Reid Jeffrey G, Nagaraja Ankur K, Lynn Francis C, Drabek Rafal B, Muzny Donna M, Shaw Chad A, Weiss Michelle K, Naghavi Arash O, Khan Mahjabeen, Zhu Huifeng, Tennakoon Jayantha, Gunaratne Gemunu H, Corry David B, Miller Jonathan, McManus Michael T, German Michael S, Gibbs Richard A, Matzuk Martin M, Gunaratne Preethi H
Department of Chemistry, University of Houston, Houston, Texas 77204, USA.
Genome Res. 2008 Oct;18(10):1571-81. doi: 10.1101/gr.078246.108. Epub 2008 Jul 9.
Massively parallel sequencing of millions of < 30-nt RNAs expressed in mouse ovary, embryonic pancreas (E14.5), and insulin-secreting beta-cells (betaTC-3) reveals that approximately 50% of the mature miRNAs representing mostly the mmu-let-7 family display internal insertion/deletions and substitutions when compared to precursor miRNA and the mouse genome reference sequences. Approximately, 12%-20% of species associated with mmu-let-7 populations exhibit sequence discrepancies that are dramatically reduced in nucleotides 3-7 (5'-seed) and 10-15 (cleavage and anchor sites). This observation is inconsistent with sequencing error and leads us to propose that the changes arise predominantly from post-transcriptional RNA-editing activity operating on miRNA:target mRNA complexes. Internal nucleotide modifications are most enriched at the ninth nucleotide position. A common ninth base edit of U-to-G results in a significant increase in stability of down-regulated let-7a targets in inhibin-deficient mice (Inha-/-). An excess of U-insertions (14.8%) over U-deletions (1.5%) and the presence of cleaved intermediates suggest that a mammalian TUTase (terminal uridylyl transferase) mediated dUTP-dependent U-insertion/U-deletion cycle may be a possible mechanism. We speculate that mRNA target site-directed editing of mmu-let-7a duplex-bulges stabilizes "loose" miRNA:mRNA target associations and functions to expand the target repertoire and/or enhance mRNA decay over translational repression. Our results also demonstrate that the systematic study of sequence variation within specific RNA classes in a given cell type from millions of sequences generated by next-generation sequencing (NGS) technologies ("intranomics") can be used broadly to infer functional constraints on specific parts of completely uncharacterized RNAs.
对数以百万计在小鼠卵巢、胚胎胰腺(E14.5)和胰岛素分泌β细胞(βTC-3)中表达的小于30个核苷酸的RNA进行大规模平行测序,结果显示,与前体miRNA和小鼠基因组参考序列相比,约50%的成熟miRNA(主要代表mmu-let-7家族)存在内部插入/缺失和替换。与mmu-let-7群体相关的约12%-20%的序列在核苷酸3-7(5'-种子区)和10-15(切割和锚定位点)处的序列差异显著减少。这一观察结果与测序错误不一致,促使我们提出这些变化主要源于对miRNA:靶mRNA复合物进行的转录后RNA编辑活动。内部核苷酸修饰在第九个核苷酸位置最为丰富。U到G的常见第九位碱基编辑导致抑制素缺陷小鼠(Inha-/-)中let-7a下调靶标的稳定性显著增加。U插入(14.8%)超过U缺失(1.5%)的过量以及切割中间体的存在表明,哺乳动物末端尿苷酰转移酶(TUTase)介导的依赖dUTP的U插入/U缺失循环可能是一种可能的机制。我们推测,mmu-let-7a双链体凸起的mRNA靶位点定向编辑稳定了“松散”的miRNA:mRNA靶标关联,并起到扩展靶标库和/或增强mRNA降解而非翻译抑制的作用。我们的结果还表明,通过下一代测序(NGS)技术从给定细胞类型中的数百万个序列对特定RNA类别内的序列变异进行系统研究(“内部组学”)可广泛用于推断对完全未表征RNA特定部分的功能限制。