Raizada M N, Nan G L, Walbot V
Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USA.
Plant Cell. 2001 Jul;13(7):1587-608. doi: 10.1105/tpc.010002.
RescueMu, a Mu1 element containing a bacterial plasmid, is mobilized by MuDR in transgenic maize. Somatic excision from a cell-autonomous marker gene yields >90% single cell sectors; empty donor sites often have deletions and insertions, including up to 210 bp of RescueMu/Mu1 terminal DNA. Late somatic insertions are contemporaneous with excisions, suggesting that "cut-and-paste" transposition occurs in the soma. During reproduction, RescueMu transposes infrequently from the initial transgene array, but once transposed, RescueMu is suitable for high throughput gene mutation and cloning. As with MuDR/Mu elements, heritable RescueMu insertions are not associated with excisions. Both somatic and germinal RescueMu insertions occur preferentially into genes and gene-like sequences, but they exhibit weak target site preferences. New insights into Mu behaviors are discussed with reference to two models proposed to explain the alternative outcomes of somatic and germinal events: a switch from somatic cut-and-paste to germinal replicative transposition or to host-mediated gap repair from sister chromatids.
RescueMu是一种含有细菌质粒的Mu1元件,在转基因玉米中由MuDR激活。从细胞自主标记基因进行体细胞切除可产生超过90%的单细胞扇形区;空的供体位点常有缺失和插入,包括长达210 bp的RescueMu/Mu1末端DNA。晚期体细胞插入与切除同时发生,这表明“剪切粘贴”转座发生在体细胞中。在繁殖过程中,RescueMu很少从初始转基因阵列中转座,但一旦转座,RescueMu就适用于高通量基因突变和克隆。与MuDR/Mu元件一样,可遗传的RescueMu插入与切除无关。体细胞和生殖细胞中的RescueMu插入都优先发生在基因和类基因序列中,但它们表现出较弱的靶位点偏好性。参照提出的两种模型讨论了对Mu行为的新见解,这两种模型用于解释体细胞和生殖细胞事件的不同结果:从体细胞的“剪切粘贴”转座转变为生殖细胞的复制性转座,或转变为宿主介导的姐妹染色单体间隙修复。