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大鼠的高分辨率整合辐射杂种图谱和遗传图谱的一致性连锁图谱。

A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps.

作者信息

Bihoreau M T, Sebag-Montefiore L, Godfrey R F, Wallis R H, Brown J H, Danoy P A, Collins S C, Rouard M, Kaisaki P J, Lathrop M, Gauguier D

机构信息

The Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford OX3 7BN, UK.

出版信息

Genomics. 2001 Jul;75(1-3):57-69. doi: 10.1006/geno.2001.6583.

Abstract

We have constructed a high-resolution consensus genetic map of the rat in a single large intercross, which integrates 747 framework markers and 687 positions of our whole-genome radiation hybrid (RH) map of the rat. We selected 136 new gene markers from the GenBank database and assigned them either genetically or physically to rat chromosomes to evaluate the accuracy of the integrated linkage-RH maps in the localization of new markers and to enrich existing comparative mapping data. These markers and 631 D-Got- markers, which are physically mapped but still uncharacterized for evidence of polymorphism, were tested for allele variations in a panel of 16 rat strains commonly used in genetic studies. The consensus linkage map constructed in the GK x BN cross now comprises 1620 markers of various origins, defining 840 resolved genetic positions with an average spacing of 2.2 cM between adjacent loci, and includes 407 gene markers. This whole-genome genetic map will contribute to the advancement of genetic studies in the rat by incorporating gene/EST maps, physical mapping information, and sequence data generated in rat and other mammalian species into genetic intervals harboring disease susceptibility loci identified in rat models of human genetic disorders.

摘要

我们通过一个单一的大型杂交构建了大鼠的高分辨率一致性遗传图谱,该图谱整合了747个框架标记和大鼠全基因组辐射杂种(RH)图谱中的687个位置。我们从GenBank数据库中选择了136个新的基因标记,并通过遗传或物理方法将它们定位到大鼠染色体上,以评估整合的连锁-RH图谱在新标记定位中的准确性,并丰富现有的比较图谱数据。在一组常用于遗传研究的16个大鼠品系中测试了这些标记以及631个D-Got-标记(已进行物理定位但仍未鉴定出多态性证据)的等位基因变异。在GK×BN杂交中构建的一致性连锁图谱现在包含1620个不同来源的标记,定义了840个解析的遗传位置,相邻位点之间的平均间距为2.2 cM,并包括407个基因标记。通过将基因/EST图谱、物理图谱信息以及在大鼠和其他哺乳动物物种中生成的序列数据纳入在人类遗传疾病大鼠模型中鉴定出的携带疾病易感性位点的遗传区间,这个全基因组遗传图谱将有助于推进大鼠的遗传研究。

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