Hayashi-Tsugane Mika, Maekawa Masahiko, Tsugane Kazuo
National Institute for Basic Biology, Okazaki 444-8585, Japan.
Institute of Plant Science and Resources, Okayama University, Kurashiki 710-0046, Japan.
Sci Rep. 2015 Sep 25;5:14357. doi: 10.1038/srep14357.
A non-autonomous DNA transposon in rice, nDart1, is actively transposed in the presence of an autonomous element, aDart1, under natural conditions. The nDart1-promoted gene tagging line was developed using the endogenous nDart1/aDart1 system to generate various rice mutants effectively. While the dominant mutants were occasionally isolated from the tagging line, it was unclear what causes dominant mutations. A semidominant mutant, Bushy dwarf tiller1 (Bdt1), which has the valuable agronomic traits of multiple tillering and dwarfism, was obtained from the tagging line. Bdt1 mutant carried a newly inserted nDart1 at 38-bp upstream of transcription initiation site of a non-protein-coding gene, miR156d. This insertion caused an upstream shift of the miR156d transcription initiation site and, consequently, increased the functional transcripts producing mature microRNAs. These results indicate that the total amount of miR156d is controlled not only by transcript quantity but also by transcript quality. Furthermore, transgenic lines introduced an miR156d fragment that flanked the nDart1 sequence at the 5' region, suggesting that insertion of nDart1 in the gene promoter region enhances gene expression as a cis-element. This study demonstrates the ability of nDart1 to produce gain-of-function mutants as well as further insights into the function of transposable elements in genome evolution.
水稻中的一个非自主DNA转座子nDart1,在自然条件下,于自主元件aDart1存在时会发生活跃转座。利用内源性nDart1/aDart1系统开发了nDart1促进的基因标签系,以有效产生各种水稻突变体。虽然偶尔会从标签系中分离出显性突变体,但不清楚导致显性突变的原因。从标签系中获得了一个半显性突变体,丛生矮化分蘖1(Bdt1),它具有多分蘖和矮化的宝贵农艺性状。Bdt1突变体在一个非蛋白质编码基因miR156d转录起始位点上游38bp处携带一个新插入的nDart1。这种插入导致miR156d转录起始位点向上游移动,从而增加了产生成熟微小RNA的功能性转录本。这些结果表明,miR156d的总量不仅受转录本数量控制,还受转录本质量控制。此外,转基因系在5'区域引入了一个位于nDart1序列侧翼的miR156d片段,这表明nDart1插入基因启动子区域可作为顺式元件增强基因表达。本研究证明了nDart1产生功能获得性突变体的能力,以及对转座元件在基因组进化中功能的进一步深入了解。