Hirochika H, Sugimoto K, Otsuki Y, Tsugawa H, Kanda M
Department of Molecular Biology, National Institute of Agrobiological Resources, Tsukuba, Japan.
Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7783-8. doi: 10.1073/pnas.93.15.7783.
Five retrotransposon families of rice (Tos1-Tos5) have been reported previously. Here we report 15 new retrotransposon families of rice (Tos6-Tos20). In contrast to yeast and Drosophila retrotransposons, all of the rice retrotransposons examined appear inactive (or almost inactive) under normal growth conditions. Three of the rice retrotransposons (Tos10, Tos17, and Tos19) are activated under tissue culture conditions. The most active one, Tos17, was studied in detail. The copy number of Tos17 increased with prolonged culture period. In all of the plants regenerated from tissue cultures, including transgenic plants, 5 to 30 transposed Tos17 copies were detected. The transcript of Tos17 was only detected under tissue culture conditions, indicating that the transposition of Tos17 is mainly regulated at the transcriptional level. To examine the target-site specificity of Tos17 transposition, sequences flanking transposed Tos17 copies were analyzed. At least four out of eight target sites examined are coding regions. Other target sites may also be in genes because two out of four were transcribed. The regenerated plants with Tos17-insertions in the phytochrome A gene and the S-receptor kinase-related gene were identified. These results indicate that activation of Tos17 is an important cause of tissue culture-induced mutations. Tissue culture-induced activation of Tos17 may be a useful tool for insertional mutagenesis and functional analysis of genes.
此前已报道了水稻的五个反转录转座子家族(Tos1 - Tos5)。在此我们报道水稻的15个新反转录转座子家族(Tos6 - Tos20)。与酵母和果蝇的反转录转座子不同,所检测的所有水稻反转录转座子在正常生长条件下似乎都无活性(或几乎无活性)。其中三个水稻反转录转座子(Tos10、Tos17和Tos19)在组织培养条件下被激活。对最活跃的Tos17进行了详细研究。Tos17的拷贝数随着培养时间的延长而增加。在所有从组织培养再生的植株中,包括转基因植株,检测到5至30个发生转座的Tos17拷贝。Tos17的转录本仅在组织培养条件下被检测到,这表明Tos17的转座主要在转录水平受到调控。为了检测Tos17转座的靶位点特异性,对发生转座的Tos17拷贝两侧的序列进行了分析。在所检测的八个靶位点中,至少有四个是编码区。其他靶位点可能也在基因中,因为四个中有两个被转录了。鉴定出了在光敏色素A基因和S受体激酶相关基因中插入Tos17的再生植株。这些结果表明Tos17的激活是组织培养诱导突变的一个重要原因。组织培养诱导的Tos17激活可能是用于插入诱变和基因功能分析的一个有用工具。