In six patients with acanthosis nigricans variable degrees of glucose intolerance, hyperinsulinemia and marked resistance to exogenous insulin were found. Studies of insulin receptors on circulating monocytes suggest that the insulin resistance in these patients was due to a marked decrease in insulin binding to its membrane receptors. When these patients were fasted, there was a fall in plasma insulin but no increase in insulin binding, suggesting that the receptor defect was not secondary to the hyperinsulinemia. The clinical features shared by these cases and several similar ones previously reported may be divided into two unique clinical syndromes: Type A, a syndrome in younger females with signs of virilization or accelerated growth, in whom the receptor defect may be primary, and Type B, a syndrome in older females with signs of an immunologic disease, in whom circulating antibodies to the insulin receptor are found.

Records on 1,180 young Angus bulls and heifers involved in performance tests were used to estimate genetic and phenotypic parameters for feed intake, feed efficiency, and other postweaning traits. The mean age was 268 d at the start of the performance test, which comprised 21-d adjustment and 70-d test periods. Traits studied included 200-d weight, 400-d weight, scrotal circumference, ultrasonic measurements of rib and rump fat depths and longissimus muscle area, ADG, metabolic weight, daily feed intake, feed conversion ratio, and residual feed intake. For all traits except the last five, additional data from the Angus Society ofAustralia pedigree and performance database were included, which increased the number of animals to 27,229. Genetic (co)variances were estimated by REML using animal models. Direct heritability estimates for 200-d weight, 400-d weight, rib fat depth, ADG, feed conversion,and residual feed intake were 0.17 +/- 0.03, 0.27 +/- 0.03, 0.35 +/- 0.04, 0.28 +/- 0.04, 0.29 +/- 0.04, and 0.39 +/- 0.03, respectively. Feed conversion ratio was genetically (r(g) = 0.66 ) and phenotypically (r(p) = 0.53) correlated with residual feed intake. Feed conversion ratio was correlated (r(g) = -0.62, r(p) = -0.74) with ADG, whereas residual feed intake was not (rg = -0.04, r(p) = -0.06). Genetically, both residual feed intake and feed conversion ratio were negatively correlated with direct effects of 200-d weight (r(g) = -0.45 and -0.21) and 400-d weight (r(g) = -0.26 and -0.09). The correlations between the remaining traits and the feed efficiency traits were near zero, except between feed intake and feed conversion ratio (r(g) = 0.31, r(p) = 0.23), feed intake and residual feed intake (r(g) = 0.69, r(p) = 0.72), and rib fat depth and residual feed intake (r(g) = 0.17, r(p) = 0.14). These results indicate that genetic improvement in feed efficiency can be achieved through selection and, in general, correlated responses in growth and the other postweaning traits will be minimal.

Evidence for genetic variation in feed efficiency of beef cattle is reviewed in this paper, and ways in which this variation might be used in selection programs to improve beef cattle in Australia are discussed. Efficiency of beef production systems is determined by feed and other inputs of all classes of animals in the production system as well as outputs in terms of slaughter progeny and cull cows. Different indices have been used to express aspects of efficiency on cattle over certain periods of the production cycle. Use of these indices is discussed, and then evidence for genetic variation in both growing animals and mature animals is reviewed. Genetic variation in feed efficiency exists in both growing and mature cattle, although information is lacking to determine whether variation in total production system efficiency exists. The physiological basis for observed variation in feed efficiency is discussed, with differences in requirements for maintenance, body composition, proportions of visceral organs, level of physical activity, and digestion efficiency identified as possible sources of variation. Selection to improve efficiency might be achieved by measuring feed intake of growing animals and utilising genetic correlations that are likely to exist between efficiency of growing animals and mature animals. Measurement of feed intake might occur in central test stations, or methods may be developed to measure feed intake on-farm. Ways of utilising information generated in genetic evaluations are discussed, and it is concluded that estimated breeding values for feed intake after a phenotypic adjustment for growth performance would be most practical, although not theoretically optimal. Such estimated breeding values would best be used in an economic selection index to account for genetic correlations with other traits, including feed intake of the breeding herd, and the economic value of feed in relation to other traits. Future research should be directed towards understanding the genetic relationships between feed intake and other traits in the breeding objective, and to find ways to reduce the cost of measurement of feed intake, including a search for genetic markers.