Miyao Akio, Tanaka Katsuyuki, Murata Kazumasa, Sawaki Hiromichi, Takeda Shin, Abe Kiyomi, Shinozuka Yoriko, Onosato Katsura, Hirochika Hirohiko
Molecular Genetics Department, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.
Plant Cell. 2003 Aug;15(8):1771-80. doi: 10.1105/tpc.012559.
Because retrotransposons are the major component of plant genomes, analysis of the target site selection of retrotransposons is important for understanding the structure and evolution of plant genomes. Here, we examined the target site specificity of the rice retrotransposon Tos17, which can be activated by tissue culture. We have produced 47,196 Tos17-induced insertion mutants of rice. This mutant population carries approximately 500,000 insertions. We analyzed >42,000 flanking sequences of newly transposed Tos17 copies from 4316 mutant lines. More than 20,000 unique loci were assigned on the rice genomic sequence. Analysis of these sequences showed that insertion events are three times more frequent in genic regions than in intergenic regions. Consistent with this result, Tos17 was shown to prefer gene-dense regions over centromeric heterochromatin regions. Analysis of insertion target sequences revealed a palindromic consensus sequence, ANGTT-TSD-AACNT, flanking the 5-bp target site duplication. Although insertion targets are distributed throughout the chromosomes, they tend to cluster, and 76% of the clusters are located in genic regions. The mechanisms of target site selection by Tos17, the utility of the mutant lines, and the knockout gene database are discussed. --The nucleotide sequence data were uploaded to the DDBJ, EMBL, and GenBank nucleotide sequence databases under accession numbers AG020727 to AG025611 and AG205093 to AG215049.
由于逆转座子是植物基因组的主要组成部分,分析逆转座子的靶位点选择对于理解植物基因组的结构和进化至关重要。在此,我们研究了可通过组织培养激活的水稻逆转座子Tos17的靶位点特异性。我们已产生了47196个由Tos17诱导的水稻插入突变体。这个突变群体携带了约500000个插入。我们分析了来自4316个突变系的新转座的Tos17拷贝的>42000个侧翼序列。在水稻基因组序列上确定了20000多个独特位点。对这些序列的分析表明,插入事件在基因区域的发生频率是基因间区域的三倍。与这一结果一致,Tos17显示出更喜欢基因密集区域而非着丝粒异染色质区域。对插入靶序列的分析揭示了一个回文共有序列ANGTT - TSD - AACNT,位于5个碱基对的靶位点重复两侧。尽管插入靶标分布在整个染色体上,但它们倾向于聚集,并且76%的簇位于基因区域。文中讨论了Tos17选择靶位点的机制、突变体系的效用以及敲除基因数据库。——核苷酸序列数据已上传至DDBJ、EMBL和GenBank核苷酸序列数据库,登录号为AG020727至AG025611以及AG205093至AG215049。