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检测分离群体杂交中标记基因座与影响数量性状基因座之间的连锁关系。

Detection of linkage between marker loci and loci affecting quantitative traits in crosses between segregating populations.

机构信息

Department of Plant Genetics and Breeding, Agricultural Research Organization, The Volcani Center, 50250, Bet Dagan, Israel.

出版信息

Theor Appl Genet. 1988 Aug;76(2):228-36. doi: 10.1007/BF00257850.

Abstract

By making use of pedigree information and information on marker-genotypes of the parent and F-1 individuals crossed to form an F-2 population, it is possible to carry out a linkage analysis between marker loci and loci affecting quantitative traits in a cross between segregating parent populations that are at fixation for alternative alleles at the QTL, but share the same alleles at the marker loci. For two-allele systems, depending on marker allele frequencies in the parent populations, 2-4 times as many F-2 offspring will have to be raised and scored for markers and quantitative traits in order to provide power equivalent to that obtained in a cross between fully inbred lines. Major savings in number of F-2 offspring raised can be achieved by scoring each parent pair for a large number of markers in each chromosomal region and scoring F-1 and F-2 offspring only for those markers for which the parents were homozygous for alternative alleles. For multiple allele systems, particularly when dealing with hypervariable loci, only 10%-20% additional F-2 offspring will have to be raised and scored to provide power equivalent to that obtained in a cross between inbred lines. When a resource population contains novel favorable alleles at quantitative trait loci that are not present (or rare) in a commercial population, analyses of this sort will enable the loci of interest to be identified, mapped and manipulated effectively in breeding programs.

摘要

通过利用家系信息以及亲本个体的标记基因型信息和 F1 个体杂交形成 F2 群体,可以对分离亲本群体杂交中受数量性状基因座影响的标记基因座与基因座之间进行连锁分析,这些亲本群体在 QTL 处处于替代等位基因的固定状态,但在标记基因座处具有相同的等位基因。对于二倍体系统,根据亲本群体中标记等位基因的频率,需要多培育和标记 2-4 倍的 F2 后代,才能获得与完全自交系杂交获得的等效功效。通过在每个染色体区域对每个亲本对进行大量标记的评分,并仅对那些父母为替代等位基因纯合的标记对 F1 和 F2 后代进行评分,可以在数量上大大节省培育的 F2 后代数量。对于多倍体系统,特别是在处理高度多态性的基因座时,仅需要额外多培育和标记 10%-20%的 F2 后代,就可以提供与自交系杂交获得的等效功效。当资源群体中存在商业群体中不存在(或罕见)的数量性状基因座的有利新等位基因时,此类分析将能够有效地识别、定位和操作感兴趣的基因座,从而应用于育种计划。

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