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1.
应用RAPD标记构建马尾松单株树遗传连锁图谱   总被引:5,自引:0,他引:5  
利用马尾松(Pinusmassoniana)崇义群体C-16号单株上40粒种子的胚乳为作图群体材料,用随机扩增多态性DNA(RAPD)方法构建马尾松单株遗传连锁图谱,从被步筛选的80个引物中,得到16个具有多态性产物的引物,对这16种引物进行Mendelian1:1分离检测(卡方检验,P<0.05),我们得到符合Mendelian1:1分离比例的RAPDs标记49个.通过对49个标记的连锁关系进行分析,其中29个标记分布在12个连锁群上,总图距为483.3cM,平均图距为28.42cM,20个标记没有连锁到任何连锁群上,需要继续进行大量标记的连续分析,构建完善的高密度的遗传图谱,使之能够对数量性状位点QTLs进行定位,从而进行分子标记辅助选择育种(MAS).  相似文献   

2.
使用美国五大学射电天文台(FCRAO)的14m无线和新建立的QUARRY接收系统对中心区CO(2-1)谱线呈现双峰特征的2个PMS星P11和V1515Cyg进行了CO(1-0)的谱线成图观测。观测表明,无论是PP11还是V1515Cyg,其CO(1-0)谱线都在大范围内表现出双峰谱型。分析PP11和V1515Cyg红、蓝2个速度峰和峰谷速度上的等强分布可以发现,与主序前星成协且具有CO双峰谱的分子云中可能存在2种运动:一种是低速的与视线方向成某个角度的大张角的双向运动,它可能是PMS星形成前双极外向流阶段的进一步发展(张角变大,速度变小);另一种是起因于PMS星风的向四外发展的膨胀的壳层运动,而在壳层内密度分布是高度团块性的,这种团块可能是新形成的PMS星与母分子云相互作用,从而导致分子云碎裂的结果。  相似文献   

3.
Two telomere-associated sequences (TAS), named STAS8 and STAS10, were cloned from soybean genomic DNA using polymerase chain reaction (PCR) amplification. Southern analysis showed that they were sequences with moderate copy number in soybean genome. Sequence analysis demonstrated that STAS10 had tandemly arrayed con sensus sequences of TTTAGGG and TIAGGG . The mapping of these two TAS was performed with a population of F8 re combinant inbred line using restriction fragment length polymorphisms(RFLP). Seven out of nine polymorphic fragments were mapped to the most distal position of five linkage groups, Dla, F, G2, H and Q of soybean, and the other two loci were closely linked and mapped to two interstitial positions within linkage group D1a. The mapping of TAS in soybean is essential for completeness of a molecular genetic map of soybean.  相似文献   

4.
小麦雌性育性双向极端群体QTL定位策略初探   总被引:1,自引:0,他引:1  
在极端不育群体中计算重组频率(c值)初步筛选QTL位点的基础之上,利用普通小麦中育性正常的良种藁城8901(P1)与雌性不育系XND126(P2)杂交F2群体中的189株隐性极端不育株和63株极端可育株组成的双向极端群体为定位群体,构建了连锁图,分析定位了小麦雌性育性位点taf1,获得了与F2平衡群体相同的定位位点.分析发现与taf1位点连锁较紧密的标记,其c值较小.利用极端群体的策略能快速有效的定位小麦雌性育性QTL在染色体上的位置.  相似文献   

5.
Quantitative trait loci (QTLs) controlling salt-tolerance at the seedling stage in rice (Oryza sativa L.) were identified by interval mapping (SIM) and composite interval mapping (CIM) using a doubled haploid population ZJDH and its high resolution genetic linkage map. The population was derived from an inter-subspecific cross between an indica variety Zhaiyeqing8 (ZYQ8) and a japonica variety Jingxi17 (JX17). Analysis of survival days of seedlings treated with 0.7% NaCI revealed that a major salt-tolerance quantitative trait locus (QTL), Std, was present between markers RG612 and C131 on chromosome 1 when using both MAPMAKER/QTL 1.1 and PLABQTL 1.0 (SIM). Its allele which contributes to salt-tolerance was from ZYQ8. In addition, seven more QTLs which give additive effect on salt-tolerance are identified when using PLABQTL (CIM), and most of them were from JX17.  相似文献   

6.
Non-Mendelian segregation of markers, known as distorted segregation, is a common biological phenomenon. Although segregation distortion affects the estimation of map distances and the results of quantitative trait loci (QTL) mapping, the effects of distorted markers are often ignored in the construction of linkage maps and in QTL mapping. Recently, we have developed a multipoint method via a Hidden Markov chain method to reconstruct linkage maps in an F2 population that corrects for bias of map distances between distorted markers. In this article, the method is extended to cover backcross, doubled haploid and recombinant inbred line (RIL) populations. The results from simulated experiments show that: (1) the degree that two linked segregation distortion loci (SDL) affect the estimation of map distances increases as SDL heritability and interval length between adjacent markers increase, whereas sample size has little effect on the bias; (2) two linked SDL result in the underesti- mation of linkage distances for most cases, overestimation for an additive model with opposite additive effects, and unbiased estimation for an epistatic model with negative additive-by-additive effects; (3) the proposed method can obtain the unbiased estimation of linkage distance. This new method was applied to a rice RIL population with severely distorted segregation to reconstruct the linkage maps, and a bootstrap method was used to obtain 95% confidence intervals of map distances. The results from real data analysis further demonstrate the utility of our method, which provides a foundation for the inheritance analysis of quantitative and viability traits.  相似文献   

7.
以国际小麦作图组织的重组自交系群体W7984×Opata85为材料,在两种不同试验环境(2009年天津东丽区、2009年天津西青区姚村)下,分析其亲本及114个株系群体的株高,并利用QTL作图软件WinQTLCart2.5和区间作图及复合区间作图方法,对控制小麦株高性状的QTL进行定位.共检测到4个与小麦株高相关的QT...  相似文献   

8.
遗传作图软件应用及辅助软件的研制   总被引:4,自引:2,他引:2  
介绍了当前普遍用于遗传图谱构建和QTL定位的软件MAPMAKER3.0(forPC)的功能、数据结构和基本操作命令与步骤;指出了该软件存在的问题与不足。介绍了作者开发的用于遗传图谱构建中方便研究者建立符合MAPMAKER要求的分析数据文件,以及对标记的分离比进行检验的辅助软件MDAC。提出了进一步开发中文版新一代遗传作图软件、建立基因组图谱数据库和基于因特网(Internet)的基因组信息检索等设想。  相似文献   

9.
Awnness is a key trait in rice domestication, yet no studies have been conducted on fine mapping or association mapping of the rice awn gene. In this study, we investigated the awnness and genotype of a core collection of 303 cultivated rice varieties and a BC5F2 segregating population of 200 individuals. Combining association and linkage analyses, we mapped the awnness related genes to chromosome 4. Primary association analysis using 24 SSR markers revealed five loci significantly associated with awnness on chromosome 4. The associated markers cover previously identified regions. Fine association mapping was conducted using another 29 markers within a 4-Mb region, covering the associated marker in34, which is close to the awn gene Awn4.1. Seven associated markers were revealed, distributed over an 870-kb region. Combining the fine association mapping and linkage analysis of awnness in the 200 BC5F2 segregating population, we finally identified a 330-kb region as the candidate region for Awn4.1. The results indicate that combining association mapping and linkage mapping provides an efficient and precise approach to both genome-wide mapping and fine mapping of rice genes.  相似文献   

10.
The fragile rice mutant was isolated from an M2 population of indica variety Shuang Ke Zao (SKZ) treated with g-rays, and designated as fp1 (fragile plant 1) because of its fragile leaves and culms. To map FP1 locus, an F2 mapping population was derived from a cross between the fp1 and C-bao, a polymorphic japonic variety. The primary mapping result places the FP1 locus in an interval between two molecular markers, microsatellite marker RM16 (3.1 cM proximal to FP1) and STS marker G144a (9.1 cM distal to FP1) in the centromere region of chromosome 3. A CAPS marker C524a was further developed between RM16 and G144a, with 0.4 cM genetic distances to the FP1locus, providing a practical starting point for constructing a BAC contig spanning the FP1 locus and cloning the fp1 gene. Allelism test demonstrated that fp1 is allelic to bc1, a fragile rice mutant reported previously.  相似文献   

11.
Many QTL mapping methods have been developed in the past two decades.Statistically,the best method should have a high detection power but a low false discovery rate (FDR).Power and FDR cannot be derived theoretically for most QTL mapping methods,but they can be properly evaluated using computer simulations.In this paper,we used four genetic models (two for independent loci and two for linked loci) to illustrate power and FDR estimation for interval mapping (IM) and inclusive composite interval mapping (ICIM).For each model,we simulated 1000 populations each of 200 doubled haploids.A support interval (SI) was first defined to indicate to which predefined QTL the significant QTL belonged.Power was calculated by counting the number of simulation runs with significant peaks higher than the logarithm of odds (LOD) threshold in the SI.Quantitative trait loci not identified in any SIs were viewed as false positives.The FDR is the rate at which QTLs are identified as significant when they are actually non-significant.Simulation results allowed us to estimate power and FDR of IM and ICIM for two independent and two linkage genetic models.Our estimates allowed us to readily compare the efficiencies of different statistical methods for QTL mapping,including the ability to separate linkage,under a wide range of genetic models.We used IM and ICIM as examples of how to estimate power and FDR,but the principles shown in this paper can be used for power analysis and comparison of any other QTL mapping methods,especially those based on interval tests.  相似文献   

12.
【目的】传统的数量性状基因座(QTL)定位统计分析方法是针对自交系产生实验群体而建立的,不能直接应用到林木这种杂合度较高生长周期较长的异交物种中。针对林木多元性状数据,将传统的QTL区间作图方法应用到林木杂交F1代作图群体中。【方法】考虑分子标记各种可能的分离比以及连锁相信息,建立林木多元性状数据QTL定位统计分析模型,并用R语言编写了相应的计算软件包mvqtlmap。在美洲黑杨和小叶杨杂交F1代群体中,对2014年5月29日至9月24日期间调查的6个时间点树高数据进行了QTL定位分析。【结果】有4个QTL定位在母本美洲黑杨的遗传连锁图谱上,有6个QTL分布在父本小叶杨的遗传连锁图谱上,这些QTL分别位于第1、5、7、9、11和19号染色体上,平均解释0.8%~6.7%的表型方差。【结论】研究结果可为在林木上利用多个性状或多个时间点性状数据进行QTL定位提供统计分析方法及计算工具。所建立的程序包可在网站http://www.bioseqdata.com/mvqtlmap/mvqtlmap.htm上自由下载。  相似文献   

13.
以拟南芥黑胫病感病突变体及抗病野生型为材料,对不同世代群体进行遗传分析,结果表明,该突变性状为细胞核内两对重叠作用的基因所控制,感病植株为隐性突变体,其基因型为sc1sc2.同时对突变位点sc1及sc2进行了染色体定位研究.结果证实, sc1位于1号染色体的长臂上,sc2位于2号染色体的长臂上.为进一步研究拟南芥抗病功能基因奠定了基础.  相似文献   

14.
Understanding linkage disequilibrium (LD) created in admixed population and the rate of decay in the disequilibrium over evolution is an important subject in population genetics theory and in disease gene mapping in human populations. The present study represents the theoretical investigation of effects of gene frequencies, levels of LD and admixture proportions of donor populations on the evolutionary dynamics of the LD of the admixed population. We examined the conditions under which the admixed population reached linkage equilibrium or the peak level of the LD. The study reveals the inappropriateness in approximating the dynamics of the LD generated by population admixture by the commonly used formula in literature. An appropriate equation for the dynamics is proposed. The distinct feature of the newly suggested formula is that the value of the nonlinear component of the LD remains constant in the first generation of the population evolution. Comparison between the predicted disequilibrium dynamics shows that the error will be caused by using the old formula, and thus resulting in a misguidance in using the evolutionary information of the admixed population in gene mapping.  相似文献   

15.
Genetic analysis and fine mapping of genes controlling leaf rolling were conducted using two backcrossed generations (BC4F2, BC4F3) derived from a cross between QMX, a non-rolled leaf cultivar as a recurrent parent, and JZB, a rolled leaf NIL of ZB as a donor parent. Results indicated that leaf rolling was mainly controlled by an incompletely recessive major gene, namely rl(t), and at the same time, affected by quantitative trait loci (QTLs) and/or the environment. A genetic linkage map was constructed using MAPMAKER/EXP3.0 with eight polymorphic markers on chromosome 2, which were screened by BAS method from 500 SSR markers and 15 newly developed insertion/deletion (InDel) markers. The position of rl(t) was estimated with composite interval mapping (CIM) method using WinQTLcart2.5. Gene rl(t) was mapped between markers InDel 112 and RM3763, and 1.0 cM away from InDel 112 using 241 plants in BC4F2 population. To fine map r(t), one BC4F3 line with 855 plants was generated from one semi-rolled leaf plant in BC4F2. Four new polymorphic InDel markers were developed, including InDel 112.6 and InDel 113 located between markers InDe1112 and RM3763. Based on the information of recombination offered by 191 rolled leaf plants and 185 non-rolled leaf plants from the BC4F3 line ,we mapped r(t) to a 137-kb region between markers InDel 112.6 and InDel 113. Homologous gene analysis suggested that r(t)was probably related to the process of leaf development regulated by microRNA.  相似文献   

16.
Quantitative trait locus (QTLs) mapping for rapid visco analyser (RVA) profile parameters has been carried out by using a double haploid (DH) population derhred from a cross betweenindica variety Zhai-Ye-Qing 8 andjaponica variety Jing-Xi 17 and its genetic linkage map. The results indicate that the segregation of the RVA profiles is continually distributed among the DH lines, and some DH lines show transgressive segregation for all the parameters. A major QTL,Waxy (Wx) gene on chromosome 6 which controls the amylose synthesis, has been detected significantly for 5 traits: hot paste viscosity (HPV), cool paste viscosity (CPV), breakdown viscosity (BDV), consistency viscoslty (CSV) and setback viscoslty (SBV). Therefore, the RVA profile parameters are mainly controlled byWx gene. Other 3 and 2 QTLs have also been identified for BDV and SBV, respectively, and two of them share the same region on chromosomes 1 and 5. However, the peak viscosity (PKV) is controlled by a minor QTL on chromosome 12, qPKV-12.  相似文献   

17.
IntroductionsIn 2000, Ian Foster refined the definition [1] of Grid as“resource sharing and coordinated problem solving indynamic, multi institutional virtual organizations”. WithOGSA (Open Grid Service Architecture) [2] as its systemframework, OGSI (Open Grid Services Infrastructure) [3]as its implement mechanism and GT3 ( GlobusToolkit3.0) [4] as its development software, Grid is nowbecoming a newparadigm for solvinglarge scale distributedresource …  相似文献   

18.
Cucumber (Cucumis sativus L.) is an annualclimber originated from the tropic rain forest area inthe south of Himalayas, which belongs to the Cucur bitaceae family. Cucumber is one of the importantvegetables in the world, and its planting area is sec ond only to that of tomato[1]. However genetics re search on cucumber obviously drops behind that of thelatter. The classic genetic map of cucumber, with sixlinkage groups, is composed of more than 100 genesfor color, morphology, and dise…  相似文献   

19.
Triploids,recognized to occur more frequently in natural and experimental populations of many species than previously appreciated,display important economic and biological values.Despite this,however,linkage analysis for triploids has not been well explored.We develop a statistical model for estimating and testing the linkage between molecular markers in a triploid population derived from a tetraploid and diploid parent.The model incorporates one important meiotic feature of tetraploids by which more homologous chromosomes pair with a greater likelihood than less homologous chromosomes.By implementing the EM algorithm within the maximum likelihood framework,the model provides a procedure for simultaneous estimation of the linkage and preferential pairing factor.The model accommodates the segregating patterns of pseudotest markers and intercross markers with different amounts of informativeness.The utility of the model was validated through a real data analysis and simulation studies.The model provides a statistical tool for linkage analysis in a triploid population by taking into account meiotic behavior of tetraploids.Results from the model will help to shed light on the genetic diversity and origin of a polyploid population.  相似文献   

20.
INSULIN-dependent (type I) diabetes mellitus (IDDM) follows an autoimmune destruction of the insulin-producing beta-cells of the pancreas. Family and population studies indicate that predisposition is probably polygenic. At least one susceptibility gene lies within the major histocompatibility complex and is closely linked to the genes encoding the class II antigens, HLA-DR and HLA-DQ (refs 3, 4). Fine mapping of susceptibility genes by linkage analysis in families is not feasible because of infrequent recombination (linkage disequilibrium) between the DR and DQ genes. Recombination events in the past, however, have occurred and generated distinct DR-DQ haplotypes, whose frequencies vary between races. DNA sequencing and oligonucleotide dot-blot analysis of class II genes from two race-specific haplotypes indicate that susceptibility to IDDM is closely linked to the DQA1 locus and suggest that both the DQB1 (ref. 7) and DQA1 genes contribute to disease predisposition.  相似文献   

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