Murata Toshiki, Kadotani Naoki, Yamaguchi Miki, Tosa Yukio, Mayama Shigeyuki, Nakayashiki Hitoshi
Laboratory of Plant Pathology, Graduate School of Agricultural Science, Kobe University, Kobe 657-8501, Japan.
Nucleic Acids Res. 2007;35(18):5987-94. doi: 10.1093/nar/gkm646. Epub 2007 Aug 28.
The LTR-retrotransposon MAGGY was introduced into naive genomes of Magnaporthe oryzae with different genetic backgrounds (wild-type, and MoDcl1 [mdl1] and MoDcl2 [mdl2] dicer mutants). The MoDcl2 mutants deficient in MAGGY siRNA biogenesis generally showed greater MAGGY mRNA accumulation and more rapid increase in MAGGY copy number than did the wild-type and MoDcl1 mutants exhibiting normal MAGGY siRNA accumulation, indicating that RNA silencing functioned as an effective defense against the invading element. Interestingly, however, regardless of genetic background, the rate of MAGGY transposition drastically decreased as its copy number in the genome increased. Notably, in the MoDcl2 mutant, copy-number-dependent MAGGY suppression occurred without a reduction in its mRNA accumulation, and therefore by a silencing mechanism distinct from both transcriptional gene silencing and siRNA-mediated RNA silencing. This might imply that some mechanism possibly similar to post-transcriptional cosuppression of Ty1 retrotransposition in Saccharomyces cerevisiae, which operates regardless of the abundance of target transcript and independent of RNA silencing, would also function in M. oryzae that possesses the RNA silencing machinery.
长末端重复序列反转录转座子MAGGY被导入具有不同遗传背景(野生型、MoDcl1 [mdl1]和MoDcl2 [mdl2]切丁酶突变体)的稻瘟病菌原始基因组中。与表现出正常MAGGY小干扰RNA积累的野生型和MoDcl1突变体相比,缺乏MAGGY小干扰RNA生物合成的MoDcl2突变体通常表现出更高的MAGGY信使核糖核酸积累以及MAGGY拷贝数更快的增加,这表明RNA沉默起到了抵御入侵元件的有效防御作用。然而,有趣的是,无论遗传背景如何,随着MAGGY在基因组中的拷贝数增加,其转座率急剧下降。值得注意的是,在MoDcl2突变体中,拷贝数依赖性的MAGGY抑制发生时,其信使核糖核酸积累并未减少,因此是通过一种不同于转录基因沉默和小干扰RNA介导的RNA沉默的沉默机制。这可能意味着,一些可能类似于酿酒酵母中Ty1反转录转座的转录后共抑制的机制,该机制不依赖于靶转录本的丰度且独立于RNA沉默,在拥有RNA沉默机制的稻瘟病菌中也会发挥作用。