共查询到18条相似文献,搜索用时 187 毫秒
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DNA标记与动物杂种优势的关系研究进展 总被引:3,自引:0,他引:3
传统的杂种优势预测方法和杂种优势理论的缺陷限制了杂种优势的进一步利用。分子标记为杂种优势的预测和理论发展开辟了新领域。本文论述了分子标记的种类和影响分子标记预测杂种优势的因素及其在动物杂种优势研究中的应用。 相似文献
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杂种优势与分子标记关系的研究 总被引:4,自引:0,他引:4
大量存在的分子标记及其丰富的遗传变异,可以应用于辅助鉴定杂交亲本的选择以及杂种优势的预测。笔者对DNA分子标记中的一种RAPD技术以及关于杂种优势与杂种优势的预测方面作了综述。 相似文献
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三个鸡品系的遗传差异与杂种优势关系的研究 总被引:1,自引:0,他引:1
采用RAPD标记分析了武定鸡快羽系、绿壳蛋系和合成系间的遗传差异,进行了三个鸡品系间的杂交试验,并应用简单的线性相关分析了遗传距离指数与杂种优势的关系。分析结果表明快羽系与绿壳蛋系间的遗传差异较小,而快羽系与合成系间的遗传差异较大。品系间遗传距离指数与F1代各性状观察值均为正相关,但相关不显著;与杂种优势率之间也均为正相关,但只与13周龄存活率、种蛋受精率有显著的相关关系。表明RAPD标记在预测杂种优势上具有一定参考价值。 相似文献
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肉牛杂交亲本遗传距离与杂种优势的相关性研究 总被引:2,自引:0,他引:2
利用11个微卫星标记研究川南山地黄牛、海福特牛、黑安格斯牛、红安格斯牛、利木赞牛、西门塔尔牛、德国黄牛的遗传多样性,分析肉牛亲本间微卫星标记遗传距离与体尺、体重杂种优势间的相关性。结果表明:11个微卫星基因座平均有效等位基因数为4.5422,7个牛种的多态信息含量在0.3434~0.4207,平均杂合度为0.6868~0.8413,7个牛种均具有丰富的多态性。亲本间遗传距离与体尺、体重杂种优势间相关系数偏小(-0.003~0.304),均未达到显著水平,用微卫星标记遗传距离预测肉牛体尺、体重杂种优势还有待进一步探讨。 相似文献
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A K Sheridan 《British poultry science》1986,27(4):541-550
The heterosis inheritance backcross evaluation technique (HI-BET) is proposed as a selection strategy for developing a pair of complementary strains from a crossbred population descended from a F1 population possessing considerable heterosis. These complementary strains are expected to produce a strain cross superior to the F1 population from which they were derived. In the first stage of an experimental evaluation of HI-BET, Australorp and White Leghorn hens were compared with their F1, F2 and F1 by parental breed backcross populations for a range of egg production traits. The substantial heterosis for survivors' egg production and total egg mass was largely lost in the F2 and backcross populations indicating that this heterosis was mainly due to parental epistasis. The uneven distribution of residual heterosis in the backcross populations suggests that about two-thirds of this parental epistasis was inherited from the White Leghorn line. As the Australorp line was substantially superior to the White Leghorn line for survivors' egg production and total egg mass, it most likely contained additive genes for both these traits that were not present in the White Leghorn line. It is suggested that HI-BET should be an effective strategy for incorporating these additive genes into the White Leghorn line, together with some brown egg shell genes if also desired, as a means of further improving the performance of the F1 cross. 相似文献
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By F. Minvielle J. -L. Monvoisin J. Costa A. Frenot Y. Maeda 《Zeitschrift für Tierzüchtung und Züchtungsbiologie》1999,116(5):363-377
In much animal production, commercial animals are crossbreds from closed lines or breeds under long-term directional selection. Therefore it is desirable to be able to predict heterosis gains over the generations as it is done for genetic progress under within-line selection. However, heterosis is the phenotypic expression of a complex phenomenon which may involve several types of genetic effects like dominance and epistasis. In animal breeding, basic quantitative genetics theory indicates that heterosis should be proportional to (squared) differences in gene frequency between populations (e.g. F alconer and M ac K ay 1996), and it has been found approximately correct, so it is commonly used for planning crosses. Under that type of heterosis, however, selection towards the same objective in two populations should bring gene frequencies closer, and therefore it should eventually decrease heterosis. On the other hand, reciprocal recurrent selection designed to increase genetic distance between lines should eventually achieve maximum heterosis (O llivier 1982). Some experiments reviewed by brun (1982) have already compared genetic progress under within-line and reciprocal recurrent selection, but they did not focus on comparing the trend of heterosis with generations between the two selection methods. Also, heterosis was monitored periodically in some selection experiments on poultry, and results were reviewed by F airfull (1990). They were somewhat contradictory, but they generally failed to relate genetic progress to loss of heterosis under within-line selection. Moreover, in commercial production, as purebreds and crossbreds are not contemporaries and are generally maintained under very different management systems, estimations of heterosis and of the evolution of crossbred advantage over the generations may be difficult to obtain. Using the Japanese quail as an experimental animal, the present work was initiated specifically to follow the changes in heterosis brought about by selection for a single heterotic trait, early egg production (M invielle et al. 1995). For that purpose, two selection methods expected to have opposite effects on heterosis, directional within-line (or individual) selection and reciprocal recurrent selection, were applied for 13 generations in four quail lines started from two different origins, and trends of heterosis in the selected character and in weight and egg traits were evaluated. 相似文献
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K A Leymaster 《Journal of animal science》1987,65(1):110-116
Crossbreeding of sheep is practiced to exploit simultaneously the use of additive and nonadditive genetic effects. The goal is to achieve optimal levels of performance appropriate for defined systems of sheep production and marketing. Although the beneficial effects of individual and maternal heterosis on sheep production have been well documented and widely implemented, considerably less is known about the effects of paternal heterosis. Limited evidence suggests that crossbred rams are more sexually aggressive and exhibit greater testicular growth than do purebred rams. Average estimates of paternal heterosis effects were 1.4, -.7 and 2.3% for seasonal fertility, prolificacy and preweaning survival, respectively. The average effect of paternal heterosis on fertility during spring breeding was 29.5%. Progeny of crossbred and purebred sires were similar in birth weight, weaning weight and postweaning growth rate and in phenotypic variation for these growth traits. However, favorable paternal heterosis effects need not exist to warrant the use of crossbred sires. Composite or F1 sires can be used as an effective method to manage the composition of additive breed effects. For example, varying proportions of germ plasm from highly prolific breeds such as the Finnsheep and Romanov can be realized through the use of crossbred sires to set reproductive rates at desired levels. Crossbred sires may be used to a greater extent to optimize additive breed effects than to exploit effects of paternal heterosis. The role of composite breeds in managing both additive and nonadditive effects is discussed. 相似文献
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1. Inbreeding and heterosis effects for quantitative traits were estimated in two White Leghorn lines selected with reciprocal recurrent selection (RRS) since 1950. 2. Pedigreed progeny were produced from full-sib, half-sib and unrelated pure line as well as reciprocal cross line matings to estimate inbreeding and heterosis effects "within sires". 3. Inbreeding effects estimated as linear regressions agreed well with estimates considering inbreeding as fixed effect. The inbreeding depression per 10% inbreeding was highest for hatchability (6-7%), intermediate for production-related traits (3%), and about 1% for shell quality, body weight and egg weight. 4. Heterosis effects were estimated by comparing pure line and cross line progeny of the same sires. 5. Results indicate considerably less heterosis for egg production than found earlier, which is interpreted as a consequence of pure line selection. 相似文献