Hwang J E, Kim S-H, Jung I J, Han S M, Ahn J-W, Kwon S-J, Kim S H, Kang S-Y, Kim D S, Kim J-B
Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup, Jeonbuk, Republic of Korea.
Division of Ecological Conservation, Bureau of Ecological Research, National Institute of Ecology, Seocheon, Republic of Korea.
Genet Mol Res. 2016 Dec 23;15(4):gmr-15-04-gmr.15049092. doi: 10.4238/gmr15049092.
Comparative genomic hybridization (CGH) is a powerful tool used to analyze changes in copy number, polymorphisms, and structural variations in the genome. Gene copy number variation (CNV) is a common form of natural diversity in the genome, which can create new genes and alter gene structure. Thus, CNVs may influence phenotypic variation and gene expression. In this study, to detect CNVs, we irradiated rice seeds with gamma rays (300 Gy) and selected two dwarf mutagenized plants, GA-III-189 and -1052, in the M generation. These plants were subjected to CGH analysis using Agilent's RICE CGH array. Most of the CNVs identified were less than 10 kb in length. We detected 90 amplified and 18 deleted regions in GA-III-189, and 99 amplified and 11 deleted regions in GA-III-1052. Of note, CNVs were located on chromosome 12 in both GA-III-189 and -1052, which contained 39 commonly amplified regions in 29 genes. The commonly amplified genes included six genes encoding F-box domain-containing proteins. Alterations in these F-box domain-containing genes were confirmed by quantitative RT-PCR. Integration of CGH and gene expression data identified copy number aberrations and novel genes potentially involved in the dwarf phenotype. These CGH and gene expression data may be useful for uncovering the mechanisms underlying the dwarf phenotype.
比较基因组杂交(CGH)是一种用于分析基因组中拷贝数变化、多态性和结构变异的强大工具。基因拷贝数变异(CNV)是基因组中自然多样性的一种常见形式,它可以产生新基因并改变基因结构。因此,CNV可能影响表型变异和基因表达。在本研究中,为了检测CNV,我们用伽马射线(300 Gy)辐照水稻种子,并在M代中选择了两株矮化诱变植株GA-III-189和-1052。使用安捷伦的水稻CGH芯片对这些植株进行CGH分析。鉴定出的大多数CNV长度小于10 kb。我们在GA-III-189中检测到90个扩增区域和18个缺失区域,在GA-III-1052中检测到99个扩增区域和11个缺失区域。值得注意的是,GA-III-189和-1052中的CNV都位于第12号染色体上,其中包含29个基因中的39个常见扩增区域。常见的扩增基因包括六个编码含F-box结构域蛋白的基因。通过定量RT-PCR证实了这些含F-box结构域基因的改变。CGH和基因表达数据的整合确定了可能与矮化表型有关的拷贝数畸变和新基因。这些CGH和基因表达数据可能有助于揭示矮化表型的潜在机制。