Fuji Kentaro, Shimada Tomoo, Takahashi Hideyuki, Tamura Kentaro, Koumoto Yasuko, Utsumi Shigeru, Nishizawa Keito, Maruyama Nobuyuki, Hara-Nishimura Ikuko
Department of Botany, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
Plant Cell. 2007 Feb;19(2):597-609. doi: 10.1105/tpc.106.045997. Epub 2007 Feb 9.
Two Arabidopsis thaliana genes have been shown to function in vacuolar sorting of seed storage proteins: a vacuolar sorting receptor, VSR1/ATELP1, and a retromer component, MAIGO1 (MAG1)/VPS29. Here, we show an efficient and simple method for isolating vacuolar sorting mutants of Arabidopsis. The method was based on two findings in this study. First, VSR1 functioned as a sorting receptor for beta-conglycinin by recognizing the vacuolar targeting signal. Second, when green fluorescent protein (GFP) fusion with the signal (GFP-CT24) was expressed in vsr1, mag1/vps29, and wild-type seeds, both vsr1and mag1/vps29 gave strongly fluorescent seeds but the wild type did not, suggesting that a defect in vacuolar sorting provided fluorescent seeds by the secretion of GFP-CT24 out of the cells. We mutagenized transformant seeds expressing GFP-CT24. From approximately 3,000,000 lines of M2 seeds, we obtained >100 fluorescent seeds and designated them green fluorescent seed (gfs) mutants. We report 10 gfs mutants, all of which caused missorting of storage proteins. We mapped gfs1 to VSR1, gfs2 to KAM2/GRV2, gfs10 to the At4g35870 gene encoding a novel membrane protein, and the others to different loci. This method should provide valuable insights into the complex molecular mechanisms underlying vacuolar sorting of storage proteins.
一个液泡分选受体VSR1/ATELP1和一个回收蛋白复合物组分MAIGO1 (MAG1)/VPS29。在此,我们展示了一种高效且简单的分离拟南芥液泡分选突变体的方法。该方法基于本研究中的两个发现。第一,VSR1通过识别液泡靶向信号,作为β-伴大豆球蛋白的分选受体发挥作用。第二,当绿色荧光蛋白(GFP)与该信号(GFP-CT24)的融合蛋白在vsr1、mag1/vps29和野生型种子中表达时,vsr1和mag1/vps29产生强荧光种子,而野生型则不产生,这表明液泡分选缺陷会通过GFP-CT24分泌到细胞外而产生荧光种子。我们对表达GFP-CT24的转化体种子进行诱变处理。从大约300万株M2种子中,我们获得了100多个荧光种子,并将它们命名为绿色荧光种子(gfs)突变体。我们报道了10个gfs突变体,所有这些突变体都会导致储存蛋白分选错误。我们将gfs1定位到VSR1,gfs2定位到KAM2/GRV2,gfs10定位到编码一种新型膜蛋白的At4g35870基因,其他突变体则定位到不同的位点。该方法应该能为储存蛋白液泡分选背后复杂的分子机制提供有价值的见解。