An updated human snoRNAome

被引:191
作者
Jorjani, Hadi [1 ,2 ]
Kehr, Stephanie [3 ,4 ]
Jedlinski, Dominik J. [1 ,2 ]
Gumienny, Rafal [1 ,2 ]
Hertel, Jana [3 ,4 ]
Stadler, Peter F. [3 ,4 ,5 ,6 ,7 ,8 ]
Zavolan, Mihaela [1 ,2 ]
Gruber, Andreas R. [1 ,2 ]
机构
[1] Univ Basel, Biozentrum, Computat & Syst Biol, CH-4056 Basel, Switzerland
[2] Swiss Inst Bioinformat, CH-4056 Basel, Switzerland
[3] Univ Leipzig, Dept Comp Sci, Bioinformat Grp, D-04107 Leipzig, Germany
[4] Univ Leipzig, Interdisciplinary Ctr Bioinformat, D-04107 Leipzig, Germany
[5] Max Planck Inst Math Sci, D-04103 Leipzig, Germany
[6] Fraunhofer Inst Cell Therapy & Immunol, RNom Grp, D-04103 Leipzig, Germany
[7] Univ Vienna, Dept Theoret Chem, A-1090 Vienna, Austria
[8] Santa Fe Inst, Santa Fe, NM 87501 USA
基金
瑞士国家科学基金会;
关键词
SMALL NUCLEOLAR RNAS; BOX C/D SNORNAS; HUMAN TELOMERASE RNA; EFFICIENT TARGET PREDICTION; BODY-SPECIFIC LOCALIZATION; LONG NONCODING RNAS; 18S RIBOSOMAL-RNA; CAJAL BODY; PRERIBOSOMAL RNA; MESSENGER-RNA;
D O I
10.1093/nar/gkw386
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small nucleolar RNAs (snoRNAs) are a class of non-coding RNAs that guide the post-transcriptional processing of other non-coding RNAs (mostly ribosomal RNAs), but have also been implicated in processes ranging from microRNA-dependent gene silencing to alternative splicing. In order to construct an up-to-date catalog of human snoRNAs we have combined data from various databases, de novo prediction and extensive literature review. In total, we list more than 750 curated genomic loci that give rise to snoRNA and snoRNA-like genes. Utilizing small RNA-seq data from the ENCODE project, our study characterizes the plasticity of snoRNA expression identifying both constitutively as well as cell type specific expressed snoRNAs. Especially, the comparison of malignant to non-malignant tissues and cell types shows a dramatic perturbation of the snoRNA expression profile. Finally, we developed a high-throughput variant of the reverse-transcriptase-based method for identifying 2'-O-methyl modifications in RNAs termed RimSeq. Using the data from this and other high-throughput protocols together with previously reported modification sites and state-of-the-art target prediction methods we re-estimate the snoRNA target RNA interaction network. Our current results assign a reliable modification site to 83% of the canonical snoRNAs, leaving only 76 snoRNA sequences as orphan.
引用
收藏
页码:5068 / 5082
页数:15
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