Huang Jian, Zhang Kewei, Shen Yi, Huang Zejun, Li Ming, Tang Ding, Gu Minghong, Cheng Zhukuan
State Key Laboratory of Plant Genomics and Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Genomics. 2009 Mar;93(3):274-81. doi: 10.1016/j.ygeno.2008.11.007. Epub 2008 Dec 23.
Recent completion of rice genome sequencing has revealed that more than 40% of its genome consists of repetitive sequences, and most of them are related to inactive transposable elements. In the present study, a transposable element, nDaiZ0, which is induced by tissue culture with high frequency, was identified by sequence analysis of an allelic line of the golden hull and internode 2 (gh2) mutant, which was integrated into the forth exon of GH2. The 528-bp nDaiZ0 has 14-bp terminal inverted repeats (TIRs), and generates an 8-bp duplication of its target sites (TSD) during its mobilization. nDaiZs are non-autonomous transposons and have no coding capacity. Bioinformatics analysis and southern blot hybridization showed that at least 16 copies of nDaiZ elements exist in the japonica cultivar Nipponbare genome and 11 copies in the indica cultivar 93-11 genome. During tissue culture, only one copy, nDaiZ9, located on chromosome 5 in the genome of Nipponbare can be activated with its transposable frequency reaching 30%. However, nDaiZ9 was not present in the 93-11 genome. The larger elements, DaiZs, were further identified by database searching using nDaiZ0 as a query because they share similar TIRs and subterminal sequences. DaiZ can also generate an 8-bp TSD. DaiZ elements contain a conserved region with a high similarity to the hAT dimerization motif, suggesting that the nDaiZ-DaiZ transposon system probably belongs to the hAT superfamily of class II transposons. Phylogenetic analysis indicated that it is a new type of plant hAT-like transposon. Although nDaiZ is activated by tissue culture, the high transposable frequency indicates that it could become a useful gene tagging system for rice functional genomic studies. In addition, the mechanism of the high transposable ability of nDaiZ9 is discussed.
最近完成的水稻基因组测序显示,其基因组超过40%由重复序列组成,其中大部分与无活性的转座元件有关。在本研究中,通过对金色颖壳和节间2(gh2)突变体等位系的序列分析,鉴定出一种高频组织培养诱导的转座元件nDaiZ0,它整合到了GH2的第四外显子中。528 bp的nDaiZ0具有14 bp的末端反向重复序列(TIR),并在其转座过程中产生8 bp的靶位点重复序列(TSD)。nDaiZs是非自主转座子,没有编码能力。生物信息学分析和Southern杂交表明,粳稻品种日本晴基因组中至少存在16个nDaiZ元件拷贝,籼稻品种93-11基因组中存在11个拷贝。在组织培养过程中,日本晴基因组中位于第5号染色体上的唯一一个拷贝nDaiZ9能够被激活,其转座频率达到30%。然而,93-11基因组中不存在nDaiZ9。通过以nDaiZ0为查询序列在数据库中搜索,进一步鉴定出了更大的元件DaiZs,因为它们具有相似的TIR和亚末端序列。DaiZ也能产生8 bp的TSD。DaiZ元件包含一个与hAT二聚化基序高度相似的保守区域,这表明nDaiZ-DaiZ转座子系统可能属于II类转座子的hAT超家族。系统发育分析表明它是一种新型的植物类hAT转座子。虽然nDaiZ是由组织培养激活的,但其高转座频率表明它可能成为水稻功能基因组学研究中一种有用的基因标签系统。此外,还讨论了nDaiZ9高转座能力的机制。