Arikit Siwaret, Xia Rui, Kakrana Atul, Huang Kun, Zhai Jixian, Yan Zhe, Valdés-López Oswaldo, Prince Silvas, Musket Theresa A, Nguyen Henry T, Stacey Gary, Meyers Blake C
Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19711 Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711.
Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711.
Plant Cell. 2014 Dec;26(12):4584-601. doi: 10.1105/tpc.114.131847. Epub 2014 Dec 2.
Small RNAs are ubiquitous, versatile repressors and include (1) microRNAs (miRNAs), processed from mRNA forming stem-loops; and (2) small interfering RNAs (siRNAs), the latter derived in plants by a process typically requiring an RNA-dependent RNA polymerase. We constructed and analyzed an expression atlas of soybean (Glycine max) small RNAs, identifying over 500 loci generating 21-nucleotide phased siRNAs (phasiRNAs; from PHAS loci), of which 483 overlapped annotated protein-coding genes. Via the integration of miRNAs with parallel analysis of RNA end (PARE) data, 20 miRNA triggers of 127 PHAS loci were detected. The primary class of PHAS loci (208 or 41% of the total) corresponded to NB-LRR genes; some of these small RNAs preferentially accumulate in nodules. Among the PHAS loci, novel representatives of TAS3 and noncanonical phasing patterns were also observed. A noncoding PHAS locus, triggered by miR4392, accumulated preferentially in anthers; the phasiRNAs are predicted to target transposable elements, with their peak abundance during soybean reproductive development. Thus, phasiRNAs show tremendous diversity in dicots. We identified novel miRNAs and assessed the veracity of soybean miRNAs registered in miRBase, substantially improving the soybean miRNA annotation, facilitating an improvement of miRBase annotations and identifying at high stringency novel miRNAs and their targets.
小RNA广泛存在且功能多样,包括:(1)从形成茎环的mRNA加工而来的微小RNA(miRNA);(2)小干扰RNA(siRNA),后者在植物中通过通常需要RNA依赖的RNA聚合酶的过程产生。我们构建并分析了大豆(Glycine max)小RNA的表达图谱,鉴定出500多个产生21个核苷酸相位siRNA(phasiRNA;来自PHAS位点)的位点,其中483个与注释的蛋白质编码基因重叠。通过将miRNA与RNA末端平行分析(PARE)数据整合,检测到127个PHAS位点的20个miRNA触发因子。主要的PHAS位点类别(占总数的208个或41%)对应于NB-LRR基因;其中一些小RNA优先在根瘤中积累。在PHAS位点中,还观察到了TAS3的新代表和非经典相位模式。一个由miR4392触发的非编码PHAS位点优先在花药中积累;预测这些phasiRNA靶向转座元件,其丰度在大豆生殖发育期间达到峰值。因此,phasiRNA在双子叶植物中表现出极大的多样性。我们鉴定了新的miRNA,并评估了miRBase中注册的大豆miRNA的准确性,大幅改进了大豆miRNA注释,有助于改进miRBase注释,并以高严格度鉴定新的miRNA及其靶标。