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Booroola 系谱的 DNA 指纹分析:对与 Booroola 基因的连锁关系的探索。

DNA fingerprinting analysis of Booroola pedigrees: a search for linkage to the Booroola gene.

机构信息

AgResearch Molecular Biology Unit, Department of Biochemistry and Centre for Gene Research, University of Otago, PO Box 56, Dunedin, New Zealand.

出版信息

Theor Appl Genet. 1993 Oct;87(1-2):271-7. doi: 10.1007/BF00223776.

Abstract

Seven minisatellite probes from a variety of sources were used to analyse 11 paternal half-sib families in which the Booroola gene was segregating. A total of 402 bands that showed segregation in the pedigrees were examined for linkage to the Booroola gene. None of the bands showed segregation with the Booroola gene. The most likely evidence for a linked band was produced by the HaRas HVR probe in Family 902 (θ=0.0; LOD 2.3). The conclusion, however, is that the minisatellite probes used in this study could not be used as markers for the Booroola gene. The study highlighted problems associated with the use of minisatellite probes in linkage studies in half-sib families. The complex banding patterns found on fingerprinting gels was a major source of scoring error. In a few cases both of the sire's alleles could be identified at a particular locus, but in most cases only one of the alleles could be identified. For the most part, the bands had to be treated as dominant alleles. The contribution of dam alleles to the banding pattern could only be estimated. There was an indication that minisatellite loci in sheep are clustered in particular regions of the sheep genome as the rate at which bands segregated with each other was higher than one would expect from loci randomly distributed throughout the genome.

摘要

使用来自不同来源的 7 个微卫星探针分析了 11 个存在 Booroola 基因分离的父半同胞家系。对系谱中显示分离的总共 402 个条带进行了与 Booroola 基因的连锁分析。没有一个条带显示与 Booroola 基因的分离。来自 902 号家系的 HaRas HVR 探针产生了最有可能的连锁带证据(θ=0.0;LOD 2.3)。然而,结论是,本研究中使用的微卫星探针不能用作 Booroola 基因的标记。该研究强调了在半同胞家系的连锁研究中使用微卫星探针所涉及的问题。指纹凝胶上发现的复杂带型是评分错误的主要来源。在某些情况下,可以在特定位置识别出父本的两个等位基因,但在大多数情况下只能识别出一个等位基因。在大多数情况下,这些带必须被视为显性等位基因。只能估计母本等位基因对带型的贡献。有迹象表明,绵羊中的微卫星位点在绵羊基因组的特定区域聚集,因为与每个位点分离的条带的速率高于从基因组中随机分布的位点的预期速率。

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