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1.
利用微卫星进行奶牛数量性状基因位点定位的研究   总被引:18,自引:0,他引:18  
采用孙女设计法对德国奶牛的3个数量必状--产奶量、乳脂产量及乳蛋白产量进行了数量性状基因位点的定位研究。实验共有20个父系半同胞家系的1130头种公牛,共测定了30对染色体上的229个微卫星,表型性状的育种值由孙代母牛估计得到。连锁分析采用多重遗传标记回归法,临界F值由置换实验法计算得到。统计发现在某些染色体上存在着一些显著的QTL's区域,特别是14号染色体上某一区域对所有3个产奶性状都有极显著  相似文献   

2.
猪的基因图谱及数量性状位点定位   总被引:7,自引:0,他引:7  
在人类基因组计划的带动下,猪的遗传连锁图谱和细胞遗传学图谱有了较大的进步,利用目前猪基因组图谱的研究成果,通过基因组扫描法和候选基因法,可以对猪重要经济性状的主效基因位点进行区域定位,进而图位克隆,找到主效基因,为现代遗传育种奠定理论基础。  相似文献   

3.
唐国庆  李学伟 《遗传学报》2006,33(3):220-229
一种扩展的方法能够在多个世代对具有多个数量性状位点的多性状选择进行最优化。这种方法的基础是在目标雨数中用综合遗传值替代单个性状遗传值,并在整个规划期内最大化所有世代选择反应的加权和。利用多阶段系统优化控制理论,整个最优化问题通过一个向前和向后的迭代循环解决。用一个实际育种猪群的育种参数来评价该方法的选择效果,并和标准QTL选择和常规BLUP选择进行比较。结果表明,优化选择要优于标准QTL选择和常规BLUP选择。经济权重对优化选择的影响较明显,随着达100kg日龄赋予的经济权重的增加,优化选择的优势越明显。优化选择通过两种方式增加总选择反应:1)选择早期减少一部分QTL选择反应;2)对达100kgH龄给予更大的权重。选择后期优化累积贴现选择比优化终端选择给予达100kgH龄更大的权重。  相似文献   

4.
林木数量性状基因定位中的若干问题   总被引:4,自引:0,他引:4  
随着DNA分子标记技术的迅速发展,QTL定位已成为当前生物学研究领域的前沿。身心健康已对许多种动、植物定位了许多重要性状的QTL。这些研究促进了遗传学的发展,并将作为育种的新策略应用。与作物相比,林木QTL定位有其特性。本文详细讨论了林木的生物学特性对QTL定位的影响、QTL定位的系谱设计和统计分析方法。  相似文献   

5.
在猪12号染色体上定位数量性状位点   总被引:3,自引:0,他引:3  
为了找出猪12号染色体上的数量性状位点,在2个家系中测定了10个遗传标记,并记录了51个重要经济性状。该2家系,一个由欧洲野猪与皮特兰杂交而成,另一个由梅山与皮特兰杂交建成。应用最小二乘法进行了数量性状位点定位,同时进行了生长激素基因型与性状间的相关分析。应用最小二乘法并未发现数量性状位点,而应用相关分析发现生长激素基因型与某些膘情性状高度相关。带有基因型C1A2/C4A2的猪比带有基因型C2A2  相似文献   

6.
作物数量性状基因研究进展   总被引:19,自引:0,他引:19  
邢永忠  徐才国 《遗传》2001,23(5):498-502
分子生物技术的发展对作物数量性状基因(QTL)研究提供了条件,不同的定位群体各有其特点,相继出现的QTL定位也逐步完善。大量的研究揭示了QTL的基本特征,剖析了重要农艺4性状的遗传基础,给作物遗传改良带来了新的策略,不断深入的研究已经完成了特定的QTL的精细定位和克隆。本从QTL的定位群体,定位方法,研究现状,精细定位与克隆,以及QTL利用等方面对作物数量性状基因的研究进行了综述。  相似文献   

7.
随着DNA分子标记技术的迅速发展,QTL定位已成为当前生物学研究领域的前沿。迄今已对许多种动、植物定位了许多重要性状的QTL。这些研究促进了遗传学的发展,并将作为育种的新策略应用。与作物相比,林木QTL定位有其特性。本文详细讨论了林木的生物学特性对QTL定位的影响、QTL定位的系谱设计和统计分析方法。  相似文献   

8.
水稻外观品质的数量性状基因位点分析   总被引:26,自引:1,他引:26  
利用由98个家系组成的Nipponbare(粳)/Kasalath(秒)∥Nipponbare回交重组自交系(backcross inbred lines,BILs)群体(BC1F9)及其分子连锁图谱,采用复合区间作图的方法,在2个不同年份对粒长、粒宽、粒形、垩白率、垩白大小、垩白度和透明度等7个稻米外观品质性状的数量性状基因位点(Quantiative trait loci,QTL)进行了定位分析。共定位到33个四QTLs,单个性状QTL数目在4-7个之间,以垩白率最多,为7个;粒长和垩白大小次之,为5个;其他性状均为4个,表明该组合外观品质是由多基因控制的数量性状。单个QTL对性状变异解释率粒长为6.2%-15.2%,粒宽为8.3%-32.5%,长宽比为6.8%-19.8%,垩白率为6.4%-28.5%,垩白大小为6.1%-16.9%,垩白度为9.3%-17.2%,透明度为5.6%-25.2%.QTL在染色体上成集中分布的特点,第3染色体C1488-C563、第5染色体R830-R3166和R1436-R2289、第6染色体R2147-R2171均有3个以上的QTLs分布。比较2年的检测结果表明,外观品质性状的QTL定位都受环境影响,但不同性状受影响的程度差异很大。粒长和粒形的QTL定位受环境影响很小,垩白率、垩白大小和垩白度的QTL定位受环境影响很大。  相似文献   

9.
作物数量性状(QTL)基因研究进展   总被引:1,自引:0,他引:1  
从作物数量性状基因座QTL(quantitative trait locus)作图群体类型及特点,QTL定位的原理和方法,作物QTL研究现状,以及QTL精细定位、克隆、利用等方面进行了综述。对作物QTL分子标记辅助选择育种进行了探讨,并对目前QTL定位中存在的问题和今后QTL的研究方向提出了一些思考。  相似文献   

10.
分子生物技术的发展对作物数量性状基因(QTL)研究提供了条件,不同的定位群体各有其特点,相继出现的QTL定位方法也逐步完善.大量的研究揭示了QTL的基本特征,剖析了重要农艺性状的遗传基础,给作物遗传改良带来了新的策略,不断深入的研究已经完成了特定QTL的精细定位和克隆.本文从QTL的定位群体,定位方法,研究现状,精细定位与克隆,以及QTL利用等方面对作物数量性状基因的研究进行了综述。 Abstract:With the rapid development of molecular biotechnology,QTL analyses were executed for a lot of important agronomic traits in many crops.Different experimental populations and mapping methods had their own advantages in QTL analysis.Amounts of studies paid attention to locate the QTLs for important traits,and others tried to disect the genetic bases using molecular markers.Near isogenic lines were the best populations for QTL fine mapping and positional cloning,A few studies had been reported their results on materials with improvement traits using marker-assisted selection.This paper summarizes the recent progress on QTL mapping populations and methods,the status of QTL locating,QTL fine mapping and positional cloning,and QTL.application in breeding.  相似文献   

11.
Verticillium wilt is one of the most serious constraints to cotton production in almost all of the cotton-growing countries. In this study, "XinLuZaol" (XLZl), a susceptible cultivar Gossypium hirsutum L. and "Hai7124" (H7124), a resistant line G. barbadense, and their F2:3 families were used to map and study the disease index induced by verticillium wilt. A total of 430 SSR loci were mapped into 41 linkage groups; the map spanned 3 745.9 cM and the average distance between adjacent loci was 8.71 cM. Four and five quantitative trait loci (QTLs) were detected based on the disease index investigated on July 22 and August 24 in 2004, respectively. These nine QTLs explained 10.63-28.83% of the phenotypic variance, six of them were located on the D sub-genome. Two QTLs located in the same marker intervals may partly explain the significant correlation of the two traits. QTLs explaining large phenotypic variation were identified in this study, which may be quite useful in cotton anti-disease breeding.  相似文献   

12.
A systems genetics approach combining pathway analysis of quantitative trait loci (QTL) and gene expression information has provided strong evidence for common pathways associated with genetic resistance to internal parasites. Gene data, collected from published QTL regions in sheep, cattle, mice, rats and humans, and microarray data from sheep, were converted to human Entrez Gene IDs and compared to the KEGG pathway database. Selection of pathways from QTL data was based on a selection index that ensured that the selected pathways were in all species and the majority of the projects overall and within species. Pathways with either up- and down-regulated genes, primarily up-regulated genes or primarily down-regulated genes, were selected from gene expression data. After comparing the data sets independently, the pathways from each data set were compared and the common set of pathways and genes was identified. Comparisons within data sets identified 21 pathways from QTL data and 66 pathways from gene expression data. Both selected sets were enriched with pathways involved in immune functions, disease and cell responses to signals. The analysis identified 14 pathways that were common between QTL and gene expression data, and four directly associated with IFNγ or MHCII, with 31 common genes, including three MHCII genes. In conclusion, a systems genetics approach combining data from multiple QTL and gene expression projects led to the discovery of common pathways associated with genetic resistance to internal parasites. This systems genetics approach may prove significant for the discovery of candidate genes for many other multifactorial, economically important traits.  相似文献   

13.

Background

Canine hip dysplasia (CHD) is characterised by a malformation of the hip joint, leading to osteoarthritis and lameness. Current breeding schemes against CHD have resulted in measurable but moderate responses. The application of marker-assisted selection, incorporating specific markers associated with the disease, or genomic selection, incorporating genome-wide markers, has the potential to dramatically improve results of breeding schemes. Our aims were to identify regions associated with hip dysplasia or its related traits using genome and chromosome-wide analysis, study the linkage disequilibrium (LD) in these regions and provide plausible gene candidates. This study is focused on the UK Labrador Retriever population, which has a high prevalence of the disease and participates in a recording program led by the British Veterinary Association (BVA) and The Kennel Club (KC).

Results

Two genome-wide and several chromosome-wide QTLs affecting CHD and its related traits were identified, indicating regions related to hip dysplasia.

Conclusion

Consistent with previous studies, the genetic architecture of CHD appears to be based on many genes with small or moderate effect, suggesting that genomic selection rather than marker-assisted selection may be an appropriate strategy for reducing this disease.

Electronic supplementary material

The online version of this article (doi:10.1186/1471-2164-15-833) contains supplementary material, which is available to authorized users.  相似文献   

14.
The genetic basis of species differences provides insight into the mode and tempo of phenotypic divergence. We investigate the genetic basis of floral differences between two closely related plant taxa with highly divergent mating systems, Mimulus guttatus (large-flowered outcrosser) and M. nasutus (small-flowered selfer). We had previously constructed a framework genetic linkage map of the hybrid genome containing 174 markers spanning approximately 1800 cM on 14 linkage groups. In this study, we analyze the genetics of 16 floral, reproductive, and vegetative characters measured in a large segregating M. nasutus x M. guttatus F2 population (N = 526) and in replicates of the parental lines and F1 hybrids. Phenotypic analyses reveal strong genetic correlations among floral traits and epistatic breakdown of male and female fertility traits in the F2 hybrids. We use multitrait composite interval mapping to jointly locate and characterize quantitative trait loci (QTLs) underlying interspecific differences in seven floral traits. We identified 24 floral QTLs, most of which affected multiple traits. The large number of QTLs affecting each trait (mean = 13, range = 11-15) indicates a strikingly polygenic basis for floral divergence in this system. In general, QTL effects are small relative to both interspecific differences and environmental variation within genotypes, ruling out QTLs of major effect as contributors to floral divergence between M. guttatus and M. nasutus. QTLs show no pattern of directional dominance. Floral characters associated with pollinator attraction (corolla width) and self-pollen deposition (stigma-anther distance) share several pleiotropic or linked QTLs, but unshared QTLs may have allowed selfing to evolve independently from flower size. We discuss the polygenic nature of divergence between M. nasutus and M. guttatus in light of theoretical work on the evolution of selfing, genetics of adaptation, and maintenance of variation within populations.  相似文献   

15.
Detection of quantitative trait loci for growth and fatness in pigs   总被引:1,自引:0,他引:1  
A quantitative trait locus (QTL) analysis of growth and fatness data from a three-generation experimental cross between Meishan (MS) and Large White (LW) pig breeds is presented. Six boars and 23 F1 sows, the progeny of six LW boars and six MS sows, produced 530 F2 males and 573 F2 females. Nine growth traits, i.e. body weight at birth and at 3, 10, 13, 17 and 22 weeks of age, average daily gain from birth to 3 weeks, from 3 to 10 weeks and from 10 to 22 weeks of age, as well as backfat thickness at 13, 17 and 22 weeks of age and at 40 and 60 kg live weight were analysed. Animals were typed for a total of 137 markers covering the entire porcine genome. Analyses were performed using two interval mapping methods: a line-cross (LC) regression method where founder lines were assumed to be fixed for different QTL alleles and a half-/full-sib (HFS) maximum likelihood method where allele substitution effects were estimated within each half-/full-sib family. Both methods revealed highly significant gene effects for growth on chromosomes 1, 4 and 7 and for backfat thickness on chromosomes 1, 4, 5, 7 and X, and significant gene effects on chromosome 6 for growth and backfat thickness. Suggestive QTLs were also revealed by both methods on chromosomes 2 and 3 for growth and 2 for backfat thickness. Significant gene effects were detected for growth on chromosomes 11, 13, 14, 16 and 18 and for backfat thickness on chromosome 8, 10, 13 and 14. LW alleles were associated with high growth rate and low backfat thickness, except for those of chromosome 7 and to a lesser extent early-growth alleles on chromosomes 1 and 2 and backfat thickness alleles on chromosome 6.  相似文献   

16.
17.
A quantitative trait locus (QTL) analysis of carcass composition data from a three-generation experimental cross between Meishan (MS) and Large White (LW) pig breeds is presented. A total of 488 F2 males issued from six F1 boars and 23 F1 sows, the progeny of six LW boars and six MS sows, were slaughtered at approximately 80 kg live weight and were submitted to a standardised cutting of the carcass. Fifteen traits, i.e. dressing percentage, loin, ham, shoulder, belly, backfat, leaf fat, feet and head weights, two backfat thickness and one muscle depth measurements, ham + loin and back + leaf fat percentages and estimated carcass lean content were analysed. Animals were typed for a total of 137 markers covering the entire porcine genome. Analyses were performed using a line-cross (LC) regression method where founder lines were assumed to be fixed for different QTL alleles and a half/full sib (HFS) maximum likelihood method where allele substitution effects were estimated within each half-/full-sib family. Additional analyses were performed to search for multiple linked QTL and imprinting effects. Significant gene effects were evidenced for both leanness and fatness traits in the telomeric regions of SSC 1q and SSC 2p, on SSC 4, SSC 7 and SSC X. Additional significant QTL were identified for ham weight on SSC 5, for head weight on SSC 1 and SSC 7, for feet weight on SSC 7 and for dressing percentage on SSC X. LW alleles were associated with a higher lean content and a lower fat content of the carcass, except for the fatness trait on SSC 7. Suggestive evidence of linked QTL on SSC 7 and of imprinting effects on SSC 6, SSC 7, SSC 9 and SSC 17 were also obtained.  相似文献   

18.
19.
Recently, the use of linkage disequilibrium (LD) to locate genes which affect quantitative traits (QTL) has received an increasing interest, but the plausibility of fine mapping using linkage disequilibrium techniques for QTL has not been well studied. The main objectives of this work were to (1) measure the extent and pattern of LD between a putative QTL and nearby markers in finite populations and (2) investigate the usefulness of LD in fine mapping QTL in simulated populations using a dense map of multiallelic or biallelic marker loci. The test of association between a marker and QTL and the power of the test were calculated based on single-marker regression analysis. The results show the presence of substantial linkage disequilibrium with closely linked marker loci after 100 to 200 generations of random mating. Although the power to test the association with a frequent QTL of large effect was satisfactory, the power was low for the QTL with a small effect and/or low frequency. More powerful, multi-locus methods may be required to map low frequent QTL with small genetic effects, as well as combining both linkage and linkage disequilibrium information. The results also showed that multiallelic markers are more useful than biallelic markers to detect linkage disequilibrium and association at an equal distance.  相似文献   

20.
Mapping quantitative trait loci using the MCMC procedure in SAS   总被引:1,自引:0,他引:1  
S Xu  Z Hu 《Heredity》2011,106(2):357-369
The MCMC procedure in SAS (called PROC MCMC) is particularly designed for Bayesian analysis using the Markov chain Monte Carlo (MCMC) algorithm. The program is sufficiently general to handle very complicated statistical models and arbitrary prior distributions. This study introduces the SAS/MCMC procedure and demonstrates the application of the program to quantitative trait locus (QTL) mapping. A real life QTL mapping experiment in wheat female fertility trait was used as an example for the demonstration. The fertility trait phenotypes were described under three different models: (1) the Poisson model, (2) the Bernoulli model and (3) the zero-truncated Poisson model. One QTL was identified on the second chromosome. This QTL appears to control the switch of seed-producing ability of female plants but does not affect the number of seeds produced once the switch is turned on.  相似文献   

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