Jiang J, Gill B S, Wang G L, Ronald P C, Ward D C
Department of Plant Pathology, Kansas State University, Manhattan 66506-5502, USA.
Proc Natl Acad Sci U S A. 1995 May 9;92(10):4487-91. doi: 10.1073/pnas.92.10.4487.
Fluorescence in situ hybridization (FISH) is a powerful tool for physical mapping in human and other mammalian species. However, application of the FISH technique has been limited in plant species, especially for mapping single- or low-copy DNA sequences, due to inconsistent signal production in plant chromosome preparations. Here we demonstrate that bacterial artificial chromosome (BAC) clones can be mapped readily on rice (Oryza sativa L.) chromosomes by FISH. Repetitive DNA sequences in BAC clones can be suppressed efficiently by using rice genomic DNA as a competitor in the hybridization mixture. BAC clones as small as 40 kb were successfully mapped. To demonstrate the application of the FISH technique in physical mapping of plant genomes, both anonymous BAC clones and clones closely linked to a rice bacterial blight-resistance locus, Xa21, were chosen for analysis. The physical location of Xa21 and the relationships among the linked clones were established, thus demonstrating the utility of FISH in plant genome analysis.
荧光原位杂交(FISH)是在人类和其他哺乳动物物种中进行物理图谱绘制的强大工具。然而,由于植物染色体标本中信号产生不一致,FISH技术在植物物种中的应用受到限制,特别是在绘制单拷贝或低拷贝DNA序列时。在此,我们证明细菌人工染色体(BAC)克隆可通过FISH轻松定位到水稻(Oryza sativa L.)染色体上。在杂交混合物中使用水稻基因组DNA作为竞争者,可以有效抑制BAC克隆中的重复DNA序列。小至40 kb的BAC克隆已成功定位。为了证明FISH技术在植物基因组物理图谱绘制中的应用,我们选择了匿名BAC克隆和与水稻白叶枯病抗性基因座Xa21紧密连锁的克隆进行分析。确定了Xa21的物理位置以及连锁克隆之间的关系,从而证明了FISH在植物基因组分析中的实用性。