Dukowic-Schulze Stefanie, Sundararajan Anitha, Ramaraj Thiruvarangan, Kianian Shahryar, Pawlowski Wojciech P, Mudge Joann, Chen Changbin
Department of Horticultural Science, University of Minnesota, St. Paul MN, USA.
National Center for Genome Resources, Santa Fe NM, USA.
Front Plant Sci. 2016 Jun 2;7:762. doi: 10.3389/fpls.2016.00762. eCollection 2016.
Small RNAs (sRNA) add additional layers to the regulation of gene expression, with siRNAs directing gene silencing at the DNA level by RdDM (RNA-directed DNA methylation), and micro RNAs (miRNAs) directing post-transcriptional regulation of specific target genes, mostly by mRNA cleavage. We used manually isolated male meiocytes from maize (Zea mays) to investigate sRNA and DNA methylation landscapes during zygotene, an early stage of meiosis during which steps of meiotic recombination and synapsis of paired homologous chromosomes take place. We discovered two novel miRNAs from meiocytes, zma-MIR11969 and zma-MIR11970, and identified putative target genes. Furthermore, we detected abundant phasiRNAs of 21 and 24 nt length. PhasiRNAs are phased small RNAs which occur in 21 or 24 nt intervals, at a few hundred loci, specifically in male reproductive tissues in grasses. So far, the function of phasiRNAs remained elusive. Data from isolated meiocytes now revealed elevated DNA methylation at phasiRNA loci, especially in the CHH context, suggesting a role for phasiRNAs in cis DNA methylation. In addition, we consider a role of these phasiRNAs in chromatin remodeling/dynamics during meiosis. However, this is not well supported yet and will need more additional data. Here, we only lay out the idea due to other relevant literature and our additional observation of a peculiar GC content pattern at phasiRNA loci. Chromatin remodeling is also indicated by the discovery that histone genes were enriched for sRNA of 22 nt length. Taken together, we gained clues that lead us to hypothesize sRNA-driven DNA methylation and possibly chromatin remodeling during male meiosis in the monocot maize which is in line with and extends previous knowledge.
小RNA(sRNA)为基因表达调控增添了更多层次,其中小干扰RNA(siRNA)通过RNA介导的DNA甲基化(RdDM)在DNA水平指导基因沉默,而微小RNA(miRNA)主要通过mRNA切割指导特定靶基因的转录后调控。我们使用从玉米(Zea mays)中手动分离的雄配子细胞来研究偶线期(减数分裂的早期阶段,在此期间发生减数分裂重组和配对同源染色体的联会)的sRNA和DNA甲基化图谱。我们从雄配子细胞中发现了两个新的miRNA,即zma - MIR11969和zma - MIR11970,并鉴定了推定的靶基因。此外,我们检测到大量长度为21和24个核苷酸的相位小RNA(phasiRNA)。PhasiRNA是相位小RNA,以21或24个核苷酸的间隔出现,存在于几百个位点,特别是在禾本科植物的雄性生殖组织中。到目前为止,PhasiRNA的功能仍然不清楚。来自分离的雄配子细胞的数据现在显示,在phasiRNA位点的DNA甲基化升高,特别是在CHH背景下,这表明phasiRNA在顺式DNA甲基化中发挥作用。此外,我们认为这些phasiRNA在减数分裂过程中的染色质重塑/动态变化中发挥作用。然而,这一点目前还没有得到充分的支持,还需要更多的数据。在这里,由于其他相关文献以及我们对phasiRNA位点独特的GC含量模式的额外观察,我们仅提出这一观点。组蛋白基因富含22个核苷酸长度的sRNA这一发现也表明存在染色质重塑。综上所述,我们获得了一些线索,使我们推测在单子叶植物玉米的雄性减数分裂过程中存在sRNA驱动的DNA甲基化以及可能的染色质重塑,这与先前的知识一致并加以扩展。