Tsugane Kazuo, Maekawa Masahiko, Takagi Kyoko, Takahara Hiroyuki, Qian Qian, Eun Chang-Ho, Iida Shigeru
National Institute for Basic Biology, Okazaki 444-8585, Japan.
Plant J. 2006 Jan;45(1):46-57. doi: 10.1111/j.1365-313X.2005.02600.x.
While characterized mutable alleles caused by DNA transposons have been abundant in maize since the discovery of Dissociation conferring variegation by Barbara McClintock, only a few mutable alleles have been described in rice even though the rice genome contains various transposons. Here, we show that a spontaneous mutable virescent allele, pyl-v, is caused by the disruption of the nuclear-coded essential chloroplast protease gene, OsClpP5, due to insertion of a 607-bp non-autonomous DNA transposon, non-autonomous DNA-based active rice transposon one (nDart1), belonging to the hAT superfamily. The transposition of nDart1 can be induced by crossing with a line containing an autonomous element, aDart, and stabilized by segregating out of aDart. We also identified a novel mutable dwarf allele thl-m caused by an insertion of nDart1. The japonica cultivar Nipponbare carries no aDart, although it contains epigenetically silenced Dart element(s), which can be activated by 5-azacytidine. Nipponbare bears four subgroups of about 3.6-kb Dart-like sequences, three of which contain potential transposase genes, and around 3.6-kb elements without an apparent transposase gene, as well as three subgroups of about 0.6-kb nDart1-related elements that are all internal deletions of the Dart-like sequences. Both nDart1 and 3.6-kb Dart-like elements were also present in indica varieties 93-11 and Kasalath. nDart1 appears to be the most active mutagen among nDart1-related elements contributing to generating natural variations. A candidate for an autonomous element, aDart, and a possible application of nDart1 for transposon tagging are discussed.
自芭芭拉·麦克林托克发现解离基因导致玉米出现斑驳现象以来,由DNA转座子引起的具有特征性的可变等位基因在玉米中大量存在。尽管水稻基因组中含有各种转座子,但在水稻中仅描述了少数可变等位基因。在此,我们表明,一个自发的可变绿色减退等位基因pyl-v是由于一个607碱基对的非自主DNA转座子——属于hAT超家族的基于非自主DNA的活性水稻转座子1(nDart1)插入,破坏了核编码的叶绿体必需蛋白酶基因OsClpP5所致。nDart1的转座可通过与含有自主元件aDart的品系杂交诱导产生,并通过分离出aDart而稳定下来。我们还鉴定出一个由nDart1插入引起的新型可变矮化等位基因thl-m。粳稻品种日本晴虽然含有表观遗传沉默的Dart元件,但不携带aDart,这些元件可被5-氮杂胞苷激活。日本晴带有约3.6千碱基对的Dart样序列的四个亚组,其中三个含有潜在的转座酶基因,还有约3.6千碱基对没有明显转座酶基因的元件,以及约0.6千碱基对的nDart1相关元件的三个亚组,它们都是Dart样序列的内部缺失。nDart1和3.6千碱基对的Dart样元件也存在于籼稻品种93-11和卡萨拉斯中。nDart1似乎是nDart1相关元件中最活跃的诱变剂,有助于产生自然变异。文中讨论了自主元件aDart的候选者以及nDart1在转座子标签中的可能应用。