Ben Amor Besma, Wirth Sonia, Merchan Francisco, Laporte Philippe, d'Aubenton-Carafa Yves, Hirsch Judith, Maizel Alexis, Mallory Allison, Lucas Antoine, Deragon Jean Marc, Vaucheret Herve, Thermes Claude, Crespi Martin
Institut des Sciences du Végétal (ISV), CNRS, 91198 Gif-sur-Yvette, France.
Genome Res. 2009 Jan;19(1):57-69. doi: 10.1101/gr.080275.108. Epub 2008 Nov 7.
Long non-protein coding RNAs (npcRNA) represent an emerging class of riboregulators, which either act directly in this long form or are processed to shorter miRNA and siRNA. Genome-wide bioinformatic analysis of full-length cDNA databases identified 76 Arabidopsis npcRNAs. Fourteen npcRNAs were antisense to protein-coding mRNAs, suggesting cis-regulatory roles. Numerous 24-nt siRNA matched to five different npcRNAs, suggesting that these npcRNAs are precursors of this type of siRNA. Expression analyses of the 76 npcRNAs identified a novel npcRNA that accumulates in a dcl1 mutant but does not appear to produce trans-acting siRNA or miRNA. Additionally, another npcRNA was the precursor of miR869 and shown to be up-regulated in dcl4 but not in dcl1 mutants, indicative of a young miRNA gene. Abiotic stress altered the accumulation of 22 npcRNAs among the 76, a fraction significantly higher than that observed for the RNA binding protein-coding fraction of the transcriptome. Overexpression analyses in Arabidopsis identified two npcRNAs as regulators of root growth during salt stress and leaf morphology, respectively. Hence, together with small RNAs, long npcRNAs encompass a sensitive component of the transcriptome that have diverse roles during growth and differentiation.
长链非蛋白质编码RNA(npcRNA)代表了一类新兴的核糖调节因子,它们要么以这种长链形式直接发挥作用,要么被加工成较短的miRNA和siRNA。对全长cDNA数据库进行全基因组生物信息学分析,鉴定出76种拟南芥npcRNA。其中14种npcRNA与蛋白质编码mRNA呈反义关系,表明它们具有顺式调节作用。大量24个核苷酸的siRNA与5种不同的npcRNA匹配,表明这些npcRNA是这类siRNA的前体。对这76种npcRNA的表达分析鉴定出一种新型npcRNA,它在dcl1突变体中积累,但似乎不产生反式作用siRNA或miRNA。此外,另一种npcRNA是miR869的前体,在dcl4突变体中上调,但在dcl1突变体中未上调,这表明它是一个年轻的miRNA基因。非生物胁迫改变了76种npcRNA中的22种的积累,这一比例显著高于转录组中RNA结合蛋白编码部分的观察值。在拟南芥中的过表达分析分别鉴定出两种npcRNA作为盐胁迫期间根系生长和叶片形态的调节因子。因此,与小RNA一起,长链npcRNA构成了转录组的一个敏感成分,在生长和分化过程中具有多种作用。