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生物信息学分析表明拟南芥中转运RNA和微小RNA存在碱基修饰。

Bioinformatics analysis suggests base modifications of tRNAs and miRNAs in Arabidopsis thaliana.

作者信息

Iida Kei, Jin Hailing, Zhu Jian-Kang

机构信息

Department of Botany and Plant Sciences, University of California, Riverside, CA 92521, USA.

出版信息

BMC Genomics. 2009 Apr 9;10:155. doi: 10.1186/1471-2164-10-155.

DOI:10.1186/1471-2164-10-155
PMID:19358740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2674459/
Abstract

BACKGROUND

Modifications of RNA bases have been found in some mRNAs and non-coding RNAs including rRNAs, tRNAs, and snRNAs, where modified bases are important for RNA function. Little is known about RNA base modifications in Arabidopsis thaliana.

RESULTS

In the current work, we carried out a bioinformatics analysis of RNA base modifications in tRNAs and miRNAs using large numbers of cDNA sequences of small RNAs (sRNAs) generated with the 454 technology and the massively parallel signature sequencing (MPSS) method. We looked for sRNAs that map to the genome sequence with one-base mismatch (OMM), which indicate candidate modified nucleotides. We obtained 1,187 sites with possible RNA base modifications supported by both 454 and MPSS sequences. Seven hundred and three of these sites were within tRNA loci. Nucleotide substitutions were frequently located in the T arm (substitutions from A to U or G), upstream of the D arm (from G to C, U, or A), and downstream of the D arm (from G to U). The positions of major substitution sites corresponded with the following known RNA base modifications in tRNAs: N1-methyladenosine (m1A), N2-methylguanosine (m2G), and N2-N2-methylguanosine (m22G).

CONCLUSION

These results indicate that our bioinformatics method successfully detected modified nucleotides in tRNAs. Using this method, we also found 147 substitution sites in miRNA loci. As with tRNAs, substitutions from A to U or G and from G to C, U, or A were common, suggesting that base modifications might be similar in tRNAs and miRNAs. We suggest that miRNAs contain modified bases and such modifications might be important for miRNA maturation and/or function.

摘要

背景

在一些信使核糖核酸(mRNA)和非编码核糖核酸(RNA)中发现了核糖核酸碱基修饰,包括核糖体核糖核酸(rRNA)、转运核糖核酸(tRNA)和小核核糖核酸(snRNA),其中修饰碱基对RNA功能很重要。关于拟南芥中的核糖核酸碱基修饰知之甚少。

结果

在当前研究中,我们利用454技术和大规模平行签名测序(MPSS)方法生成的大量小RNA(sRNA)的互补脱氧核糖核酸(cDNA)序列,对tRNA和微小核糖核酸(miRNA)中的核糖核酸碱基修饰进行了生物信息学分析。我们寻找与基因组序列单碱基错配(OMM)的sRNA,这表明存在候选修饰核苷酸。我们获得了1187个可能的核糖核酸碱基修饰位点,454和MPSS序列均支持这些位点。其中703个位点位于tRNA基因座内。核苷酸替换经常位于T臂(从腺嘌呤(A)替换为尿嘧啶(U)或鸟嘌呤(G))、D臂上游(从G替换为胞嘧啶(C)、U或A)以及D臂下游(从G替换为U)。主要替换位点的位置与tRNA中以下已知的核糖核酸碱基修饰相对应:N1-甲基腺嘌呤(m1A)、N2-甲基鸟嘌呤(m2G)和N2-N2-甲基鸟嘌呤(m22G)。

结论

这些结果表明我们的生物信息学方法成功检测到了tRNA中的修饰核苷酸。使用该方法,我们还在miRNA基因座中发现了147个替换位点。与tRNA一样,从A替换为U或G以及从G替换为C、U或A很常见,这表明tRNA和miRNA中的碱基修饰可能相似。我们认为miRNA含有修饰碱基,这种修饰可能对miRNA的成熟和/或功能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/7111561c2a17/1471-2164-10-155-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/7fb7369a4c59/1471-2164-10-155-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/074d40a72816/1471-2164-10-155-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/c308e10e8eb0/1471-2164-10-155-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/22e935c26678/1471-2164-10-155-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/49d8a7211a73/1471-2164-10-155-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/7111561c2a17/1471-2164-10-155-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/7fb7369a4c59/1471-2164-10-155-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/074d40a72816/1471-2164-10-155-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/c308e10e8eb0/1471-2164-10-155-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/22e935c26678/1471-2164-10-155-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/49d8a7211a73/1471-2164-10-155-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2712/2674459/7111561c2a17/1471-2164-10-155-6.jpg

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