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Biomedical subjects

K E Nestor

Publications and source records attributed to K E Nestor.

At least 19 recordsLinked to original sources

Inheritance of breast muscle morphology in a line of turkeys selected for increased egg production, its randombred control line, and reciprocal crosses between them.

Breast muscle morphology was studied at 16 wk of age in a line (E) selected over 45 generations for increased egg production, its randombred control line (RBC1), and reciprocal crosses between the E and RBC1 lines. A sample of 10 birds per genetic group-sex subgroup was killed with restraint to prevent flapping of the wings. The skin was removed from the breast region and a sample of breast muscle was obtained in a manner to prevent contraction. The muscle samples were dehydrated, cleared, embedded in paraffin, sectioned, incubated, and rehydrated before staining with hematoxylin and eosin. Four sections from the same muscle from each bird were placed on a slide and the slides were viewed for muscle morphology characteristics with a microscope and digitally recorded. Five fields of each section were viewed. Representative sections of each bird were given a score by 4 individuals based on breast muscle morphology. The scores ranged from 1 (little extracellular matrix and indistinct muscle fibers) to 5 (large extracellular space and distinct muscle fibers). Scores from 2 to 4 were intermediate to these extremes. The data were analyzed for sexes separate and combined. The E line had lower breast muscle morphology scores than the RBC1 line for males and sexes combined, indicating additive genetic variation in the scores. Nonadditive genetic variation was not an important source of variation for breast muscle morphology scores based on the contrast of the average of the parental lines with the average of the reciprocal crosses for males, females, or sexes combined. In 5 of 6 possible comparisons, the breast muscle morphology scores of the reciprocal cross were not significantly different from the line of the dam in the reciprocal cross. The only exception was for the E sire x RBC1 dam cross based on the data for females, wherein the breast muscle morphology scores were higher in the cross than in the pure RBC1 line. The results of the current study confirm the maternal inheritance of breast muscle morphology scores at 16 wk of age that has been previously reported.

Animals↗

Differential expression of membrane-associated heparan sulfate proteoglycans in the skeletal muscle of turkeys with different growth rates.

Heparan sulfate proteoglycans (HSPG) are key components of the cell membrane and extracellular matrix of skeletal muscle cells. Two major groups of membrane-associated HSPG found in skeletal muscle are syndecans (SYN) and glypicans (GPC), both of which can regulate growth factor activities and, thus, modulate cell proliferation and differentiation. In the current study, the mRNA expression of a group of membrane-associated HSPG (SYN 2 through 4 and GPC 1) was investigated in embryonic pectoralis major muscle [embryonic days (ED) 14, 16, 18, 20, 22, 24] and myogenic satellite cells isolated from males of a turkey genetic line selected for increased 16-wk BW (F line) and an unselected randombred control (RBC2 line) from which the F line was developed. The mRNA expression was measured by a real-time quantitative PCR approach. The SYN 2 and SYN 4 expression exhibited a similar pattern during embryonic p. major muscle development, which remained constant from ED 14 to ED 22 and declined sharply from ED 22 to ED 24 to a very low level. In contrast, the SYN 3 and GPC 1 expression showed a continuous decline from ED 14 to ED 24. The F line had higher SYN 2 (ED 14, 18, 20, 22), SYN 3 (ED 22), and SYN 4 (ED 22) expression than the RBC2 line. In myogenic satellite cells, initiating differentiation resulted in a decrease in SYN 2 expression and an increase in GPC 1 expression. Both SYN 3 and SYN 4 expression stayed almost constant through both the proliferation and differentiation stages. The proliferating satellite cells from the F line displayed higher SYN 4 expression than those from the RBC2 line. Collectively, the results from the current study suggest that membrane-associated HSPG are differentially expressed in both embryonic p. major muscle tissue and satellite cells isolated from F-line and RBC2-line male turkeys, implying their distinct roles in myogenesis and differing influence on muscle growth properties.

Aging↗

Genetics of growth and reproduction in the turkey. 16. Effect of repeated backcrossing of an egg line to a commercial sire line.

The turkey industry's view of the relative economic importance of growth and egg production has changed rapidly, and genetic changes by selection within lines may not be rapid enough to meet the changing needs. The objective of the present study was to determine the feasibility of rapidly increasing the BW of dam lines by repeated backcrossing of a dam line (E) to a commercial sire line (B). The experimental E line was selected long-term for increased egg production and was used as the model for a turkey dam line. The B line was larger (more than 3-fold) in BW at 8, 16, and 20 wk of age, had wider breasts (approximately 1.8-fold) at 16 wk of age, and had lower egg production for 180 d (about 3-fold) than the E line. Based on additive genetic variation, males in the F1 generation of the B x E cross did not differ from expected in BW at any age, but females of this cross had BW less than expected at 16 and 20 wk of age. In the F1 generation, breast width of the cross did not differ from the expected value, but egg production for 180 d was greater than expected (126.6 vs.102.3 eggs/hen). After 3 generations of backcrossing, the backcrosses exhibited a gain in 20-wk BW of 12.5 and 8.8 kg, respectively, for males and females; a gain of 5.9 and 5.3 cm in breast width at 16 wk of age for males and females, respectively; and a loss of 74.1 eggs per hen over a 180-d production period. Based on the results of the current and a previous study, limited backcrossing of a dam line to a sire line may be an economically feasible method to greatly increase the BW of dam lines without unduly sacrificing egg production. For maximum gains per generation, backcrossing probably should be used for a maximum of 2 or 3 generations.

Animals↗

Genetic variation in pure lines and crosses of large-bodied turkeys. 4. Body shape and carcass traits.

An experimental line (F) of turkeys selected long-term for increased 16-wk BW was reciprocally crossed with a primary breeding sire line (C) from a major international turkey breeder to study the inheritance of carcass traits and body shape. The birds were weighed and killed at 16 wk of age, and various measurements of muscling, leg bones, and body shape were made. The BW of males were 16.0 and 15.1 kg, respectively, in the C and F lines. The respective BW for females were 12.2 and 11.2 kg. Additive genetic variation, as indicated by differences between the F and C line, was a more important source of variation for measurements of muscling than for measurements of leg bones. The anterior and posterior depth of the body and the ratio of these measurements differed between the F and C lines. Body cavity volume index (length x width x height) differed between lines in females and sexes combined. The weights of some internal organs (gizzard, heart, liver, pancreas, and spleen), but not others (proventriculus and lungs), differed between lines, and the total weight of these organs was greater in the C line than in the F line. However, the ratio of total demand organs (muscles and bones) to the total weight of the supply organs was less in the F line than in the C line. Heterosis was a more important source of variation in body weight and weights of the pectoralis major and pectoralis minor muscle weights in males than in females. Heterosis for some body shape measurements (keel length, body depth 1, body depth 2, body depth ratio, body cavity height, and body cavity volume index) was significant in some comparisons. Heterosis (range = 3.64 to 3.99%) for leg muscle measurements (thigh muscles, drumstick muscles, and total leg muscles) was highly significant (P < or = 0.01) based on the analysis for both sexes. Differences between the reciprocal crosses of the F and C lines were more frequent in the present study than in previous studies in which the F line was reciprocally crossed with sire lines from 2 other commercial breeders. However, when the data from the previous studies and the current study were summarized, it appeared that the only reciprocal effect that was consistent was for the weight of the drumstick muscles, indicating sex linkage or maternal effects may influence the weight of these muscles.

Animals↗

Stress response differences and disease susceptibility reflected by heterophil to lymphocyte ratio in turkeys selected for increased body weight.

Three genetic lines of turkeys were compared for their responses to Escherichia coli challenge following dexamethasone injection (Dex) or E. coli challenge preceding transport stress (TS). The turkey lines were a slow growing line selected for increased egg production (Egg line), a fast growing line selected for increased 16-wk BW (F line), and a commercial line (Comm line). At 14 wk of age, the Dex group was treated with 3 injections of 2 mg of Dex/kg of BW followed by airsac challenge with 100 cfu of E. coli. The TS group was given the same E. coli challenge at 1 x 10(4) cfu/bird without Dex treatment, and was subjected to transport stress, including 12 h of holding time in a transport vehicle, 8 d after the challenge. All treated birds and untreated control birds were bled at the same time, which was 1 d after transport and 9 d after challenge with E. coli. The main effect mean (MEM) total leukocyte counts (WBC) and the percentages of eosinophils (Eos) and basophils (Baso) were the same for all 3 lines; however, the MEM percentages of heterophils (Het) and monocytes (Mono) and the heterophil/lymphocyte ratio (H/L) were lower and the percentage of lymphocytes (Lym) was higher in the Egg line compared with the 2 fast-growing lines. Both stress treatments increased WBC, Het, and H/L and decreased Lym in all 3 lines; however, these effects were significantly greater in both fast growing lines compared with the Egg line. Sixteen-week BW was unaffected by either treatment in the Egg line and was decreased by both treatments in the Comm line and by the Dex treatment in the F line. Main effect mean airsacculitis score (AS) was not affected by line and was significantly increased by TS and Dex treatments. Neither treatment affected AS of the Egg line birds, whereas Dex treatment increased AS of the F line, and both Dex and TS increased AS of the Comm line. Mortality was significantly higher in the Comm line compared with the Egg line and was intermediate in the F line. The differences between these lines in their disease resistance and physiological response to stress in 2 stress models suggests that increasing selection for BW of turkeys is accompanied by changes in the stress response resulting in increased susceptibility to opportunistic bacterial infection.

Animals↗

Genetic variation in pure lines and crosses of large-bodied turkey lines. 3. Growth-related measurements on live birds.

An experimental line (F) selected over 34 generations for increased 16-wk BW was reciprocally crossed with a primary breeding sire line (C) from a large international turkey breeder to study the inheritance of growth-related traits measured on live birds. All genetic groups were grown intermingled in confinement with sexes reared in different houses. The traits measured included BW at 8, 16, and 20 wk of age and shank length, shank width, shank depth, breast width, and walking ability scores at 16 wk of age. Walking ability was rated from 1 to 5 with 1 representing birds with no leg defects and no difficulty walking and 5 indicating birds with extreme lateral deviations of the legs and great difficulty walking. Ratings of 2, 3, and 4 represented intermediate values. The F line had a different growth pattern than the C line with the F line being larger than the C line at 8 wk of age, but the reverse was true at 16 and 20 wk of age. The difference in BW between the C and F lines increased from 16 to 20 wk of age. The C line had wider breasts than the F line at 16 wk of age. The F line had longer shanks than the C line. Shank width was larger in the C line than the F line for females but not males. No line difference in shank depth was observed. Walking ability scores at 16 wk of age were lower (better) in the C line than in the F line for males but not females. Significant heterosis in BW of the crosses of the F and C lines was observed at all ages in males (range = 3.3 to 5.6%) and only at 8 wk of age in females (3.6%). These results were similar to an earlier study in which the F line was crossed with a primary-breeding sire line from 2 other international turkey breeders. No significant heterosis in the crosses of the C and F line was observed for breast width and shank measurements. Heterosis was significant for walking ability scores of females (-3.0%) but not males. Reciprocal effects, a measure of sex linkage and maternal influences, were noted only for shank length and the direction of the difference was not the same in the 2 sexes.

Animals↗

Effect of genetic increases in egg production, age, and sex on muscle development in turkeys.

Breast muscle morphology was studied at 8 and 16 wk of age in a line (E) selected over 44 generations for increased egg production and its randombred control line (RBC1). A sample of 20 birds per sex-line-age subgroup was killed with restraint to prevent flapping of the wings. The skin was removed from the breast region, and a sample of breast muscle was obtained in a manner to prevent contraction. The muscle samples were dehydrated, cleared, embedded in paraffin, sectioned, and incubated and rehydrated prior to staining with hematoxylin and eosin. Four sections from the same muscle from each bird were placed on a slide, and the slides were viewed for muscle morphological characteristics with a microscope and digitally recorded. Five fields of each section were viewed. Representative sections for each bird were given a score by 4 individuals based on breast muscle morphology. The scores ranged from 1 (little extracellular matrix and indistinct muscle fibers) to 5 (large extracellular space and distinct muscle fibers). Scores from 2 to 4 were intermediate to these extremes. Breast muscle morphology scores did not differ between lines or ages but there was a significant interaction between lines and ages. The scores increased in the RBC1 line from 8 to 16 wk of age, but the reverse was true for the E line. Scores were higher in males than females. The results of the present study suggest that selection for increased egg production in dam lines should not greatly influence breast muscle morphology in commercial turkeys.

Aging↗

Genetic variation in body weight and egg production in an experimental line selected long term for increased egg production, a commercial dam line, and reciprocal crosses between lines.

A line (E) of turkeys selected long term (40 generations) for increased egg production was reciprocally crossed with a commercial dam line (BD). The BD line was larger and had better conformation than the E line, but the E line laid more eggs than the BD line. Heterosis was negative and significant for BW at 8, 16, and 20 wk of age (both sexes) and at 50% production (females only). Values for heterosis ranged from -3.1 to -5.5%. Negative heterosis was observed for breast width at 16 wk of age (10.8 and 3.0% for males and females, respectively). Positive heterosis values of 9.2, 10.2, and 11.3% were observed for egg production when based on 84, 120, and 180 d, respectively. Heterosis (-8.2%) was significant for rate of response to stimulatory lighting of 14 h light per day (days from stimulatory lighting to production of first egg). Based on data for a 180-d production period, heterosis was observed in average clutch length (12.6%) and rate of lay [number of eggs laid: (180 - total days broody)] (8.2%) but not in total days lost from broodiness or the effective length of the laying period (180 minus days lost in periods of 5 or more consecutive days at the end of the laying period). The present results along with those in the literature suggest that more heterosis in egg production traits might be expected in crosses of lines exhibiting extreme differences in BW and body conformation. The negative heterosis in BW in the BD and E reciprocal crosses reduces the commercial importance of such a cross to improve egg production.

Animals↗

Inheritance of breast muscle morphology in turkeys at sixteen weeks of age.

The inheritance of morphology of the pectoralis major muscle in turkeys at 16 wk of age was studied in a randombred control line (RBC2), a subline (F) of RBC2 selected long term for increased 16 wk BW only, and F1 and F2 crosses of the F and RBC2 lines. Samples of pectoralis major muscle were obtained from 10 males and 10 females of each genetic group in a manner to avoid muscle contraction. After being fixed and cross sectioned, the muscle samples were stained with hematoxylin and eosin to view muscle morphology. The stained sections were analyzed for muscle fiber width, number of fibers in a 136-microm2 area, and extracellular matrix perimysial (PW) and endomysial (EW) width in areas of sections in which accurate measurements could be made. Because muscle damage was evident in some sections and, therefore, morphological measurements might not have provided a complete overview of muscle morphology, sections of the F2 crosses were subjectively rated by 4 people. The ratings ranged from 1 (little extracellular matrix and indistinct muscle fibers) to 5 (large extracellular space and distinct muscle fibers). Ratings of 2 to 4 were intermediate to these extremes. Creatine kinase concentrations of blood samples taken immediately prior to collecting muscle tissue were obtained and correlated with muscle section ratings within genetic group and sex. The F and RBC2 lines differed in PW and EW but not in individual fiber measurements. In the F1 generation, heterosis was -10.4% (P < or = 0.01), 19.7% (P < or = 0.05), -25.2% (P < or = 0.01), and -34.3% (P < or = 0.01), respectively, for fiber width, number of muscle fibers, PW, and EW. The F2 crosses differed only in EW based on measurements of sections in which accurate measurements could be made. However, based on subjective ratings of the muscle sections, possible maternal inheritance was suggested, as the orthogonal contrast was significant (P < or = 0.01) for crosses with F dams as F1 parents vs. those with RBC2 dams as F1 parents, confirming a previous study. The correlation coefficient between creatine kinase concentration and muscle section ratings was -0.282 (P < or = 0.01) after adjustment for line and sex effects.

Aging↗

The influence of selection for increased body weight and sex on pectoralis major muscle weight during the embryonic and posthatch periods.

Skeletal muscle development and growth results from a complex series of highly organized processes. To address how myogenesis was influenced by selection for increased BW and by sex, both sexes from a turkey line (F) selected only for increased 16-wk BW and its genetic control line (RBC2) were used. Pectoralis major muscle was isolated and weighed from 15 individuals of each sex of the F and RBC2 lines at 14, 16, 18, 20, and 24 d of embryonic development and at 1, 8, 12, and 16 wk of age posthatch. The F line had significantly heavier p. major muscle weights than the RBC2 line beginning at 16 d of embryonic development, and the magnitude of the line differences generally increased with age through 16 wk posthatch The p. major muscle was consistently heavier in males than in females, but the differences between sexes were significant only at 16, 18, and 24 d of embryonic development and at 8 wk posthatch. There was no significant interaction between line and sex for weight of the p. major muscle at any age. The results indicated that selection for increased 16-wk BW in the F line altered growth of the p. major muscle by 16 d of embryonic development and changes were similar for both sexes.

Animals↗

Expression of fibroblast growth factor 2 and its receptor during skeletal muscle development from turkeys with different growth rates.

Fibroblast growth factor 2 (FGF2) is a key regulator of muscle cell proliferation and differentiation. To address how FGF2 and fibroblast growth factor receptor 1 (FGFR1) gene expression influences skeletal muscle development and growth, pectoralis major muscle was isolated at embryonic days (ED) 14, 16, 18, 20, 22, and 24, and at 1-, 8-, 12-, and 16-week posthatch from a turkey line (F) selected only for increased 16-week body weight and its genetic control line (RBC2). The mRNA levels of FGF2 and FGFR1 were measured by semi-quantitative reverse transcription polymerase chain reaction. Compared to the RBC2 line males, the F line males had higher FGF2 mRNA levels at ED 14 and 16, and higher FGFR1 mRNA levels at ED 18, but down-regulated FGF2 and FGFR1 gene expression at ED 22. Although no FGF2 mRNA was detected in posthatch muscle tissue, the F line turkeys had more FGFR1 gene expression at 8-, 12-, and 16-week posthatch than the RBC2 line turkeys. During myogenic satellite cell proliferation, the F line cells had higher FGF2 and FGFR1 mRNA levels than the RBC2 line cells. The satellite cell responsiveness to FGF2 treatment was evaluated by the ability of the cells to proliferate. The male satellite cells were more responsive to FGF2 stimulation than the female cells in both lines. These results suggest that the F line turkeys have increased FGF2 signaling that may affect muscle cell proliferation and differentiation, which may also lead to an enhancement in muscle development and growth rate.

Animals↗

Expression of turkey transcription factors and acyl-coenzyme oxidase in different tissues and genetic populations.

Several transcription factors are involved in regulating lipid metabolism in various animal tissues. Peroxisome proliferator-activated receptor (PPAR) gamma and PPARalpha regulate lipogenesis and fatty acid oxidation. Gene fragments for PPARgamma, PPARalpha, and acyl-coenzyme A oxidase (ACO) have been cloned in turkeys, and the sequences of these genes were highly homologous to those of chickens, pigs, and humans. Data showed that turkey PPARgamma and PPARalpha were highly homologous (>97%) with that of the chicken, indicating the genetic relationship between those two species was close. The tissue distribution and genetic effect on mRNA concentrations of PPARgamma, PPARalpha, and ACO in two genetic populations of turkeys [randombred control (RBC2) and growth selected (F line)] was determined. The PPARgamma mRNA was highly expressed in adipose tissue in both populations, but there was no difference between the two populations. The PPARalpha mRNA concentration was high in the liver with less expression in adipose tissue and skeletal muscle. The PPARalpha mRNA concentration was similar between the two genetic populations. The ACO mRNA was expressed in adipose tissue, skeletal muscle, and liver with no difference between the genetic populations. The data suggest that both turkey liver and adipose tissue have considerable capability for fatty acid oxidation and synthesis. Long-term selection for increased 16-wk BW in the F line had no effect on the expression of PPARgamma, PPARalpha, and ACO.

Acyl-CoA Oxidase↗

Possible maternal inheritance of breast muscle morphology in turkeys at sixteen weeks of age.

During the study of inheritance of breast muscle morphology of turkeys during embryonic development and posthatch in two experiments, interesting results were obtained at 16 wk of age. In experiment 1, an experimental line (F) selected long term for increased 16-wk BW was crossed reciprocally with a commercial sire line (B). Samples of pectoralis major muscle were obtained from three males and three females of each genetic group. The F line was reciprocally crossed with a randombred control line (RBC2) in experiment 2, and p. major muscle samples were taken from 10 males and 10 females of each genetic group. The RBC2 line was the base population for the F line. The muscle samples were obtained in a manner to avoid contraction. After fixing, the muscle samples were stained with hematoxylin and eosin to view muscle morphology. Distinct morphological types were observed in the muscle samples for the B, F, and RBC2 lines. The pectoralis major muscle from the B line was, in general, characterized by large fibers with a well-defined extracellular matrix (perimysial and endomysial spaces). Similar to the B line, representative samples of the RBC2 line had a well-defined extracellular matrix but muscle fiber size was not as large as that of the B line. Representative samples of the F line were characterized by a greatly reduced extracellular matrix with the muscle fibers not well defined. For the reciprocal crosses in both experiments, representative samples indicated the offspring had breast muscle morphology similar to that of the female parent, suggesting maternal inheritance. There was no sex effect on breast muscle morphology in either experiment. In order to study the consistency of the results, muscle morphology of representative sections of muscle were subjectively rated by four individuals. The ratings ranged from 1 (little extracellar matrix and indistinct muscle fibers) to 5 (large extracellular space and distinct muscle fibers). Ratings of 2 to 4 were intermediate to these extremes. In experiment 1, ratings of the pure B line and the F sire x B dam cross were similar and higher than that of the pure F line and B sire x F dam cross, which did not differ in average rating. The results for experiment 2 were similar to those for experiment 1 in that the average ratings of the reciprocal crosses were similar to that of the female parental line. The results from the ratings support maternal inheritance of breast muscle morphology.

Animals↗

Effect of selection for growth on onset of sexual maturity in randombred and growth-selected lines of Japanese quail.

An experiment was conducted to determine the effect of selection for growth (BW) on the onset of reproduction (first egg) in Japanese quail hens from growth-selected (HW) and randombred (R1) lines. The HW line had undergone over 40 generations of selection for increased 4-wk BW and was originally developed from the R1 line. Data were collected over two consecutive hatches and summarized by hatch and within lines. Body weight at 35 d of age was positively correlated with BW at sexual maturity (first egg) in both the R1 and HW lines, but these correlations were not significant in both hatches for either line (Hatch 1-R1; Hatch 2-HW; P < or = 0.05). There was a negative correlation between age at sexual maturity (days to first egg) and 35 d BW in both lines with the exception of the HW hens in Hatch 2. Age at sexual maturity and BW at sexual maturity was positively correlated (P < or = 0.001) in the R1 line but did not show the same relationship in the HW line. Age at sexual maturity and weight of the abdominal fat pad were positively correlated in the R1 line (Hatch 1, P < or = 0.01; Hatch 2, P < or = 0.001), but this relationship was not significant in the HW line. Age at sexual maturity and follicle number was negatively correlated in both lines but was not significant in Hatch 2 of the HW line. Follicle size, however, was positively correlated with days to first egg in only Hatch 2 (P < or = 0.001) of the HW line. The data suggest that the relationships between the onset of sexual maturity and both reproductive parameters and carcass traits in hens from consecutive hatches of HW quail are less clear than in the R1 line.

Aging↗

Effect of selection for growth rate on muscle damage during turkey breast muscle development.

Damage to the turkey pectoralis major muscle was studied in a randombred control line (RBC2), a subline (F) from the RBC2 line selected long-term for increased 16-wk BW only, and a commercial sire line (B) at 25 d of incubation and at 1, 4, 8, 16, and 20 wk posthatch. Pectoralis major muscle samples were obtained from three females and three males from each line in a manner to avoid contraction. After being fixed and sectioned, the muscle samples were stained with hematoxylin and eosin to view muscle fiber and muscle fiber bundle morphology. Beginning at 8 wk posthatch, differences in muscle fiber morphology were observed among the different lines. The RBC2 line throughout the duration of the study maintained well-organized muscle fibers and muscle fiber bundles with large capillary networks. In contrast, the growth-selected F line began to show muscle fiber degeneration at 8 wk posthatch, and limited capillary beds were observed as development proceeded. The B line had intermediate muscle morphology between the RBC2 and F lines, but by 20 wk posthatch significant muscle fiber degeneration was present with limited capillary supply. The degenerative muscle fiber changes were predominant in the growth-selected F-line, suggesting that growth selection for just BW may be associated with posthatch muscle damage.

Aging↗

Effect of selection for growth rate and inheritance on posthatch muscle development in turkeys.

The inheritance of, and effect of selection for increased BW on, measurements of muscle fibers and extracellular space in turkeys were studied using a randombred control line (RBC2), a subline (F) of RBC2 selected long-term only for increased 16 wk BW, a commercial sire line (B), and reciprocal crosses of the F and B lines. Measures of additive genetic variation were obtained by comparing all of the pure lines or just the large-bodied F and B lines. Estimates of nonadditive genetic variation were obtained by contrasting the average of the reciprocal crosses with the average of the parental lines. A contrast of the reciprocal crosses provided estimates of sex linkage or maternal effects. Samples of pectoralis major muscle were obtained from three males and three females of each genetic group at 1, 4, 8, and 16 wk of age in a manner to avoid muscle contraction. After fixing and cross sectioning, the muscle samples were stained with hematoxylin and eosin to view muscle morphology. The stained sections were analyzed for muscle fiber width, muscle fiber bundle width (except at 16 wk of age), number of fibers within a 136-microm2 area, and extracellular matrix perimysial (PW) and endomysial (EW) width. Additive genetic variation, as measured by line differences, of measures of muscle fibers and extracellular matrix was a more important source of variation when the RBC2 line was included in the comparison. When all of the pure lines were compared, line differences were significant for fiber bundle width at 4 wk of age; individual fiber width and number of fibers in a given area at 4, 8, and 16 wk of age; PW at all ages; and EW at 1, 8, and 16 wk of age. With the possible exception of PW, nonadditive genetic variation was not an important source of variation for muscle measurements. For PW, the estimates of heterosis were -14.6, 26.4, 14.5, and 17.3% at 1, 4, 8, and 16 wk of age, respectively, but none of the values was significant (P > 0.05). Genetic increases in BW were associated with an increase in muscle fiber width, a smaller number of fibers in a given area, and less extracellular space at older ages. Apparent differences in growth patterns among the genetic groups may have been responsible for the different patterns of change in muscle measurements in the various genetic groups over ages.

Age Factors↗

Effect of selection for growth rate on myosin heavy chain temporal and spatial localization during turkey breast muscle development.

The temporal and spatial localization of the heavy chain fast form of myosin was studied during turkey pectoralis major muscle development in a randombred control line (RBC2), a subline (F) of RBC2 selected only for increased 16-wk BW, a commercial sire line (B), and reciprocal crosses of the F and B lines. Pectoralis major muscle samples were obtained from three females and three males from each group in a manner to avoid contraction. After fixing and sectioning, the muscle samples were stained with a monoclonal antibody to determine the temporal and spatial localization of the heavy chain fast form of myosin. The percentage of muscle fibers at 25 d of incubation and 1 wk posthatch expressing the fast form of myosin heavy chain was calculated. The average percentage of muscle fibers expressing the fast form of myosin heavy chain for all genetic lines combined at embryonic d 25 for males was 76.1 and for females 66.6, whereas at 1 wk posthatch the average percentage for males was 24.2 and 36.1 for females. No interaction of sex and genetic group was noted at either age. At 25 d of embryonic development and at 1 wk of age, additive and nonadditive genetic effects were important in the inheritance of the fast form of myosin heavy chain. Heterosis was negative at both ages but significant at 1 wk of age. By 4 wk posthatch, all the muscle fibers in each genetic group were expressing the myosin heavy chain fast form, and no sex differences were observed. At 16 wk posthatch muscle fiber fragmentation was noted in the samples having reduced endomysial spacing. In the fragmenting muscle fiber areas, expression of the heavy chain fast form of myosin was observed. These muscle fiber changes were predominant in the growth selected F-line suggesting that growth selection may be associated with muscle damage.

Animal Husbandry↗

Developmental expression of skeletal muscle heparan sulfate proteoglycans in turkeys with different growth rates.

Heparan sulfate proteoglycans (HSPG) are a group of extracellular matrix molecules that link skeletal muscle cells to their extrinsic environment. To investigate if HSPG expression is affected by muscle growth and gender, a turkey line (F) selected for increased 16-wk BW and its unselected random-bred control line, RBC2, were used in the present study. Heparan sulfate (HS) and HSPG levels were measured in embryonic and posthatch pectoralis major muscle. HS levels plateaued at embryonic day (ED) 16 in both lines. A significant decrease of HS occurred at ED 18 in F males and females, and at ED 20 and 22 in the RBC2 males and females, respectively. Embryonic HSPG levels peaked at ED 18, and were significantly higher from ED 14 through 18 in F males and females compared with those of the RBC2 line. Male pectoralis major muscle had more HSPG at early embryonic stages than female muscle in both lines. During 1 to 16 wk posthatch, F male and female pectoralis major muscle contained more HSPG than the RBC2 samples, and HSPG levels in F males were higher than those of the females. Myogenic satellite cells derived from F and RBC2 male and female pectoralis major muscle were cultured to measure HSPG expression during proliferation and differentiation. No significant difference in HSPG level was found between the RBC2 and F line cells. However, in both lines, male-derived satellite cells had more HSPG than the female cells during proliferation and differentiation. These data show that HS and HSPG expression are affected by muscle growth properties and sex.

Age Factors↗