Takumi Shigeo, Walbot Virginia
Department of Biological Sciences, Stanford University, CA 94305-5020, USA.
Genes Genet Syst. 2007 Oct;82(5):387-401. doi: 10.1266/ggs.82.387.
Maize MuDR/Mu elements are one of the most active Class II transposons and are widely used for transposon tagging for gene cloning. The autonomous MuDR encodes a transposase, while diverse non-autonomous elements share similarity to MuDR only within their ~215 bp terminal inverted repeats (TIRs). Four independent Mu-induced mutable alleles of the anthocyanin pigment pathway Bronze2 (Bz2) locus have been sequenced; bz2-mu1, bz2-mu2, and bz2-mu3 contain Mu1 element insertions while bz2-mu4 contains a MuDR insertion. Somatic excision activity can be monitored for each allele as a purple spotted phenotype on the otherwise beige epidermal layer of the kernel. To study epigenetic silencing of Mu elements, we investigated inheritance of somatic transposition of these four reporter alleles, and using samples from leaves just below the ear and the tassel, DNA methylation status and mudrA expression were quantified through three consecutive generations. Percentages of spotted kernels when crossed into bz2 tester as pollen parent were lower than those when crossed with bz2 tester as ear parent in all bz2-mu alleles. The propensity for silencing in kernels with different frequencies of spotting was investigated. In the inactive lines, both MuDR and Mu1 elements were de novo methylated. The transposition frequency was negatively correlated with the level of Mu methylation and positively correlated with the level of mudrA transcript. The most reliable indicator of incipient silencing was a decrease in mudrA transcript levels in the leaf below the tassel, and this transcriptional silencing could precede methylation of Mu elements.
玉米MuDR/Mu元件是最活跃的II类转座子之一,被广泛用于基因克隆的转座子标签技术。自主型MuDR编码一种转座酶,而多种非自主型元件仅在其约215 bp的末端反向重复序列(TIRs)内与MuDR具有相似性。已对花青素色素途径Bronze2(Bz2)位点的四个独立的Mu诱导的可变等位基因进行了测序;bz2-mu1、bz2-mu2和bz2-mu3含有Mu1元件插入,而bz2-mu4含有一个MuDR插入。每个等位基因的体细胞切除活性可通过籽粒原本米色的表皮层上的紫色斑点表型来监测。为了研究Mu元件的表观遗传沉默,我们调查了这四个报告等位基因的体细胞转座的遗传情况,并使用穗下方和雄穗下方叶片的样本,连续三代对DNA甲基化状态和mudrA表达进行了定量分析。当作为花粉亲本与bz2测试系杂交时,有斑点籽粒的百分比低于作为母本与bz2测试系杂交时的百分比。研究了不同斑点频率的籽粒中沉默的倾向。在无活性系中,MuDR和Mu1元件均发生了从头甲基化。转座频率与Mu甲基化水平呈负相关,与mudrA转录本水平呈正相关。初始沉默最可靠的指标是雄穗下方叶片中mudrA转录本水平的降低,这种转录沉默可能先于Mu元件的甲基化。