首页> 美国卫生研究院文献>G3: GenesGenomesGenetics >Toward a Molecular Cytogenetic Map for Cultivated Sunflower (Helianthus annuus L.) by Landed BAC/BIBAC Clones
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Toward a Molecular Cytogenetic Map for Cultivated Sunflower (Helianthus annuus L.) by Landed BAC/BIBAC Clones

机译:登陆BAC / BIBAC克隆构建向日葵(Helianthus annuus L.)分子细胞遗传图谱

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摘要

Conventional karyotypes and various genetic linkage maps have been established in sunflower (Helianthus annuus L., 2n = 34). However, the relationship between linkage groups and individual chromosomes of sunflower remains unknown and has considerable relevance for the sunflower research community. Recently, a set of linkage group-specific bacterial /binary bacterial artificial chromosome (BAC/BIBAC) clones was identified from two complementary BAC and BIBAC libraries constructed for cultivated sunflower cv. HA89. In the present study, we used these linkage group-specific clones (∼100 kb in size) as probes to in situ hybridize to HA89 mitotic chromosomes at metaphase using the BAC- fluorescence in situ hybridization (FISH) technique. Because a characteristic of the sunflower genome is the abundance of repetitive DNA sequences, a high ratio of blocking DNA to probe DNA was applied to hybridization reactions to minimize the background noise. As a result, all sunflower chromosomes were anchored by one or two BAC/BIBAC clones with specific FISH signals. FISH analysis based on tandem repetitive sequences, such as rRNA genes, has been previously reported; however, the BAC-FISH technique developed here using restriction fragment length polymorphism (RFLP)−derived BAC/BIBAC clones as probes to apply genome-wide analysis is new for sunflower. As chromosome-specific cytogenetic markers, the selected BAC/BIBAC clones that encompass the 17 linkage groups provide a valuable tool for identifying sunflower cytogenetic stocks (such as trisomics) and tracking alien chromosomes in interspecific crosses. This work also demonstrates the potential of using a large-insert DNA library for the development of molecular cytogenetic resources.
机译:在向日葵中已经建立了常规的核型和各种遗传连锁图谱(Helianthus annuus L.,2n = 34)。然而,连接基团与向日葵个体染色体之间的关系仍然未知,并且对向日葵研究界具有重要意义。最近,从构建用于培养向日葵cv的两个互补BAC和BIBAC库中鉴定出一组特定于连锁基团的细菌/二进制细菌人工染色体(BAC / BIBAC)克隆。 HA89。在本研究中,我们使用这些连锁基团特异性克隆(大小约为100 kb)作为探针,使用BAC-荧光原位杂交(FISH)技术在中期将其与HA89有丝分裂染色体原位杂交。由于向日葵基因组的特征是重复DNA序列的丰度,因此将高比例的封闭DNA与探针DNA应用于杂交反应,以将背景噪音降至最低。结果,所有向日葵染色体都被一个或两个具有特定FISH信号的BAC / BIBAC克隆锚定。以前曾报道过基于串联重复序列(如rRNA基因)的FISH分析;但是,这里开发的BAC-FISH技术使用了限制性片段长度多态性(RFLP)衍生的BAC / BIBAC克隆作为探针,可以进行全基因组分析,这对于向日葵来说是新的。作为染色体特异的细胞遗传标记,选定的BAC / BIBAC克隆包含17个连接基团,为鉴定向日葵的细胞遗传种群(例如三体组)和跟踪种间杂交中的外来染色体提供了宝贵的工具。这项工作还证明了使用大插入DNA库开发分子细胞遗传资源的潜力。

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