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通过遗传标记锚定的细菌人工染色体的高分辨率粗线期染色体图谱揭示了水稻第10号染色体着丝粒的位置和遗传重组的分布。

High-resolution pachytene chromosome mapping of bacterial artificial chromosomes anchored by genetic markers reveals the centromere location and the distribution of genetic recombination along chromosome 10 of rice.

作者信息

Cheng Z, Presting G G, Buell C R, Wing R A, Jiang J

机构信息

Department of Horticulture, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Genetics. 2001 Apr;157(4):1749-57. doi: 10.1093/genetics/157.4.1749.

Abstract

Large-scale physical mapping has been a major challenge for plant geneticists due to the lack of techniques that are widely affordable and can be applied to different species. Here we present a physical map of rice chromosome 10 developed by fluorescence in situ hybridization (FISH) mapping of bacterial artificial chromosome (BAC) clones on meiotic pachytene chromosomes. This physical map is fully integrated with a genetic linkage map of rice chromosome 10 because each BAC clone is anchored by a genetically mapped restriction fragment length polymorphism marker. The pachytene chromosome-based FISH mapping shows a superior resolving power compared to the somatic metaphase chromosome-based methods. The telomere-centromere orientation of DNA clones separated by 40 kb can be resolved on early pachytene chromosomes. Genetic recombination is generally evenly distributed along rice chromosome 10. However, the highly heterochromatic short arm shows a lower recombination frequency than the largely euchromatic long arm. Suppression of recombination was found in the centromeric region, but the affected region is far smaller than those reported in wheat and barley. Our FISH mapping effort also revealed the precise genetic position of the centromere on chromosome 10.

摘要

由于缺乏广泛适用且经济实惠、可应用于不同物种的技术,大规模物理图谱构建一直是植物遗传学家面临的重大挑战。在此,我们展示了水稻第10号染色体的物理图谱,该图谱通过细菌人工染色体(BAC)克隆在减数分裂粗线期染色体上的荧光原位杂交(FISH)图谱构建而成。这个物理图谱与水稻第10号染色体的遗传连锁图谱完全整合,因为每个BAC克隆都由一个经遗传定位的限制性片段长度多态性标记锚定。与基于体细胞中期染色体的方法相比,基于粗线期染色体的FISH图谱显示出更高的分辨率。在早期粗线期染色体上,可以分辨出相隔40 kb的DNA克隆的端粒 - 着丝粒方向。遗传重组通常沿着水稻第10号染色体均匀分布。然而,高度异染色质的短臂显示出比主要为常染色质的长臂更低的重组频率。在着丝粒区域发现了重组抑制现象,但受影响的区域远小于在小麦和大麦中报道的区域。我们的FISH图谱构建工作还揭示了第10号染色体着丝粒的精确遗传位置。

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