College of Horticulture, Nanjing Agricultural University, Nanjing 210095, China.
Physiol Plant. 2011 Jan;141(1):56-70. doi: 10.1111/j.1399-3054.2010.01411.x. Epub 2010 Oct 21.
Thirty-one potential miRNAs that belong to 16 miRNA families were discovered from more than 324 000 EST sequences of apple (Malus domestica). In addition, precise sequences, especially terminal nucleotides of the 16 apple miRNAs (mdo-miRNAs) in 16 families were validated by miR-RACE, a newly developed method for the determination of the potential miRNAs predicted computationally. The expression of these 16 microRNAs could be detected in apple young leaf, old leaf, young stem, flower bud, flower and developing fruits by quantitative RT-PCR (qRT-PCR) and some of them showed tissue-specific expression. Fifty-six potential targets were identified for the 16 apple miRNAs, most of which were transcription factors that play important roles in apple development. Twelve target genes were experimentally verified by qRT-PCR, with some exhibiting different expression trends from their corresponding microRNAs, indicating the cleavage mode of miRNAs on their target genes.
从超过 324000 个苹果(Malus domestica)的 EST 序列中发现了 31 个属于 16 个 miRNA 家族的潜在 miRNA。此外,通过新开发的用于确定计算预测的潜在 miRNA 的方法 miR-RACE,验证了 16 个家族中的 16 个苹果 miRNA(mdo-miRNAs)的精确序列,特别是末端核苷酸。通过定量 RT-PCR(qRT-PCR)可以在苹果幼叶、老叶、幼茎、芽、花和发育中的果实中检测到这些 16 种 microRNAs 的表达,其中一些表现出组织特异性表达。为 16 个苹果 miRNA 鉴定了 56 个潜在靶标,其中大多数是转录因子,它们在苹果发育中起重要作用。通过 qRT-PCR 实验验证了 12 个靶基因,其中一些靶基因的表达趋势与其相应的 microRNAs 不同,表明 miRNA 对其靶基因的切割模式。