direct effect, the maternal and permanent environmental variances were assigned to the residual. For the maternal effect, variance of the direct effect was assigned to the residual. Data included 10,550 birth weight, 11,819 weaning weight, and 3,617 postweaning gain records of Senepol cattle. Reliabilities were obtained by generalized inversion and by using single-trait and multiple-trait approximation methods. Some reliabilities obtained by inversion were negative because inbreeding was ignored in calculating the inverse of the relationship matrix. The multiple-trait approximation method reduced the bias of approximation when compared with the single-trait method. The correlations between reliabilities obtained by inversion and by multiple-trait procedures for the direct effect were 0.85 for birth weight, 0.94 for weaning weight, and 0.96 for postweaning gain. Correlations for maternal effects for birth weight and weaning weight were 0.96 to 0.98 for both approximations. Further improvements can be achieved by refining the single-trait procedures.     

Cytoplasmic effects on selection response for increased growth rate in mice

To determine if cytoplasmic effects have contributed to long-term selection response for increased growth rate in mice, reciprocal cross matings were made between an unselected control line (ICR) and a line (M16) derived from ICR by long-term selection for high postweaning weight gain from 3 to 6 wk of age. Embryos were recovered 2 to 4 d following mating and transferred to pseudopregnant F1 (DBA/2NCrlBR X C57BL/6NCrlBR) females. Thus, all embryos developed in similar uterine and postnatal maternal environments. A total of 122 M16 X ICR and 123 ICR X M16 mice was produced, representing 19 litters from each cross. Litters were standardized at birth to five to seven pups. Litter weights at birth and 1 wk were recorded. Body weights at 2, 3, 4, 5 and 6 wk and weight gain from 3 to 6 wk were obtained. Weights of liver, kidneys, and sc and epididymal fat pads of males were obtained at 6 wk. Females were mated at 8 wk, and litter size at birth was recorded. Least-squares procedures were used to test for differences between reciprocal crosses for all traits. Body weight at 4 wk was higher (P less than .05) for mice with ICR cytoplasm. No other significant differences were detected. There was no evidence that cytoplasmic effects influenced direct or correlated responses to long-term selection for increased postweaning weight gain.     

Experimental selection for calving ease and postnatal growth in seven cattle populations. I. Changes in estimated breeding values

Selection was used to create select and control lines within 4 purebred and 3 composite cattle populations. Both lines were selected for similar direct yearling weight and maternal weaning weight EBV. Select lines were selected for lower 2-yr-old heifer calving difficulty score EBV and control lines were selected for average birth weight EBV. Select (n = 6,926) and control (n = 2,043) line calves were born from 1993 through 1999 and selection began with the 1992 mating. High replacement rates resulted in 2,188 births to select line and 598 births to control line heifers. Data used to calculate EBV came from these populations and from 15 yr of data preceding the experiment. Calving difficulty was scored from 1 (no assistance) to 7 (cesarean). Calving difficulty scores from all twins, malpresentations, and cows 3 yr old and older were eliminated. Except for the first year, when a single-trait BLUP was used, a multiple-trait BLUP was used to calculate direct and maternal EBV for calving difficulty score, birth weight, and weaning weight, and direct EBV for postweaning gain. Sires (n = 498) were selected from those born in both the preceding populations and the select and control lines. In purebred populations, some industry sires (n = 88) were introduced based on their EPD. Tests of mean select and control line EBV differences of calves born in the final 2 yr were based on population variation. Select line direct EBV were 1.06 lower for heifer calving difficulty score (P < 0.001) and 3.5 kg lower (P < 0.001) for birth weight than controls. Average differences for other EBV were small and not significant. Yearling weight EBV was intentionally increased in both select and control lines of purebred populations. Angus, Hereford, Charolais, and Gelbvieh yearling weight EBV in control lines increased by 32.4, 27.2, 21.0, and 10.5 kg, respectively, from 1991 and 1992 to 1998 and 1999 compared with an average increase of 2.7 kg in composite populations. Birth weight direct EBV in purebred control lines increased by approximately 8% of yearling weight EBV increases. Selection based on a multiple-trait BLUP was able to create lines differing in calving difficulty score and birth weight EBV, but not in weaning weight and postweaning gain EBV. Differences between lines should be useful for evaluating BLUP and other traits and for identifying potential limitations of genetically decreasing calving difficulty score and birth weight.     

Genetic response to selection for weaning weight or yearling weight or yearling weight and muscle score in Hereford cattle: efficiency of gain, growth, and carcass characteristics

An experiment involving crosses among selection and control lines was conducted to partition direct and maternal additive genetic response to 20 yr of selection for 1) weaning weight, 2) yearling weight, and 3) index of yearling weight and muscle score. Selection response was evaluated for efficiency of gain, growth from birth through market weight, and carcass characteristics. Heritability and genetic correlations among traits were estimated using animal model analyses. Over a time-constant interval, selected lines were heavier, gained more weight, consumed more ME, and had more gain/ME than the control. Over a weight-constant interval, selected lines required fewer days, consumed less ME, had more efficient gains, and required less energy for maintenance than control. Direct and maternal responses were estimated from reciprocal crosses among unselected sires and dams of control and selection lines. Most of the genetic response to selection in all three lines was associated with direct genetic effects, and the highest proportion was from postweaning gain. Indirect responses of carcass characteristics to selection over the 20 yr were increased weight of carcasses that had more lean meat, produced with less feed per unit of gain. At a constant carcass weight, selected lines had 1.32 to 1.85% more retail product and 1.62 to 2.24% less fat trim and 10/100 to 25/100 degrees less marbling than control. At a constant age, heritability of direct and maternal effects and correlations between them were as follows: market weight, 0.36, 0.14, and 0.10; carcass weight, 0.26, 0.15, and 0.03; longissimus muscle area, 0.33, 0.00, and 0.00; marbling, 0.36, 0.07, and -0.35; fat thickness, 0.41, 0.05, and -0.18; percentage of kidney, pelvic, and heart fat, 0.12, 0.08, and -0.76; percentage of retail product, 0.46, 0.05, and -0.29; retail product weight, 0.44, 0.08, -0.14; and muscle score, 0.37, 0.14, and -0.54. Selection criteria in all lines improved efficiency of postweaning gain and increased the amount of salable lean meat on an age- or weight-constant basis, but carcasses had slightly lower marbling scores.     

Genetic variation and covariation for growth,parasite resistance and heat tolerance in tropical cattle

Genetic parameters for growth, parasite resistance and heat tolerance in zebu-cross cattle in a tropical environment were estimated by restricted maximum likelihood procedures using various forms of an animal model. Heritability estimates for direct additive genetic effects for liveweights at birth, weaning, 12 and 18 months were 0.61, 0.20, 0.25 and 0.26, respectively and corresponding maternal additive genetic effects were 0.11, 0.32, 0.20 and 0.09. Estimates of genetic correlations between direct and maternal additive genetic effects were zero. Weight gains during the dry season were genetically uncorrelated or slightly negatively correlated to birth weight, preweaning weight gain or gains during the wet season. Heritability estimates for rectal temperature, numbers of ticks, buffalo flies and worms were 0.19, 0.34, 0.06 and 0.28, respectively, with corresponding repeatability estimates of 0.23, 0.45, 0.06 and 0.29. Phenotypic correlations between adaptive traits (heat tolerance and parasite resistance) and growth traits were low. Genetic correlations between growth and rectal temperature were negative. Genetic correlations of growth traits with worm and fly burdens were positive and with tick burdens were zero. It was concluded that in reasonably adapted genotypes, selection for growth in the Australian tropics would result in improved heat tolerance and reduced resistance to parasites. The effect of genotype on parameter estimates is discussed.     

Genetic (co)variances for calving difficulty score in composite and parental populations of beef cattle: II. Reproductive, skeletal, and carcass traits

There is limited genetic information relating calving difficulty and body weights to other productive and reproductive traits. Such information is useful for specifying selection criteria and for predicting economic consequences of selection. Genetic, maternal, and environmental covariances of six productive and reproductive measurements with calving difficulty, birth weight, 200-d weight, and 168-d postweaning gain were estimated in 12 experimental populations of cattle. Calf (direct) genetic effects resulting in longer gestation length were associated with increased calving difficulty and birth weight. Maternal genetic effects of increased gestation length and heavier birth weight were significantly associated. Lighter birth weight and reduced calving difficulty were associated with earlier heifer age at puberty. Increases in direct genetic effects of calving difficulty, 200-d weight, and postweaning gain were associated with a small increase in direct effect of scrotal circumference. Increased direct genetic effects of scrotal circumference were correlated with maternal effects decreasing calving difficulty and increasing 200-d weight. Direct effects of the skeletal measurements, yearling hip height, and heifer pelvic area were positively correlated with direct effects of calving difficulty, birth weight, 200-d weight, and postweaning gain, positively correlated with maternal effects for birth weight and 200-d weight, and negatively correlated with maternal calving difficulty. Percentage of retail product was positively associated with calving difficulty and negatively associated with 168-d gain. Predicted genetic change in calving difficulty resulting from one standard deviation of selection for either calving difficulty score or birth weight was much larger than for any other traits. Selection for 200-d weight, 168-d postweaning gain, hip height, pelvic area, or scrotal circumference was predicted to have opposite effects on direct and maternal calving difficulty. Estimated genetic correlations indicate some small to moderate relationships between calving difficulty and the measured productive and reproductive traits. However, selection for reduced calving difficulty should be based on calving difficulty score and(or) birth weight because of their superiority in predicted genetic change.     

Influence of litter size and creep feeding on preweaning gain and influence of preweaning growth on growth to slaughter in barrows

The importance of birth-to-weaning average daily gain as a determinant of weight at a final age and yield of marketable pork was investigated. Treatments were imposed to create variation in birth-to-weaning ADG independent of birth weight. Newborn pigs were cross-fostered to create litters of four through 14 pigs/litter. Creep feed was offered to pigs from 5 d of age or during last 2 d before weaning at 13 to 20 d (average = 17 d). Growth rate and carcass dissection data were obtained from 195 barrows that were slaughtered at an average age of 170 d (SD = 7.5), weight of 109 kg (SD = 10.5). All traits measured were influenced by birth dam and sire (P < 0.01). Quadratic and cubic effects (P < 0.09) of litter size on birth-to-weaning ADG and weaning weight were different between the creep feeding treatments. Data revealed a positive influence (P < 0.04) of creep feeding from 5 d of age on birth-to-weaning ADG and weaning weight in larger size (> 8) litters. Importance of the independent variables birth weight, birth-to-weaning ADG, weaning weight, and birth weight plus birth-to-weaning ADG in determination of measures of postweaning growth and yield of marketable pork were examined by step-down regression analysis. Initial models included the linear and quadratic effects of the independent variables. In general, R2 for models ranked birth weight < birth-to-weaning ADG < d-17 weaning weight < birth weight + birth-to-weaning ADG. The R2 of models for BW at 170 d of age were 0.11 (P < 0.01) using birth weight as the independent variable, 0.16 (P < 0.01) using birth-to-weaning ADG, 0.19 (P < 0.01) using d-17 weaning weight, and 0.21 (P < 0.01) using birth weight + birth-to-weaning ADG. The model for effect of birth-to-weaning ADG on BW at 170 d of age indicated that a 10-g advantage in birth-to-weaning ADG produced a 0.94-kg advantage in BW at 170 d of age. Positive relationships (P < 0.05) between birth-to-weaning ADG and measures of postweaning growth and carcass yield suggest management practices that increase birth-to-weaning ADG may be advantageous in pork production.     

Correlated responses of pre- and postweaning growth and backfat thickness to six generations of selection for ovulation rate or prenatal survival in French Large White pigs

Correlated effects of selection for components of litter size on growth and backfat thickness were estimated using data from 3 pig lines derived from the same base population of Large White. Two lines were selected for 6 generations on either high ovulation rate at puberty (OR) or high prenatal survival corrected for ovulation rate in the first 2 parities (PS). The third line was an unselected control (C). Genetic parameters for individual piglet BW at birth (IWB); at 3 wk of age (IW3W); and at weaning (IWW); ADG from birth to weaning (ADGBW), from weaning to 10 wk of age (ADGPW), and from 25 to 90 kg of BW (ADGT); and age (AGET) and average backfat thickness (ABT) at 90 kg of BW were estimated using REML methodology applied to a multivariate animal model. In addition to fixed effects, the model included the common environment of birth litter, as well as direct and maternal additive genetic effects as random effects. Genetic trends were estimated by computing differences between OR or PS and C lines at each generation using both least squares (LS) and mixed model (MM) methodology. Average genetic trends for direct and maternal effects were computed by regressing line differences on generation number. Estimates of direct and maternal heritabilities were, respectively, 0.10, 0.12, 0.20, 0.24, and 0.41, and 0.17, 0.33, 0.32, 0.41, and 0.21 (SE = 0.03 to 0.04) for IWB, IW3W, IWW, ADGBW, and ADGPW. Genetic correlations between direct and maternal effects were moderately negative for IWB (-0.21 +/- 0.18), but larger for the 4 other traits (-0.59 to -0.74). Maternal effects were nonsignificant and were removed from the final analyses of ADGT, AGET, and ABT. Direct heritability estimates were 0.34, 0.46, and 0.21 (SE = 0.03 to 0.05) for ADGT, AGET, and ABT, respectively. Direct and maternal genetic correlations of OR with performance traits were nonsignificant, with the exception of maternal correlations with IWB (-0.28 +/- 0.13) and ADGPW (0.23 +/- 0.11) and direct correlation with AGET (-0.23 +/- 0.09). Prenatal survival also had low direct but moderate to strong maternal genetic correlations (-0.34 to -0.65) with performance traits. The only significant genetic trends were a negative maternal trend for IBW in the OR line and favorable direct trends for postweaning growth (ADGT and AGET) in both lines. Selection for components of litter size has limited effects on growth and backfat thickness, although it slightly reduces birth weight and improves postweaning growth.     

Heterosis retained in advanced generations of crosses among Angus and Hereford cattle

Data from 1,909 purebred, F1, backcross and F2 and F3 inter se combinations of Angus and Hereford were used to estimate average individual, maternal and grandmaternal genetic effects, individual and maternal heterosis, dominance and epistatic genetic effects. Models for evaluating heterosis and epistatic or recombination effects were discussed. Average individual effects indicate that Angus, compared with Hereford, had calves that were born earlier, had lighter birth weights, lower pre- and postweaning gains and lower pregnancy rates. Angus also produced lighter weight carcasses with more fat cover and marbling. Maternal effects of Angus were in the direction of reduced birth weight, greater calving ease, higher preweaning but lower postweaning growth rate and increased fatness when contrasted with Hereford. There was a tendency for opposite direction of maternal and grandmaternal effects for traits influenced by preweaning maternal environment. When additive X additive effects were ignored, total heterosis was significant for earlier day born, heavier birth weight, preweaning and postweaning gain, and heavier and fatter carcasses. Heterosis retained in F3 inter se vs F1 generation crosses indicated that net epistatic effects were relatively negligible for date of calving, birth weight, weaning gain and fat cover. There was a greater reduction of heterosis effects than expected from dominance alone for survival, pregnancy and marbling score. Loss of heterosis in F3 was less than expected for postweaning gain, carcass weight and rib eye area. Except for survival, pregnancy and marbling, these deviations from dominance expectations, or lack of them, are favorable for F3 composite populations.     

Genetic and environmental growth trait parameter estimates for Brahman and Brahman-derivative cattle

Beefmaster, Brahman, Brangus, and Santa Gertrudis field data records were used to determine genetic and environmental parameter estimates using a multiple-trait, pseudo-expectation approach. Adjusted birth weight, 205-d weight, and postweaning gain records were analyzed for each breed. Also, Brangus weaning sheath and navel scores were both analyzed using a single-trait, pseudo-expectation method to determine genetic parameter estimates. Additive birth weight heritability (h2A) estimates ranged from .22 to .37 and maternal birth weight heritability (h2M) estimates ranged from .12 to .55. Estimates for 205-d weight h2A for the four breeds varied from .21 to .25, and 205-d weight h2M estimates ranged from .15 to .21. Postweaning gain h2A estimates ranged from .16 to .56. The genetic correlation between direct and maternal portions of birth weight was negative for all breeds. This was also true for the genetic correlation between direct and maternal portions of 205-d weight, except in Brahman cattle, for which it was .15. The genetic correlation between additive portions of birth weight and 205-d weight was large and positive in all breeds. A moderately positive correlation between 205-d weight and postweaning gain was found for all breeds except Santa Gertrudis, whereas the environmental correlation between these two traits was a small to moderately negative estimate in all breeds. Brangus weaning sheath and navel score heritabilities indicated that genetic change for the size and shape of the sheath and navel area is possible.     

Genetic (co)variances for calving difficulty score in composite and parental populations of beef cattle: I. Calving difficulty score, birth weight, weaning weight, and postweaning gain

Heritability of 2-yr-old heifer calving difficulty score was estimated in nine purebred and three composite populations with a total of 5,986 calving difficulty scores from 520 sires and 388 maternal grandsires. Estimates were 0.43 for direct (calf) genetic effects and 0.23 for maternal (heifer) genetic effects. The correlation between direct and maternal effects was -0.26. Direct effects were strongly positively correlated with birth weight and moderately correlated with 200-d weight and postweaning gain. Smaller negative correlations of maternal calving difficulty with direct effects of birth weight, weaning weight, and postweaning gain were estimated. Calving difficulty was scored from 1 to 7. Predicted heritabilities using seven optimal scores were similar to those using four scores. The predicted heritability using only two categories was reduced 23%. Phenotypic and direct genetic variance increased with increasing average population calving difficulty score. The estimated direct and maternal heritabilities for 2-yr-old calving difficulty score were larger than many literature estimates. These estimates suggested substantial variance for direct and maternal genetic effects. The direct effects of 2-yr-old calving difficulty score seemed to be much more closely tied to birth weight than were maternal effects.     

Maternal influence on growth of laboratory rats

Data from 2,089 laboratory rats utilized in selection experiments were used to estimate maternal influence on growth from weaning (21 d) to 16 wk of age. Adjustment factors were calculated for the effects of sex, generation, litter size, inbreeding of the dam and inbreeding of the offspring on the body weights. The effect of line of sire was included in the analysis of variance models. Covariances among paternal half-sibs, full-sibs, offspring-dam, and individuals with the same maternal grandsire were equated to theoretical causal components of variance in a series of simultaneous equations. From these, estimates of heritability, maternal influence and other environmental influences on the weights of the animals were calculated. Estimates of additive genetic effects were negative at weaning and increased to positive intermediate values during postweaning growth. Maternal influence due to additive genetic effects was of primary importance at weaning and tended to diminish at later stages of growth. An antagonism was indicated between maternal environment and genes affecting the offspring's growth. Maternal influence is an important factor at weaning and during the postweaning growth of a litter-bearing species such as the laboratory rat.     

Genetic analysis of absolute growth measurements, relative growth rate and restricted selection indices in red Angus cattle

Performance records on 41,184 Red Angus cattle were analyzed and estimates of parameters calculated for absolute growth rate, relative growth rate and restricted selection indices. Heritability estimates for birth weight, 205-d weight, 365-d weight and postweaning gain were .46 +/- .02, .39 +/- .02, .40 +/- .02 and .36 +/- .02, respectively. Heritability estimates for preweaning, postweaning and postnatal relative growth rates were identical (.33 +/- .02). Heritability estimates for restricted selection indices were .31 +/- .02, .33 +/- .02 and .31 +/- .02 for weaning index, yearling index and postweaning index, respectively. The genetic correlation between preweaning and postweaning absolute growth rate was .15. The genetic correlation between consecutive measurements of relative growth rate (RGR) was -.33. Genetic correlations of birth weight with preweaning RGR and postnatal RGR were -.68 and -.71, respectively. Correlations among measures of relative growth rate using simulated data were similar to correlations of actual data, indicating that these relationships are the result of numerator/denominator relationships and not biological causes. The genetic correlation between weaning and postweaning indices was near zero. Small genetic coefficients of variation for preweaning and postnatal relative growth rates indicate further problems with the expression of growth in this manner. Restricted selection indices exhibited much larger genetic coefficients of variation than measurements of RGR. Genetic standard deviations were 7.8%, 7.2% and 13.7% of the means for weaning, yearling and postweaning indices, respectively.     

Effects of divergent selection for serum insulin-like growth factor-I concentration on performance, feed efficiency, and ultrasound measures of carcass composition traits in Angus bulls and heifers

Angus bulls and heifers from lines divergently selected for serum IGF-I concentration were used to evaluate the effects of IGF-I selection line on growth performance and feed efficiency in 2 studies. In study 1, bulls (low line, n = 9; high line, n = 8; initial BW = 367.1 +/- 22.9 kg) and heifers (low line, n = 9; high line, n = 13; initial BW = 286.4 +/- 28.6 kg) were adapted to a roughage-based diet (ME = 1.95 Mcal/kg of DM) for 24 d and fed individually for 77 d by using Calan gate feeders. In study 2, bulls (low line, n = 15; high line, n = 12; initial BW = 297.5 +/- 34.4 kg) and heifers (low line, n = 9; high line, n = 20; initial BW = 256.0 +/- 25.1 kg) were adapted to a grain-based diet (ME = 2.85 Mcal/kg of DM) for 32 d and fed individually for 70 d by using Calan gate feeders. Blood samples were collected at weaning and at the start and end of each study, and serum IGF-I concentration was determined. Residual feed intake (RFI) was calculated, within study, as the residual from the linear regression of DMI on midtest BW(0.75), ADG, sex, sex by midtest BW(0.75) and sex by ADG. In study 1, calves from the low IGF-I selection line had similar initial and final BW and ADG, compared with calves from the high IGF-I selection line. In addition, DMI and feed conversion ratio were similar between IGF-I selection lines; however, calves from the low IGF-I selection line tended (P < 0.10) to have lesser RFI than calves from the high IGF-I selection line (-0.26 vs. 0.24 +/- 0.31 kg/d). In study 2, IGF-I selection line had no influence on performance or feed efficiency traits. However, there was a tendency (P = 0.15) for an IGF-I selection line x sex interaction for RFI. Bulls from the low IGF-I selection line had numerically lesser RFI than those from the high IGF-I selection line, whereas in heifers, the IGF-I selection line had no effect on RFI. In studies 1 and 2, weaning and initial IGF-I concentrations were not correlated with either feed conversion ratio or RFI. However, regression analysis revealed a sex x IGF-I concentration interaction for initial IGF-I concentration in study 1 and weaning IGF-I concentration in study 2 such that the regression coefficient was positive for bulls and negative for heifers. These data suggest that genetic selection for postweaning serum IGF-I concentration had a minimal effect on RFI in beef cattle.     

Growth performance and plasma insulin-like growth factor I concentrations in sheep selected for high weaning weight

A study was undertaken to determine the effect of selection for high weaning weight on concentrations of plasma insulin-like growth factor I (IGF-I) in sheep and to evaluate the usefulness of measuring IGF-I as an aid in identification of genotypes with a higher growth potential. Lambs from two lines selected for high 120-d weight (HW and DH) and an unselected control (C) were weighed and blood samples collected monthly from birth to weaning (4 mo. of age). A clear differentiation in size occurred after 1 mo of age between lines, between sexes, and between singles and twins. At weaning, selected lines were 3.8 and 5.0 kg heavier than controls. Plasma IGF-I concentrations were 1.5 to 2 times higher (P less than .001) in males than in females after 1 mo of age. There were no significant differences in IGF-I concentration between lines or types of birth. However, line DH and single lambs on average had higher concentrations of IGF-I. Within sex and type of birth correlations between IGF-I concentrations at 0, 1, 2, 3, and 4 mo and 4-mo BW ranged from -.16 to .49 in the three lines, and most were not significant. Coefficients of variation for IGF-I concentrations (36 to 50%) were two to three times higher than those for BW (11 to 15%). Due to the high variability of IGF-I measurements, the low correlations between IGF-I concentration and BW, and the small differences in IGF-I between control and selected lines, measurement of plasma IGF-I is unlikely to be an effective aid to selection for growth rate in sheep.     

Genetic parameter estimates for serum insulin-like growth factor-I concentration and ultrasound measurements of backfat thickness and longissimus muscle area in Angus beef cattle

A divergent selection experiment for serum IGF-I concentration began at the Eastern Ohio Resource Development Center in 1989 using 100 spring-calving (50 high line and 50 low line) and 100 fall-calving (50 high line and 50 low line) purebred Angus cows. Following weaning, bull and heifer calves were fed in drylot for a 140-d period. Real-time ultrasound measurements of backfat thickness and longissimus muscle area were taken on d 56 and 140 of the postweaning test. Only ultrasound data from calves born from fall 1995 through spring 1999 were included in the analysis. At the time of this study, IGF-I measurements were available for 1,521 bull and heifer calves, and ultrasound data were available for 636 bull and heifer calves. Data were analyzed by multiple-trait, derivative-free, restricted maximum likelihood methods. Estimates of direct heritability for IGF-I concentration at d 28, 42, and 56 of the postweaning period, and for mean IGF-I concentration were 0.26 +/- 0.07, 0.32 +/- 0.08, 0.26 +/- 0.07, and 0.32 +/- 0.08, respectively. Direct heritabilities for ultrasound estimates of backfat thickness ranged from 0.17 +/- 0.11 to 0.28 +/- 0.12, whereas direct heritabilities for longissimus muscle area ranged from 0.20 +/- 0.10 to 0.36 +/- 0.12, depending on the time of measurement and the covariate used for adjustment (age vs. weight). Direct genetic correlations of IGF-I concentrations with backfat thickness at d 56 and 140 and with longissiumus muscle area at d 56 and 140 averaged 0.02, 0.20, -0.08, and 0.23, respectively, when age was used as the covariate for both IGF-I and ultrasound measurements. Corresponding genetic correlations when age was used as the covariate for IGF-I and weight was used as the covariate for ultrasound measurements were 0.05, -0.07, -0.22, and -0.04, respectively. Therefore, the positive associations of serum IGF-I concentration with backfat thickness and longissimus muscle area at d 140 seem to have been partially mediated by weight. Results of this study do not indicate strong associations of serum IGF-I concentration with fat thickness or muscling of bulls and heifers during the postweaning feedlot period.     

Estimates of beef growth trait variances and heritabilities determined from field records

Variance components were estimated from field-collected performance records for use in national beef sire evaluation mixed-model programs. Estimates of residual error variances (sigma 2e), sire effect variances (sigma 2s) and dam effect variances (sigma 2d) were obtained for the American Hereford and the American Angus breeds for each of three growth traits: birth weight, weaning weight and postweaning gain. Estimates obtained for birth weight were sigma 2e, 8.43 and 9.26 kg2; sigma 2s, 1.34 and .66 kg2; and sigma 2d, 3.24 and 3.70 kg2 for the Hereford and Angus breeds, respectively. Estimates obtained for weaning weight were sigma 2e, 438.09 and 267.38 kg2; sigma 2s, 20.37 and 17.13 kg2; and sigma 2d, 162.25 and 157.28 kg2 for the Hereford and Angus breeds, respectively. Estimates obtained for postweaning gain were sigma 2e, 425.75 and 374.33 kg2; sigma 2s, 20.08 and 16.49 kg2; and sigma 2d, 41.74 and 48.61 kg2 for the Hereford and Angus breeds, respectively.     

Experimental selection for calving ease and postnatal growth in seven cattle populations. II. Phenotypic differences

Effects of selection for 2-yr-old heifer calving ease (reduced calving difficulty score) on phenotypic differences between select and control lines of cattle for birth, growth, yearling hip height, and pelvic measurements were estimated. The selection objective was to decrease calving difficulty score in 2-yr-old heifers, while either maintaining or increasing yearling weight. The control line objective was to maintain or increase yearling weight by the same amount as the select lines and to maintain or proportionally increase birth weight. Select and control lines were formed in 4 purebred and 3 composite populations. Selection began in 1992 and select (n = 6,926) and control (n = 2,043) line calves were born from 1993 through 1999. Selection was based on EBV calculated from a 4-trait BLUP with observations on 2-yr-old calving difficulty scores, birth weight, weaning weight, and postweaning gain. Calving difficulty was scored on a scale from 1 (unassisted) to 7 (caesarean). All birth traits in select lines differed significantly from control lines. Averaged over 7 yr, select lines calved 3.0 +/- 0.5 d earlier, had 1.8 +/- 0.5 d shorter gestations, were 2.99 +/- 0.32 kg lighter at birth, had 5.6 +/- 1.5% fewer calves assisted at birth (averaged across dam ages), and 2-yr-old heifers had 0.80 +/- 0.08 lower calving difficulty score. Select lines averaged 19.8% lower 2-yr-old heifer calving assistance, but there was no difference in calving assistance of older cows, resulting in a highly significant interaction of selection and dam classification. Preweaning ADG was increased 15 +/- 9 g/d (1.7%) in select lines. Increased preweaning gain offset decreased birth weights in select lines, resulting in weaning weights that did not differ (P = 0.71). Postweaning ADG (P = 0.16) and yearling weight (P = 0.41) also did not differ. Increased preweaning ADG in select lines was not maintained after weaning. Select line hip heights were 0.70 +/- 0.21 cm shorter when measured as yearlings. Pelvic height, width, and area of select heifers measured 25 to 74 d after yearling weights were not significantly different. The differences between select and control lines significantly changed over the course of the experiment for some traits. In the final 2 yr of the experiment, select lines had 3.9 kg lower birth weight and 1.3 cm shorter hip heights. Selection can be used effectively to reduce 2-yr-old calving difficulty and calving assistance while maintaining or increasing yearling weight.