伽玛辐照诱导水稻矮化突变体的比较基因组杂交分析。

J. Hwang, S. Kim, I. Jung, S. Han, J-W Ahn, S.-J. Kwon, S. H. Kim, S.-Y. Kang, D. S. Kim, J. Kim
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引用次数: 4

摘要

比较基因组杂交(CGH)是一种用于分析基因组拷贝数、多态性和结构变异变化的强大工具。基因拷贝数变异(CNV)是基因组自然多样性的一种常见形式,它可以产生新的基因和改变基因结构。因此,CNVs可能影响表型变异和基因表达。在本研究中,为了检测CNVs,我们用300 Gy的伽马射线照射水稻种子,选择了M3代的两个矮化诱变植株GA-III-189和-1052。这些植物使用安捷伦的RICE CGH阵列进行CGH分析。大多数克隆变异的长度小于10kb。在GA-III-189中检测到90个扩增区和18个缺失区,在GA-III-1052中检测到99个扩增区和11个缺失区。值得注意的是,GA-III-189和ga -1052的CNVs都位于12号染色体上,包含29个基因的39个常见扩增区域。常见扩增基因包括6个编码含F-box结构域蛋白的基因。这些含F-box结构域基因的改变被定量RT-PCR证实。整合CGH和基因表达数据鉴定拷贝数畸变和新基因可能参与矮化表型。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative genomic hybridization analysis of rice dwarf mutants induced by gamma irradiation.
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 M3 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.
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