Lu Cheng, Kulkarni Karthik, Souret Frédéric F, MuthuValliappan Ramesh, Tej Shivakundan Singh, Poethig R Scott, Henderson Ian R, Jacobsen Steven E, Wang Wenzhong, Green Pamela J, Meyers Blake C
Department of Plant and Soil Sciences & Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711, USA;
Genome Res. 2006 Oct;16(10):1276-88. doi: 10.1101/gr.5530106. Epub 2006 Sep 5.
The Arabidopsis genome contains a highly complex and abundant population of small RNAs, and many of the endogenous siRNAs are dependent on RNA-Dependent RNA Polymerase 2 (RDR2) for their biogenesis. By analyzing an rdr2 loss-of-function mutant using two different parallel sequencing technologies, MPSS and 454, we characterized the complement of miRNAs expressed in Arabidopsis inflorescence to considerable depth. Nearly all known miRNAs were enriched in this mutant and we identified 13 new miRNAs, all of which were relatively low abundance and constitute new families. Trans-acting siRNAs (ta-siRNAs) were even more highly enriched. Computational and gel blot analyses suggested that the minimal number of miRNAs in Arabidopsis is approximately 155. The size profile of small RNAs in rdr2 reflected enrichment of 21-nt miRNAs and other classes of siRNAs like ta-siRNAs, and a significant reduction in 24-nt heterochromatic siRNAs. Other classes of small RNAs were found to be RDR2-independent, particularly those derived from long inverted repeats and a subset of tandem repeats. The small RNA populations in other Arabidopsis small RNA biogenesis mutants were also examined; a dcl2/3/4 triple mutant showed a similar pattern to rdr2, whereas dcl1-7 and rdr6 showed reductions in miRNAs and ta-siRNAs consistent with their activities in the biogenesis of these types of small RNAs. Deep sequencing of mutants provides a genetic approach for the dissection and characterization of diverse small RNA populations and the identification of low abundance miRNAs.
拟南芥基因组包含高度复杂且丰富的小RNA群体,许多内源性小干扰RNA(siRNA)的生物合成依赖于RNA依赖的RNA聚合酶2(RDR2)。通过使用两种不同的平行测序技术MPSS和454分析rdr2功能缺失突变体,我们相当深入地描绘了拟南芥花序中表达的微小RNA(miRNA)的互补情况。几乎所有已知的miRNA在该突变体中都得到了富集,并且我们鉴定出13个新的miRNA,它们均丰度相对较低,构成了新的家族。反式作用小干扰RNA(ta-siRNA)的富集程度甚至更高。计算分析和凝胶印迹分析表明,拟南芥中miRNA的最小数量约为155个。rdr2中小RNA的大小分布反映出21核苷酸miRNA和其他类型的siRNA如ta-siRNA的富集,以及24核苷酸异染色质siRNA的显著减少。发现其他类型的小RNA不依赖RDR2,特别是那些源自长反向重复序列和串联重复序列子集的小RNA。我们还检测了拟南芥其他小RNA生物合成突变体中的小RNA群体;dcl2/3/4三突变体显示出与rdr2相似的模式,而dcl1-7和rdr6中miRNA和ta-siRNA减少情况与它们在这些类型小RNA生物合成中的作用一致。对突变体进行深度测序为剖析和表征多样的小RNA群体以及鉴定低丰度miRNA提供了一种遗传学方法。