共查询到18条相似文献,搜索用时 61 毫秒
1.
根据连锁遗传的原理,列出了三点自交法和两点自交最大似然(ML)法估算显性标记遗传距离的具体步骤和算法,将水稻F2群体含香味基因Aro及其连锁的RFLP数据转变为显性标记数据后,用上述两种方法构建的连锁图谱与用MAPMAKER软件计算共显性数据得到的图谱排序相同、标记间距离相近.但是标记数据存在较大程度偏分离时,由三点自交法构建的图谱中标记间图距有增大趋势.作者为提高作图精确性,简化计算过程,讨论了三点自交法对估算重组值的影响及其在分子标记作图中的应用价值,并建议将共显性标记转变为显性标记时进行两次自交ML法估算。 相似文献
2.
与偏分离位点连锁的QTL作图的统计方法 总被引:2,自引:0,他引:2
提出了一种统计方法,可以估计与偏分离位点连锁的QTL的位置和效应。该方法利用回交群体中呈现偏分离的分子标记,首先用最大似然法对偏分离位点与标记位点之间的重组率和配子存活率进行估计,然后用区间作图法估计加性-显性模型下QTL的位置和效应参数。该方法可用于对常规作图研究中表现偏分离的标记进行分析,以帮助我们发现新的偏分离基因(或不育基因)和数量性状位点。 相似文献
3.
偏分离分子标记的作图方法 总被引:7,自引:0,他引:7
对取自MAPMAKER软件小鼠F_2群体(含333个体)的5个RFLP连锁标记数据作了共显性分子标记偏分离的分析。先确定选择类型的方程组(配子或合子),随后采用Newton-Raphson迭代法估算标记间的重组值。在构建分子标记遗传图谱时,如果两个相邻标记均存在偏分离,最好采用纳入偏分离因子的估算方法。在估计F_2群体标记间偏分离重组距离上,用连续x~2检测方法比传统x~2检测更为准确。 相似文献
4.
不同作图群体对显隐性分子标记位点的作图效率 总被引:2,自引:0,他引:2
根据位点组合和位点的有效性,发展了一种对使用3种不同的作用图群体作图显隐性分子标记的作图效率评价方法,应用该方法所评价的结果是,双单倍体(DH)群体的作图效率最高,自交群体(F2群体)与回交群体的作图效率相同,因此使用双单倍体群体作图不仅所用费用低,而且作图速度快,但只有在极少数植物中能获得双单倍体群体,对于那些不能获得双单倍体的动植物物种而言,可使用自交群体或回交群体作图。如果作高密度的分子标记 相似文献
5.
利用最大似然法进行水稻产量性状基因的分子作图 总被引:10,自引:0,他引:10
本研究根据对估计标记-数量性状基因座位(QTL)之间重组率的两种分析方法(矩量法和最大似然法)、两种方差模型(QTL基因型之间的方差同质和异质模型)的分析,揭示了LOD值在标记-QTL连锁检测上所得结果的相关性高于重组率估计值的相关性。采用最大似然法和异质方差模型,估计了水稻产量构成有关的QTL与分布于11对染色体上的51个限制性片段长度多态性(RFLP)标记之间的重组率,并对似然比(以LOD值表示)进行X ̄2检验,发现7个存在显著连锁关系的标记-性状组合,其平均重组率为10.0%。这些标记分布于第1、5、6、8和11等5对染色体上,涉及7个RFLP标记和3个产量构成性状,即每穗颖花数(RG573、RZ617、RG103)、单株穗数(RG64B)和每穗实粒数(RG101、RG244、RG653)。 相似文献
6.
在雌不发生交换的鳞翅目类昆虫中使用F2群体作图显隐性分子标记连锁图谱的极大似然(ML)法 总被引:5,自引:0,他引:5
在鳞坡目昆虫中,雌性个体的减数分裂细胞不发生遗传重组。这类物种的杂效F2群体中杂合子基因型的与一般物种中雌雄个体的减数分裂细胞都发生遗传重组的F2群体杂合子表型不同,由于这个原因,作用这类物种的遗传连锁图谱通常中使用回交群体。但是,用回效群体傻所得的图谱是不完整的,因为图谱上所有的标记都是百轮回亲本提供的,因此 不会超过杂交F2各体的一半。另外,目前还没有任何方法和软件可以用杂效F2群体来作图鳞翅 相似文献
7.
对取自MAPMAKER软件小鼠F2群体(含333个体)的5个RFLP连锁标记数据作了共显性分子标记偏分离的分析。先确定选择类型的方程组(配子或合子),随后采用Newton-Raphson迭代法估算标记间的重组值。在构建分子标记遗传图谱时,如果两个相邻标记均存在偏分离,最好采用纳入偏分离因子的估算方法。在估计F2群体标记间偏分离重组距离上,用连续χ2检测方法比传统χ2检测更为准确。Abstract The comparative analysis of segregation distortions of the codominant markers data presented in software MAPMAKER are made, where five RFLPs markers involve in a mouse F2 population with 333 individuals. The successive χ2 test begins with the determinations of gametic or zygotic selection types, followed by the estimation of recombination fractions between two markers with the Newton-Raphson iteration method. It is better to use the molecular marker showing segregation distortion for constructing a genetic map, in the case of seriously skew segregation between both the adjoining markers. The successive χ2 test provides better accuracy than that of classical χ2 test for the estimation of the recombination values in F2 population with segregation distortion. 相似文献
8.
远缘杂交中不育基因的位置和效应的最大似然估计 总被引:1,自引:1,他引:1
提出了一种统计方法,利用标记位点的异常分离,来估计远缘杂交中不育基因位点的位置和效应,在回交群体中,用最大似然法对不育基因与标记位点之间的生组值和配子存活率进行估计。将表现连续分布的育性指标转化为百连续变异的遗传标记的分离,可以避免对育性直接观测所带来的重组值估计结果的不稳定,还可以同时估计雌雄配子的存活率。 相似文献
9.
采用最大似然区间定位法对阈模型与一般线性模型的QTL定位效率进行了比较,并对影响离散性状QTL检测效率的主要因素(QTL效应、性状的遗传力和表型发生率)进行了模拟研究,实验设计为多个家系的女儿设计.资源群体大小为500头。研究结果表明:在QTL参数估计及检验功效方面,阈模型方法具有较大的优势,对离散性状QTL定位的效率明显高于LM(Linear Model)方法,定位的准确性也较高。另外,性状遗传力、QTL效应的大小和性状表型发生率对QTL定位的准确度也有直接的影响,随着性状遗传力和表型发生率的提高,随着QTL效应的增大,QTL定位的效率也进一步提高。 相似文献
10.
偏分离是指观察到的基因型比例偏离预期的孟德尔分离频率方式,无法用传统的遗传理论和方法加以分析。偏分离被认为是一种重要的进化动力,并对遗传连锁图谱的构建造成影响。本文针对偏分离的现象、偏分离的影响因素和形成原因,以及对QTL定位的影响等方面进行综合分析,系统阐述了植物分离群体偏分离的研究进展,为后续研究提供有益的参考。 相似文献
11.
12.
Maximum-likelihood models for mapping genetic markers showing segregation distortion. 1. Backcross populations 总被引:4,自引:0,他引:4
M. Lorieux B. Goffinet X. Perrier D. González de León C. Lanaud 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1995,90(1):73-80
A maximum-likelihood approach is used in order to estimate recombination fractions between markers showing segregation distortion in backcross populations. It is assumed that the distortions are induced by viability differences between gametes or zygotes due to one or more selected genes. We show that Bailey's (1949) estimate stays consistent and efficient under more general assumptions than those defined by its author. This estimate should therefore be used instead of the classical maximum-likelihood estimate. The question of detection of linkage is also discussed. We show that the order of markers on linkage groups may be affected by segregation distortion. 相似文献
13.
分子标记在猕猴遗传多样性研究中的应用 总被引:6,自引:2,他引:4
分子标记目前已成为研究遗传多样性的主要工具,为此,简要综述了几种常用的分子标记(RFLPs、RAPD、mtDNA、微卫星DNA、SNPs)的检测方法及其在猕猴种群遗传多样性研究中的应用,为国内猕猴遗传多样性的研究提供参考。 相似文献
14.
Yu JK Kantety RV Graznak E Benscher D Tefera H Sorrells ME 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2006,113(6):1093-1102
Tef [Eragrostis tef (Zucc.) Trotter] is the major cereal crop in Ethiopia. Tef is an allotetraploid with a base chromosome number of 10 (2n = 4x = 40) and a genome size of 730 Mbp. Ninety-four F9 recombinant inbred lines (RIL) derived from the interspecific cross, Eragrostis tef cv. Kaye Murri × Eragrostis pilosa (accession 30-5), were mapped using restriction fragment length polymorphisms (RFLP), simple sequence repeats derived from expressed sequence tags (EST–SSR), single nucleotide polymorphism/insertion and deletion (SNP/INDEL), intron fragment length polymorphism (IFLP) and inter-simple sequence repeat amplification (ISSR). A total of 156 loci from 121 markers was grouped into 21 linkage groups at LOD 4, and the map covered 2,081.5 cM with a mean density of 12.3 cM per locus. Three putative homoeologous groups were identified based on multi-locus markers. Sixteen percent of the loci deviated from normal segregation with a predominance of E. tef alleles, and a majority of the distorted loci were clustered on three linkage groups. This map will be useful for further genetic studies in tef including mapping of loci controlling quantitative traits (QTL), and comparative analysis with other cereal crops.Electronic Supplementary Material Supplementary material is available to authorised users in the online version of this article at . 相似文献
15.
A genetic linkage map of rice was constructed using a double haploid (DH) population from "Gui 630” (Oryza sativa subsp, indica)/"02428" (O. sativa subsp, japonica, wide compatibility variety) and RFLP markers. It consists of 233 loci and covers rice genomes about 2070 cM (centimorgan), and compares well with the other published rice maps. 25 RFLP markers, 2 telomeres and sh-2 (shattering ability) gene were first located on the molecular map of rice. RFLPs between "Gui 630' and "02428' mainly came from base substitution and a few DNA construction variance, not distributed evenly among chromosomes and on chromosome. This was probably resulted from the difference genetic stability among chromosomes and regions, in exchanging recombination ability in different segments of chromosome. 相似文献
16.
实验兔是重要的实验动物之一,在医药领域发挥重要作用。各种分子遗传标记的出现为实验兔系统发育、种群遗传结构分析以及质量控制等各个领域提供了更为简便、可靠的研究手段。但目前,国内实验兔遗传质量不稳定,遗传背景不明确,严重制约着实验兔的应用。本文对各种分子标记在兔遗传多样性中的应用进行综述,以为实验兔遗传检测方法的建立提供帮助。 相似文献
17.
Molecular mapping of the Oregon Wolfe Barleys: a phenotypically polymorphic doubled-haploid population 总被引:18,自引:8,他引:18
J. M. Costa A. Corey P. M. Hayes C. Jobet A. Kleinhofs A. Kopisch-Obusch S. F. Kramer D. Kudrna M. Li O. Riera-Lizarazu K. Sato P. Szucs T. Toojinda M.I. Vales R. I. Wolfe 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2001,103(2-3):415-424
A phenotypically polymorphic barley (Hordeum vulgare L.) mapping population was developed using morphological marker stocks as parents. Ninety-four doubled-haploid lines were
derived for genetic mapping from an F1 using the Hordeum bulbosum system. A linkage map was constructed using 12 morphological markers, 87 restriction fragment length polymorphism (RFLP),
five random amplified polymorphic DNA (RAPD), one sequence-tagged site (STS), one intron fragment length polymorphism (IFLP),
33 simple sequence repeat (SSR), and 586 amplified fragment length polymorphism (AFLP) markers. The genetic map spanned 1,387
cM with an average density of one marker every 1.9 cM. AFLP markers tended to cluster on centromeric regions and were more
abundant on chromosome 1 (7H). RAPD markers showed a high level of segregation distortion, 54% compared with the 26% observed
for AFLP markers, 27% for SSR markers, and 18% for RFLP markers. Three major regions of segregation distortion, based on RFLP
and morphological markers, were located on chromosomes 2 (2H), 3 (3H), and 7 (5H). Segregation distortion may indicate that
preferential gametic selection occurred during the development of the doubled-haploid lines. This may be due to the extreme
phenotypes determined by alleles at morphological trait loci of the dominant and recessive parental stocks. Several molecular
markers were found to be closely linked to morphological loci. The linkage map reported herein will be useful in integrating
data on quantitative traits with morphological variants and should aid in map-based cloning of genes controlling morphological
traits.
Received: 23 August 2000 / Accepted: 15 December 2000 相似文献
18.
Chromosomal regions associated with marker segregation distortion in rice were compared based on six molecular linkage maps.
Mapping populations were derived from one interspecific backcross and five intersubspecific (indica / japonica) crosses, including two F2 populations, two doubled haploid (DH) populations, and one recombinant inbred (RI) population. Mapping data for each population
consisted of 129–629 markers. Segregation distortion was determined based on chi-square analysis (P < 0.01) and was observed at 6.8–31.8% of the mapped marker loci. Marker loci associated with skewed allele frequencies were
distributed on all 12 chromosomes. Distortion in eight chromosomal regions bracketed previously identified gametophyte (ga) or sterility genes (S). Distortion in three other chromosomal regions was found only in DH populations, where japonica alleles were over-represented, suggesting that loci in these regions may be associated with preferential regeneration of
japonica genotypes during anther culture. Three additional clusters of skewed markers were observed in more than one population in
regions where no gametophytic or sterility loci have previously been reported. A total of 17 segregation distortion loci may
be postulated based on this study and their locations in the rice genome were estimated.
Received: 31 May 1996 / Accepted: 30 September 1996 相似文献