Wu Feijie, Yu Lin, Cao Wenguang, Mao Yanfei, Liu Zhongyuan, He Yuke
National Key Laboratory of Plant Molecular Genetics, Shanghai Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.
Plant Cell. 2007 Mar;19(3):914-25. doi: 10.1105/tpc.106.048637. Epub 2007 Mar 2.
Arabidopsis thaliana HYPONASTIC LEAVES1 (HYL1) is a microRNA (miRNA) biogenesis protein that contains two N-terminal double-stranded RNA binding domains (dsRBDs), a putative nuclear localization site (NLS), and a putative protein-protein interaction domain. The interaction of HYL1 with DICER-LIKE1 is important for the efficient and precise processing of miRNA primary transcripts in plant miRNA biogenesis. To define the roles of the various domains of HYL1 in miRNA processing and the miRNA-directed phenotype, we transferred a series of HYL1 deletion constructs into hyl1 null mutants. The N-terminal region containing dsRBD1 and dsRBD2 completely rescued the mutant phenotype of hyl1, triggering the accumulation of miR166 and miR160 and resulting in reduced mRNA levels of the targeted genes. In vivo biochemical analysis of the HYL1-containing complexes from the transgenic plants revealed that the N-terminal dsRBDs of HYL1 were sufficient for processing miRNA precursors and the generation of mature miRNA. Transient and stable expression analysis demonstrated that the putative NLS domain was indeed the nuclear localization signal, whereas the N-terminal region containing the dsRBDs was not restricted to the nucleus. We suggest that the N-terminal dsRBDs fulfill the function of the whole HYL1 and thus play an essential role in miRNA processing and miRNA-directed silencing of targeted genes.
拟南芥叶下卷曲1(HYL1)是一种微小RNA(miRNA)生物合成蛋白,包含两个N端双链RNA结合结构域(dsRBD)、一个假定的核定位位点(NLS)和一个假定的蛋白质-蛋白质相互作用结构域。在植物miRNA生物合成过程中,HYL1与Dicer样蛋白1(DICER-LIKE1)的相互作用对于miRNA初级转录本的高效精确加工至关重要。为了确定HYL1各个结构域在miRNA加工及miRNA介导的表型中的作用,我们将一系列HYL1缺失构建体转入hyl1缺失突变体中。包含dsRBD1和dsRBD2的N端区域完全拯救了hyl1的突变表型,促使miR166和miR160积累,并导致靶基因的mRNA水平降低。对转基因植物中含HYL1复合物的体内生化分析表明,HYL1的N端dsRBD足以加工miRNA前体并产生成熟的miRNA。瞬时和稳定表达分析表明,假定的NLS结构域确实是核定位信号,而包含dsRBD的N端区域并不局限于细胞核。我们认为,N端dsRBD发挥了整个HYL1的功能,因此在miRNA加工及miRNA介导的靶基因沉默中起关键作用。