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应用常染色体上的标记基因研究能够加快数量性状的遗传进展。亲代由标记基因遗传给后代的加性遗传方差值可以用来测定标记基因这种效益。分别在个体水平上以及在复合连续平衡的分离群体水平上建立了标记基因加性遗传方差值的理论方程。这些方程包括与标记基因连锁的数量性状位点数、这些数量性状位点的效应值以及与标记基因有关的重组率。并就分离群体中标记基因加性遗传方差的期望值进行了推导。在分离群体的系谱选择方案中,常染色体上遗传方差中绝大部分与位于该染色体上的标记基因相关。对于牛的一个平均长度染色体来讲,这部分值大约是该染色体孟德尔分离方差值的40% 。标记基因的位置效应和干扰因素对这一期望值的影响是很小的,而染色体的长度对期望方差值影响很大。如果标记基因缺乏多态型以及染色体替代效应估计偏差会大大降低MAS的选择效果。常染色体上标记基因遗传方差期望值的大小表明:即使当标记基因处在一个非活动位点,在分离群体中,仍有较大的染色体替代效应存在。 相似文献
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Abstract. Recent developments in in situγ ray spectrometry offer a new approach to measuring the activity of radionuclides such as 137Cs and 40K in soils, and thus estimating erosion or deposition rates and field moist bulk density (ρm). Such estimates would be rapid and involve minimal site disturbance, especially important where archaeological remains are present. This paper presents the results of a pilot investigation of an eroded field in Scotland in which a portable hyper pure germanium (HPGe) detector was used to measure γ ray spectra in situ. The gamma (γ) photon flux observed at the soil surface is a function of the 137Cs inventory, its depth distribution characteristics and ρm. A coefficient, QCs, derived from the forward scattering of 137Cs γ ray photons within the soil profile relative to the 137Cs full energy peak (662 keV), was used to correct the in situ calibration for changes in the 137Cs vertical distribution in the ploughed field, a function of tillage, soil accumulation and ρm. Based on only 8 measurements, the agreement between in situγ ray spectrometry and soil sample measurements of 137Cs inventories improved from a non significant r2=0.05 to a significant r2=0.62 (P<0.05). Erosion and deposition rates calculated from the corrected in situ137Cs measurements had a similarly good agreement with those calculated from soil cores. Mean soil bulk density was also calculated using a separate coefficient, QK, derived from the forward scattering γ photons from 40K within the soil relative to the 40K full energy peak (1460 keV). Again there was good agreement with soil core measurements (r2=0.64; P<0.05). The precision of the in situ137Cs measurement was limited by the precision with which QCs can be estimated, a function of the low 137Cs deposition levels associated with the weapons testing fallout and relatively low detector efficiency (35%). In contrast, the precision of the in situ ρm determination was only limited by the spatial variability associated with soil sampling. 相似文献
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RAPD技术对地方鸡种群体遗传结构的分析 总被引:16,自引:1,他引:15
利用RAPD技术对4个地方鸡种和1个引进鸡种的群体遗传结构进行分析,通过筛选的5个随机引物OPH-02、OPH-05、OPH-13、OPH-16、OPG-07对5个鸡种的池DNA进行多态性研究,结果表明:5个引物共产生条带61个,扩增产物片段的长度一般从150bp-4kb。 相似文献
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Modern biotechnology promises a number of new applications in animal breeding and production. Although conventional pig breeding has achieved a high level of efficiency and productivity numerous problems have been encountered with animal health and the loss of meat quality. Selection based on phenotypic performance data of individual animals does not take into account the importance of specific genes and their relevance within a complex regulatory system. In most cases it is therefore difficult to trace back the genetic origins of clinically important disorders. The application of genetic engineering techniques in pig production will facilitate diagnosis, improvement of productivity, and animal health by allowing direct genetic manipulation. Attention must be focussed on the physical and genetic analysis of the procine genome. The isolation and characterisation of genes, DNA-markers, polymorphic DNA-fragments, and their chromosomal assignment will be important prerequisites and tools for the elucidation of genetic disorders. Especially the detection of heterozygous carriers of recessive disorders and their elimination from the breeding stock will increase selection accuracy and decrease the generation intervals. But also the rapid and simple detection of infectious diseases, which is sometimes difficult if not impossible at present, will improve animal health and welfare. Although the production of transgenic animals either by DNA-microinjection into zygotes or the use of embryonal stem cells manipulated in vitro is less straightforward than DNA-based diagnosis it will play an important role in the direct manipulation of the porcine genome and genes. Breeding programmes including the use of transgenic livestock have already been developed. There is no doubt that genetic engineering has reached a degree of practical feasibility, allowing it to play an important role in pig breeding in particular and animal production in general. 相似文献
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