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本文引用的文献

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Systematic analysis of posttranscriptional gene expression.系统分析转录后基因表达。
Wiley Interdiscip Rev Syst Biol Med. 2010 Mar-Apr;2(2):162-180. doi: 10.1002/wsbm.54.
2
miR-21 mediates fibrogenic activation of pulmonary fibroblasts and lung fibrosis.miR-21 介导肺成纤维细胞的纤维生成激活和肺纤维化。
J Exp Med. 2010 Aug 2;207(8):1589-97. doi: 10.1084/jem.20100035. Epub 2010 Jul 19.
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Proinflammatory role for let-7 microRNAS in experimental asthma.let-7 微 RNA 在实验性哮喘中的促炎作用。
J Biol Chem. 2010 Sep 24;285(39):30139-49. doi: 10.1074/jbc.M110.145698. Epub 2010 Jul 14.
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MicroRNA networks in mouse lung organogenesis.小鼠肺器官发生中的 microRNA 网络。
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Post-transcriptional control during chronic inflammation and cancer: a focus on AU-rich elements.慢性炎症和癌症中的转录后调控:以富含 AU 的元件为重点。
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Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP.通过 PAR-CLIP 技术在转录组范围内鉴定 RNA 结合蛋白和 microRNA 的靶位。
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Multiple levels of post-transcriptional control of expression of the poly (A)-binding protein.多水平的转录后调控多聚(A)结合蛋白的表达。
RNA Biol. 2010 Jan-Feb;7(1):5-12. doi: 10.4161/rna.7.1.10256. Epub 2010 Jan 6.
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High-resolution analysis of DNA regulatory elements by synthetic saturation mutagenesis.通过合成饱和诱变对 DNA 调控元件进行高分辨率分析。
Nat Biotechnol. 2009 Dec;27(12):1173-5. doi: 10.1038/nbt.1589.
9
UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs.UTRdb 和 UTRsite(RELEASE 2010):真核 mRNA 非翻译区序列和调控模体的集合。
Nucleic Acids Res. 2010 Jan;38(Database issue):D75-80. doi: 10.1093/nar/gkp902. Epub 2009 Oct 30.
10
Antagonism of microRNA-126 suppresses the effector function of TH2 cells and the development of allergic airways disease.微小RNA-126的拮抗作用可抑制TH2细胞的效应功能及变应性气道疾病的发展。
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为了系统地理解 mRNA 3' 非翻译区。

Toward a systematic understanding of mRNA 3' untranslated regions.

机构信息

Department of Medicine, University of California, San Francisco, CA, USA.

出版信息

Proc Am Thorac Soc. 2011 May;8(2):163-6. doi: 10.1513/pats.201007-054MS.

DOI:10.1513/pats.201007-054MS
PMID:21543795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3131834/
Abstract

Messenger RNAs (mRNAs) contain prominent untranslated regions (UTRs) that are increasingly recognized to play roles in mRNA processing, transport, stability, and translation. 3' UTRs are believed to harbor recognition sites for a diverse set of RNA-binding proteins that regulate gene expression as well as most active microRNA target sites. Although the roles of 3' UTRs in the normal and diseased lung have not yet been studied extensively, available evidence suggests important roles for 3' UTRs in lung development, inflammation, asthma, pulmonary fibrosis, and cancer. Systematic, genome-wide approaches are beginning to catalog functional elements within 3' UTRs and identify the proteins and microRNAs that interact with these elements. Application of new data sets and experimental approaches should provide powerful insights into how 3' UTR-mediated regulatory events contribute to disease and may inspire novel therapeutic approaches.

摘要

信使 RNA(mRNA)含有突出的非翻译区(UTR),这些区域越来越被认为在 mRNA 处理、运输、稳定性和翻译中发挥作用。3'UTR 被认为含有一组不同的 RNA 结合蛋白的识别位点,这些蛋白调节基因表达以及大多数活跃的 microRNA 靶位点。尽管 3'UTR 在正常和患病肺部中的作用尚未得到广泛研究,但现有证据表明 3'UTR 在肺发育、炎症、哮喘、肺纤维化和癌症中发挥着重要作用。系统的、全基因组的方法开始对 3'UTR 内的功能元件进行编目,并确定与这些元件相互作用的蛋白质和 microRNA。新数据集和实验方法的应用应该为 3'UTR 介导的调节事件如何导致疾病提供有力的见解,并可能激发新的治疗方法。