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M R Dentine

Publications and source records attributed to M R Dentine.

At least 19 recordsLinked to original sources

Linkage disequilibrium and selection response in two-stage marker-assisted selection of dairy cattle over several generations.

A stochastic simulation was carried out to investigate the advantage of marker-assisted selection (MAS) in comparison with traditional selection over several generations. The selection goal was a sex-limited trait or a linear combination of traits with a polygenic component, two unlinked additive QTL and a non-genetic component. The simulated QTL were moderate or large and the allele frequencies were varied. Two stages of selection among the male offspring were carried out. In the first stage marker information was used to select among full sibs (MAS) or one full sib was chosen at random. In the second stage young bulls were selected based on a progeny test. The response in total genetic gain was faster with MAS than with traditional selection and persisted over several generations. With a QTL of moderate size and initial allele frequencies of the favourable allele of 0.05 the response with MAS was 6% higher than with traditional selection in the sires selected after progeny test. MAS in a within-family two-stage selection scheme improved the genetic merit of selected bulls even when linkage disequilibrium between QTL and polygenes was initially increased.

Animals↗

Evidence for quantitative trait loci affecting twinning rate in North American Holstein cattle.

Twinning in dairy cattle has been associated with many negative health and reproductive events that cause economic loss to the producer. Reports have suggested that twinning rates are increasing and that there may be a positive relationship between milk production and twinning frequency. Putative quantitative trait loci (QTL) for twinning and ovulation rate on bovine chromosomes 5, 7, 19 and 23 have been previously identified in other populations. The objective of this study was to detect and possibly confirm the existence and effects of these QTL in the North American Holstein population. Half-sib families of 20 North American Holstein sires with above average twinning rate predicted transmitting abilities (PTA) comprised the sample population under investigation. Twinning rate PTA values had been estimated from calving data. DNA extracted from semen samples was analysed using 45-61 microsatellite markers across the four chromosomes. Marker heterozygosity of the patriarchs averaged 62%. Evidence of twinning QTL was found in multiple families on chromosomes 5, 7 and 23 and in one family on chromosome 19. Four of the sires formed one three-generation family: one sire and three half-sib sons with sons of their own. This extended family was analysed with additional markers confirming a twinning QTL of significant size on chromosome 5.

Animals↗

Indirect prediction of herd life in Guernsey dairy cattle.

Production and type data were used to investigate the relationships of these traits with herd life data in US Guernsey cows that calved from 1985 through 1990. Two definitions of herd life were used: actual days from birth to disposal (true herd life) and herd life adjusted for milk production (functional herd life). Genetic parameters were calculated with data from cows that had an opportunity to reach 84 mo of age (n = 18,725). Linear type traits were preadjusted for stage of lactation and age at classification. True herd life was preadjusted for age at first calving and for functional herd life, within herd-year quartile ranking for milk yield. The (co)variance components for true and functional herd life, milk, fat, protein, and 15 linear type traits were estimated with multiple-trait REML in an animal model. Heritability estimates for true and functional herd life were 0.12 for both traits. Estimated genetic correlations of herd life with body size traits were from -0.14 to -0.29, with feet and leg traits were from -0.10 to 0.06, and with udder traits were from -0.09 to 0.24. These correlation parameters were used for indirect prediction of herd life from available production and type information in Guernseys.

Aging↗

Twinning rates for North American Holstein sires.

Calving data of North American Holsteins were analyzed using a linear sire model and a threshold sire model to estimate fixed effects and sire predicted transmitting abilities (PTA) for twinning rate. The data were 1,324,678 births of 37,174 sires of cows from the National Association of Animal Breeders (NAAB) calving ease database. All twins were assumed to be dizygotic. Triplets were not included in the analysis. The twinning rate was 5.02%. The sire model included relationships among sires and fixed effects of herd-years, season, parity, and sire groups. Different estimates of heritability due to models and restrictions on data have been demonstrated. Heritability estimates for the sire of the cow effect were 2.10% by the linear model analysis and 8.71% by the threshold model analysis. Sire PTA for twinning rate ranged from 1.6 to 8.0%. Mean incidence of twins increased from first to fifth and later parities: 1.63, 5.22, 6.66, 7.19, and 7.19%, respectively. Some changes with season were also evident. The incidence of twins was highest in April to June, at 5.88%, and lowest in October to December, at 4.23%. Sire group effects showed that sires born after 1990 had a higher incidence of twins than sires born before 1990. The mean twinning rate for sires born before 1980 was 4.55% compared with a mean of 5.58% for sires born after 1991. Characteristics of individual sire evaluations are discussed. Ample opportunity exists to change the incidence of twins in the Holstein population. Sire selection can be used to reduce the incidence of twins and also the increased cost of production associated with twins. From a national perspective, a reduction in the incidence of twin births can result in a saving of as much as $55 million per year.

Animals↗

Development of an efficient method to produce uniformly haploid parthenogenones.

Bovine ovaries (paired by cow) were obtained from a local abattoir and cumulus oocyte complexes were aspirated within six hours of slaughter. Two methods for activation [(1) calcium ionophore (ionomycin) alone (n = 191); and (2) ionomycin followed by the protein synthesis inhibitor cycloheximide (n = 207)] were evaluated for production of bovine parthenogenones. Activation with ionomycin alone resulted in a development rate of 33%, while activation with ionomycin and cycloheximide sequentially resulted in a development rate to two-cell stage of 49%. A procedure was developed to expedite accurate evaluation of activated oocytes for uniformly haploid development. Uniformly haploid parthenogenones that cleaved at least once in four days of in vitro culture were individually prepared for genetic analysis. Three techniques: (1) phosphate buffered saline; (2) TL-HEPES with 0.2% ovine serum albumin; and (3) TL-HEPES with 0.2% polyvinyl pyrrolidone were compared to harvest parthenogenones for genetic analysis. The only effective method that did not create spurious results during later genetic analysis was TL-HEPES with 0.2% polyvinyl pyrrolidone. Based on the results of this study, we estimate that an average of 5-7 uniformly haploid bovine parthenogenones can be realized from each donor (using pairs of ovaries). These parthenogenones, when maintained as family units, will be valuable for accomplishment of female-specific genetic linkage analysis.

Animals↗

Random amplified polymorphic DNA markers in crosses between inbred lines of Rhode Island red and White Leghorn chickens.

Reciprocal crosses and backcrosses were conducted between inbred Rhode Island Red and White Leghorn chickens differentiated for egg production and egg quality traits. Random amplified polymorphic DNA (RAPD) markers distinguishing inbred lines were detected. Twenty-two polymorphic bands were found from screening 120 single 10-mer random primers of which two were consistent with sex-linked markers. Of 90 pairwise two-point linkage analyses completed for the autosomal markers, four close linkages (8.2 cM to 14.9 cM) were significantly different from zero.

Animals↗

Development of bovine microsatellite markers from a microsatellite-enriched library.

A bovine genomic library enriched for DNA fragments bearing poly(dC-dA).poly(dG-dT) sequences was prepared and screened. Twenty-four clones bearing microsatellites were subject to sequence analysis and marker development as appropriate. Three of the 24 clones had microsatellites that were not evaluated for marker development owing to presence of a satellite element in two cases and limited repeat length in the third. Of the remaining 21 clones, all but one yielded polymorphic microsatellites. All but two of the polymorphic markers could be assigned to chromosomal locations by either linkage analysis or on the basis of X-linked inheritance as determined by heterozygosity limited to females. An unexpected clustering of markers was observed as 4 of the 20 polymorphic microsatellites mapped to a region of less than approximately 30 cM on Chromosome (Chr) 19, and four markers displayed X-linked inheritance.

Animals↗

Modulation of bovine oocyte-cumulus cell complex maturation and fertilization in vitro by glycosaminoglycans.

Oocyte-cumulus cell complex maturation and fertilization potential of 4700 bovine oocytes in the presence of various intrafollicular regulators were studied. Endpoints for oocyte maturation included cumulus cell expansion, retention of [3H]hyaluronic acid, elevated cyclic AMP concentrations, and germinal vesicle breakdown. Media supplemented with FSH and fetal bovine serum stimulated oocyte maturation and fertilization. Heparin and mixed glycosaminoglycans (40% heparan sulfate and 60% dermatan sulfate) stimulated cumulus cell expansion and increased [3H]hyaluronic acid but decreased cyclic AMP and reduced percentages of oocytes with germinal vesicle breakdown at 12 h. Oocytes cultured in heparin or mixed glycosaminoglycans were incapable of fertilization. Addition of serum to oocytes treated with heparin decreased cumulus cell expansion. Addition of FSH to heparin and serum cultures did not overcome the inhibitory effect of serum on heparin-induced expansion. Dermatan sulfate failed to stimulate expansion of cumuli but resulted in cells retaining [3H]hyaluronic acid and elevated cyclic AMP content of oocytes. Dermatan sulfate did not affect the percentage of germinal vesicle breakdown at 12 h. Nitrogen-desulfated heparin did not promote any signs of oocyte maturation. These results demonstrate that heparin and mixed glycosaminoglycans stimulate events related to oocyte maturation but were not capable of preparing oocytes for fertilization. The addition of serum or desulfation of heparin inhibited heparin effects on oocyte maturation.

Animals↗

Chromosome substitution effects associated with kappa-casein and beta-lactoglobulin in Holstein cattle.

Allelic variants of kappa-casein and beta-lactoglobulin were used to estimate chromosome substitution effects on transmitting abilities for yield traits among sons of two Holstein sires. Sire 1 was a heterozygote for both loci, whereas sire 2 was a heterozygote for beta-lactoglobulin only. Transmitting abilities for fat percentage and the exchange of protein and fat (protein yield minus fat yield) were influenced by kappa-casein genotype among offspring of sire 1. The B allele of kappa-casein was associated with a decrease in fat percentage, whereas fat yield was not affected; the result was 4.5 kg more transmitting ability for protein than for fat. Favorable chromosome substitution effects on transmitting abilities for fat percentage, protein yield, and the exchange of protein and fat were also observed for the A allele of beta-lactoglobulin among offspring of sire 1; there were consistent but not significant estimates for sire 2. These results suggest that different estimates could be obtained from offspring of different parents, perhaps from linkage disequilibrium between families. The chromosome substitution effects appeared to be in the direction opposite to the average correlation of milk fat and protein content; marker-assisted selection for increased yield of protein would result in decreased fat yield.

Alleles↗

Inheritance of tinted eggshell colors in white-shell stocks.

The present study was conducted to study the genetics of tinted eggshell colors in two breeds of chickens laying white-shell eggs. Reciprocal crosses were made between an inbred White Leghorn line (ES) and an inbred Ancona line (ANC). The F1 birds were intercrossed and F1 females were backcrossed to each of the original lines. Eggshell color from each resultant group was measured using a Minolta chromometer, and a value (e) representing the color intensity adjusted by hue and saturation was used as the measurement criterion. Age, hatch group, and crosses each contributed significantly to the variation seen in eggshell color. Distribution comparisons indicated that two major autosomal loci affected the trait in these lines: one gene having incomplete dominance controls the amount of pigment deposition; the second completely inhibits pigment deposition when homozygous recessive. A test of goodness of fit supported this hypothesis. Genetic components were estimated by linear models. Epistasis, dominance, and additive effects contributed significantly to this trait. No sex-linked effects were noted.

Analysis of Variance↗

The response of lactating dairy cows to increasing levels of whole roasted soybeans.

Twenty-four Holstein cows, including four primiparous and four ruminally cannulated, were in replicated 4 x 4 Latin squares with 21-d periods to determine the effects of feeding level of whole roasted soybeans on lactation performance and rumen function. Cows were fed rations containing a 50:50 forage:concentrate ratio with 0, 12, 18, or 24% of diet DM as whole roasted soybeans. Rations contained 16.8, 16.9, 18.6, and 19.7% CP and 1.68, 1.71, 1.72, and 1.74 Mcal NEL/kg DM, respectively. Milk production and milk fat percentages for diets containing 0, 12, 18, or 24% whole roasted soybeans were 34.9, 37.5, 38.5, and 38.8 kg/d and 3.23, 3.20, 3.32, and 3.37%, respectively. Milk protein percentage was depressed at all levels of whole roasted soybeans. Ruminal pH, VFA molar percentages except valerate, and DM disappearance of forage from dacron bags did not differ among treatments. Responses were similar among primiparous and multiparous cows. Results suggest benefit from feeding whole roasted soybeans at levels up to 18% of ration DM without adversely affecting DMI, milk fat, or rumen fermentation.

Animals↗