Institute of Botany, Dresden University of Technology, Zellescher Weg 20b, 01217 Dresden, Germany.
Plant J. 2012 Nov;72(4):600-11. doi: 10.1111/j.1365-313X.2012.05102.x. Epub 2012 Sep 7.
We developed a reference karyotype for B. vulgaris which is applicable to all beet cultivars and provides a consistent numbering of chromosomes and genetic linkage groups. Linkage groups of sugar beet were assigned to physical chromosome arms by FISH (fluorescent in situ hybridization) using a set of 18 genetically anchored BAC (bacterial artificial chromosome) markers. Genetic maps of sugar beet were correlated to chromosome arms, and North-South orientation of linkage groups was established. The FISH karyotype provides a technical platform for genome studies and can be applied for numbering and identification of chromosomes in related wild beet species. The discrimination of all nine chromosomes by BAC probes enabled the study of chromosome-specific distribution of the major repetitive components of sugar beet genome comprising pericentromeric, intercalary and subtelomeric satellites and 18S-5.8S-25S and 5S rRNA gene arrays. We developed a multicolor FISH procedure allowing the identification of all nine sugar beet chromosome pairs in a single hybridization using a pool of satellite DNA probes. Fiber-FISH was applied to analyse five chromosome arms in which the furthermost genetic marker of the linkage group was mapped adjacently to terminal repetitive sequences on pachytene chromosomes. Only on two arms telomere arrays and the markers are physically linked, hence these linkage groups can be considered as terminally closed making the further identification of distal informative markers difficult. The results support genetic mapping by marker localization, the anchoring of contigs and scaffolds for the annotation of the sugar beet genome sequence and the analysis of the chromosomal distribution patterns of major families of repetitive DNA.
我们为普通甜菜开发了一个参考核型,适用于所有甜菜品种,并为染色体和遗传连锁群提供了一致的编号。通过使用一组 18 个遗传锚定的 BAC(细菌人工染色体)标记的 FISH(荧光原位杂交),将糖甜菜的连锁群分配到物理染色体臂上。将糖甜菜的遗传图谱与染色体臂相关联,并建立了连锁群的南北方向。FISH 核型为基因组研究提供了技术平台,可用于编号和鉴定相关野生甜菜物种的染色体。BAC 探针可区分所有九条染色体,使我们能够研究糖甜菜基因组中主要重复成分的染色体特异性分布,包括着丝粒、居间和端粒卫星以及 18S-5.8S-25S 和 5S rRNA 基因簇。我们开发了一种多色 FISH 程序,允许使用卫星 DNA 探针池在单个杂交中鉴定所有九条糖甜菜染色体对。纤维 FISH 用于分析五条染色体臂,其中连锁群的最远端遗传标记被映射到粗线期染色体上的末端重复序列附近。只有在两条臂上,端粒阵列和标记是物理连接的,因此这些连锁群可以被认为是末端封闭的,这使得难以进一步识别远端信息标记。这些结果支持通过标记定位进行遗传作图、用于注释甜菜基因组序列的 contigs 和支架的锚定以及分析主要重复 DNA 家族的染色体分布模式。