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Biomedical subjects

M Soller

Publications and source records attributed to M Soller.

At least 91 records · Page 5Linked to original sources
PubMed1987

Restriction fragment length polymorphisms in dairy and beef cattle at the growth hormone and prolactin loci.

Two bovine populations, a Holstein-Friesian dairy stock and a synthetic (Baladi X Hereford X Simmental X Charolais) beef stock, were screened for restriction fragment length polymorphisms (RFLPs) at the growth hormone and prolactin genes. Most RFLPs at the growth hormone gene are apparently the consequence of an insertion/deletion event which was localized to a region downstream of the structural gene. The restriction map for the genomic region including the growth hormone gene was extended. Two HindIII RFLPs at the growth hormone locus, as well as several RFLPs at the prolactin gene, seemed to be the consequence of a series of point mutations. The results are discussed in terms of the possibility that minor genomic variability underlies quantitative genetic variation.

Animals↗
PubMed1986

Restriction fragment length polymorphism among Israeli Holstein-Friesian dairy bulls.

Israeli Holstein-Friesian dairy bulls were screened for restriction fragment length polymorphisms by hybridizing cloned DNA probes for bovine growth hormone, for chymosin, and for rat muscle beta-actin to restriction endonuclease-digested DNA immobilized on nitrocellulose filters. The population proved to be polymorphic at the growth hormone locus, with evidence consistent with the phenotypes being inherited in allelic fashion. A low level of polymorphism was also observed at one of the beta-actin gene family loci. The chymosin locus was monomorphic with the restriction enzymes utilized. The results illustrate the power of restriction fragment length polymorphism methodology in visualizing genetic variability in dairy cattle populations.

Actins↗
PubMed1984

Effect of diet and early quantitative feed restriction on the minimum weight requirement for onset of sexual maturity in white rock broiler breeders.

The effect of diet and feed restriction on minimum weight for onset of sexual maturity was studied in White Rock broiler breeders. In the restriction experiment, three groups of birds were subjected to moderate, severe, and very severe quantitative food restriction during the rearing period (19 week target weights: 1900, 1300, and 700 g, respectively). From 20 to 24 weeks body weight was equalized at 2200 g, and from 24 weeks birds were allowed to gain about 150 g/week until first egg. In the diet experiment, two groups of birds were raised under severe quantitative food restriction during the rearing period and then allowed to gain about 150 g/week on a low metabolizable energy/protein (ME/P) ratio diet (25.4% protein, ME/P = 116) and on a high ME/P ratio (14.7% protein, ME/P = 219) until first egg. All birds were killed at first egg. Birds of the three restriction groups entered lay at the same lean body weight and ash and protein content, but at different age, carcass weight, shank length, dry matter, and fat content. Birds of the two diet groups entered lay at the same lean body weight, shank length, and ash content but at different carcass weight, dry matter, and fat content. Considering both experiments together, birds of the different treatment groups entered lay at similar lean body weight and ash content but differed in age, carcass weight, shank length, dry matter, and fat content.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗
PubMed1984

Minimum weight for onset of sexual maturity in female chickens: heritability and phenotypic and genetic correlations with early growth rate.

The heritability of minimum weight for onset of sexual maturity in chickens (WTSXM) and its phenotypic and genetic correlations with early growth rate were studied in a Leghorn (L) layer stock, in two White Rock (WR) broiler stocks, and in the F4, F5, and F6 segregating generations of a White Rock X Leghorn (WR X L) cross. Mean heritability of WTSXM was .38 in the WR populations and .84 in the WR X L cross populations. Mean WTSXM of the various genetic stocks were closely related to their mean early growth rate. The mean phenotypic correlation of WTSXM and early growth rate was .07 in the WR populations but .47 in the WR X L cross populations. Estimates of the genetic correlation of WTSXM with early growth rate were high, and uniform in sign in the WR X L cross populations but smaller in magnitude and variable in sign in the WR populations. The implications of these results with respect to WTSXM as a breeding objective are discussed.

Animals↗
PubMed1981

Extracellular protein release and its response to pH level in Saccharomyces cerevisiae.

Saccharomyces cerevisiae grown in batch culture at pH 5.5 releases 0.1 to 0.2 pg protein per cell to the external medium over a period of four to five days, final concentration 20-40 micrograms/ml. Cells grown at pH 3.0 release 10-fold this quantity (1-2 pg/cell, final concentration 100-200 micrograms/ml). A kinetic model based on published behavior of periplasmic protein gave a good fit to the observed kinetics of exoprotein yield. The electrophoretic pattern of exoprotein differed from that of cell lysate protein, and exoprotein synthesis was apparently limited to early stages of the life cycle. These results are consistent with the identification of exoprotein as periplasmic protein released to the external medium through the cell wall. Analysis of the observed kinetics of exoprotein yield, utilizing the kinetic model suggests that the greater exoprotein production of cells grown at pH 3.0 was due entirely to greater synthesis of periplasmic proteins while the fraction of periplasmic protein released per unit time was greater for cells grown at pH 5.5. The latter conclusion is supported by thicker cell walls of cells grown at pH 3.0 as observed by electron microscopy. At an applied level the apparent limitation of exoprotein synthesis to the first few hours of cell life, the slow leakage of exoprotein through the cell wall, and the dilute nature of a yeast suspension do not favor the utilization of yeast cells for direct conversion of substrate into protein released to the external medium.

Cell Wall↗
PubMed1981

Immune response to Newcastle disease virus vaccine, fowl-pox vaccine, and Escherichia coli vaccine in Bedouin and White Leghorn chickens.

Immune response to Newcastle disease virus (NDV) vaccine, fowl pox, and E. coli vaccine was compared in the native Bedouin fowl of the Sinai desert, in a commercial Leghorn layer strain, and in the reciprocal crosses between them. Differences were not found in antibody titer levels to attenuated or inactivated NDV vaccines, in the proportion of birds showing post-vaccination immunity to fowl pox, or in the kinetics of postvaccination NDV titer levels. Rate of development of titer to Escherichia coli from day 1 to day 4, however, was significantly more rapid in Bedouin chicks than in the purebred Leghorn or the reciprocal crosses.

Animals↗
PubMed1981

Genetic and phenotypic correlations between immune response to Escherichia coli and to Newcastle disease virus vaccines.

Genetic and phenotypic variation and covariation in immune response to inactivated Newcastle disease virus (NDV) vaccine and to Escherichia coli vaccine were studied in commercial poultry strains. Within any given experiment there was no tendency for individual birds to respond in a correlated manner to NDV and E. coli vaccines. There were highly significant differences between sire families in immune response to NDV vaccine (57 sire families) and to E. coli vaccine (35 sire families). Heritabilities of immune response levels to NDV and to E. coli were .41 and .25, respectively. In both cases, additive genetic standard deviations were slightly over 1.0 titer unit. The correlation between sire-family means for response to NDV and sire-family means for response to E. coli (35 sire families) was .077 and statistically nonsignificant. Thus, the data provide evidence for the presence of significant genetic variation in immune response with respect to two endemic disease antigens, but they provide no evidence for a genetic correlation in response to the two antigens.

Animals↗
PubMed1980

Compensatory growth and sexual maturity in broiler females reared under severe food restriction from day of hatching.

1. Compensatory growth and the onset of lay were studied in White Rock broiler females severely restricted in food intake from day of hatching. 2. When changed to feeding ad libitum the restricted birds gained weight rapidly, but stabilised at a mean body weight 500 to 700 g less than that of controls fed ad libitum. Egg production was similar to that of controls. 3. Birds maintained at low mean body weight ( 2 224 g at 42 weeks) by continued restriction did not come into lay. In groups maintained at somewhat higher mean body weights (2 300 to 2 700 g) for period of up to a year, some birds came into lay. 4. Birds fed ad libitum showed accelerated development of comb, ovary and oviduct and weighed 2 300 to 2 700 g between 14 and 15 weeks of age, but did not come into lay until 20.5 weeks of age. 5. These results suggest that a minimum body weight and age may be required for the onset of lay in this strain.

Animals↗
PubMed1976

Genetic and environmental correlations between brain weight and maze learning in inbred strains of mice and their F1 hybrids.

The relationships among body weight, cerebellum weight, cerebrum weight, maze-learning ability in a double T-maze, and discrimination learning in a Y-maze were studied in six inbred strains of mice and some of their F1 hybrids. The subjects were 131 male albino mice from 14 genotypic groups: five inbred groups and nine groups of crossbred offspring. Intra- and intergroup correlations were computed between all possible pairs of the anatomical and behavioral traits. A significant difference between the intragroup and intergroup correlations for any pair of variables was taken to indicate the presence of a genetic correlation between the two variables. On this basis, positive genetic correlations were indicated between T-maze learning ability and Y-maze learning ability, between body weight and T-maze learning ability, and possibility between body weight and both cerebellum and cerebrum weight and between cerebrum weight and T-maze learning ability. Negative genetic correlations were indicated between cerebellum weight and running time in both mazes and between total number of successes in the Y-maze and Y-maze running time.

Animals↗