• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Determinants of targeting by endogenous and exogenous microRNAs and siRNAs.内源性和外源性微小RNA及小干扰RNA靶向作用的决定因素。
RNA. 2007 Nov;13(11):1894-910. doi: 10.1261/rna.768207. Epub 2007 Sep 13.
2
siRNAs can function as miRNAs.小干扰RNA可以发挥微小RNA的功能。
Genes Dev. 2003 Feb 15;17(4):438-42. doi: 10.1101/gad.1064703.
3
HIV-1 TAR element is processed by Dicer to yield a viral micro-RNA involved in chromatin remodeling of the viral LTR.HIV-1 TAR元件由Dicer加工,产生一种参与病毒LTR染色质重塑的病毒微小RNA。
BMC Mol Biol. 2007 Jul 30;8:63. doi: 10.1186/1471-2199-8-63.
4
MicroRNA targeting specificity in mammals: determinants beyond seed pairing.哺乳动物中微小RNA的靶向特异性:种子配对之外的决定因素。
Mol Cell. 2007 Jul 6;27(1):91-105. doi: 10.1016/j.molcel.2007.06.017.
5
DEAD-box RNA helicase subunits of the Drosha complex are required for processing of rRNA and a subset of microRNAs.Drosha复合物的DEAD盒RNA解旋酶亚基是rRNA和一部分微小RNA加工所必需的。
Nat Cell Biol. 2007 May;9(5):604-11. doi: 10.1038/ncb1577. Epub 2007 Apr 15.
6
Transfection of siRNAs can alter miRNA levels and trigger non-specific protein degradation in mammalian cells.在哺乳动物细胞中,小干扰RNA(siRNA)的转染可改变微小RNA(miRNA)水平并引发非特异性蛋白质降解。
Biochim Biophys Acta. 2013 May;1829(5):455-68. doi: 10.1016/j.bbagrm.2013.01.011. Epub 2013 Feb 8.
7
MicroRNA Seed Region Length Impact on Target Messenger RNA Expression and Survival in Colorectal Cancer.微小RNA种子区域长度对结直肠癌中靶信使核糖核酸表达及生存的影响
PLoS One. 2016 Apr 28;11(4):e0154177. doi: 10.1371/journal.pone.0154177. eCollection 2016.
8
Distance constraints between microRNA target sites dictate efficacy and cooperativity.微小RNA靶位点之间的距离限制决定了其有效性和协同性。
Nucleic Acids Res. 2007;35(7):2333-42. doi: 10.1093/nar/gkm133. Epub 2007 Mar 27.
9
Mouse ES cells express endogenous shRNAs, siRNAs, and other Microprocessor-independent, Dicer-dependent small RNAs.小鼠胚胎干细胞表达内源性短发夹RNA、小干扰RNA以及其他不依赖微处理器、依赖Dicer的小RNA。
Genes Dev. 2008 Oct 15;22(20):2773-85. doi: 10.1101/gad.1705308.
10
Stimuli-dependent cleavage of Dicer during apoptosis.凋亡过程中Dicer的刺激依赖性切割。
Biochem J. 2008 Jun 15;412(3):527-34. doi: 10.1042/BJ20071461.

引用本文的文献

1
MicroRNAs and Their Inhibition in Modulating Expression in the Context of Papillary Thyroid Carcinoma.微小RNA及其在甲状腺乳头状癌背景下对基因表达调控中的抑制作用
Int J Mol Sci. 2025 Aug 15;26(16):7889. doi: 10.3390/ijms26167889.
2
Clinical significance of long non-coding RNA MIR155HG genetic variants and susceptibility to oral cancer.长链非编码RNA MIR155HG基因变异与口腔癌易感性的临床意义
Sci Rep. 2025 Mar 22;15(1):9956. doi: 10.1038/s41598-025-94661-3.
3
In-Depth Analysis of miRNA Binding Sites Reveals the Complex Response of Uterine Epithelium to miR-26a-5p and miR-125b-5p During Early Pregnancy.对miRNA结合位点的深入分析揭示了妊娠早期子宫上皮对miR-26a-5p和miR-125b-5p的复杂反应。
Mol Cell Proteomics. 2025 Jan;24(1):100879. doi: 10.1016/j.mcpro.2024.100879. Epub 2024 Nov 12.
4
Stage-specific expression patterns and co-targeting relationships among miRNAs in the developing mouse cerebral cortex.发育中的小鼠大脑皮层中 miRNA 的阶段特异性表达模式和共同靶向关系。
Commun Biol. 2024 Oct 22;7(1):1366. doi: 10.1038/s42003-024-07092-7.
5
Unraveling the Regulatory Role of HuR/microRNA Axis in Colorectal Cancer Tumorigenesis.解析HuR/微小RNA轴在结直肠癌发生中的调控作用
Cancers (Basel). 2024 Sep 18;16(18):3183. doi: 10.3390/cancers16183183.
6
A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match.高分辨率的功能性 miR-181 反应元件图谱在胸腺中揭示了编码序列靶向和替代种子匹配的作用。
Nucleic Acids Res. 2024 Aug 12;52(14):8515-8533. doi: 10.1093/nar/gkae416.
7
Advanced computational predictive models of miRNA-mRNA interaction efficiency.miRNA与mRNA相互作用效率的高级计算预测模型。
Comput Struct Biotechnol J. 2024 Apr 19;23:1740-1754. doi: 10.1016/j.csbj.2024.04.015. eCollection 2024 Dec.
8
Experimental capture of miRNA targetomes: disease-specific 3'UTR library-based miRNA targetomics for Parkinson's disease.实验捕获 miRNA 靶标组:基于疾病特异性 3'UTR 文库的帕金森病 miRNA 靶标组学。
Exp Mol Med. 2024 Apr;56(4):935-945. doi: 10.1038/s12276-024-01202-5. Epub 2024 Apr 1.
9
New plasma diagnostic markers for colorectal cancer: transporter fragments of glutamate tRNA origin.结直肠癌新的血浆诊断标志物:谷氨酸tRNA来源的转运体片段
J Cancer. 2024 Jan 12;15(5):1299-1313. doi: 10.7150/jca.92102. eCollection 2024.
10
New prospects of environmental RNA metabarcoding research in biological diversity, ecotoxicological monitoring, and detection of COVID-19: a critical review.环境 RNA 代谢组学研究在生物多样性、生态毒理学监测和 COVID-19 检测方面的新前景:批判性评价。
Environ Sci Pollut Res Int. 2024 Feb;31(8):11406-11427. doi: 10.1007/s11356-023-31776-y. Epub 2024 Jan 6.

本文引用的文献

1
Spatial preferences of microRNA targets in 3' untranslated regions.3'非翻译区中微小RNA靶标的空间偏好性。
BMC Genomics. 2007 Jun 7;8:152. doi: 10.1186/1471-2164-8-152.
2
An mRNA m7G cap binding-like motif within human Ago2 represses translation.人类AGO2蛋白中一个类似mRNA m7G帽结合的基序可抑制翻译。
Cell. 2007 Jun 15;129(6):1141-51. doi: 10.1016/j.cell.2007.05.016. Epub 2007 May 24.
3
Requirement of bic/microRNA-155 for normal immune function.正常免疫功能对Bic/微小RNA - 155的需求。
Science. 2007 Apr 27;316(5824):608-11. doi: 10.1126/science.1139253.
4
Distance constraints between microRNA target sites dictate efficacy and cooperativity.微小RNA靶位点之间的距离限制决定了其有效性和协同性。
Nucleic Acids Res. 2007;35(7):2333-42. doi: 10.1093/nar/gkm133. Epub 2007 Mar 27.
5
AU-rich-element-mediated upregulation of translation by FXR1 and Argonaute 2.富含AU元件介导的FXR1和AGO2对翻译的上调作用
Cell. 2007 Mar 23;128(6):1105-18. doi: 10.1016/j.cell.2007.01.038.
6
Inference of miRNA targets using evolutionary conservation and pathway analysis.利用进化保守性和通路分析推断微小RNA靶标
BMC Bioinformatics. 2007 Mar 1;8:69. doi: 10.1186/1471-2105-8-69.
7
Effects of Dicer and Argonaute down-regulation on mRNA levels in human HEK293 cells.Dicer和Argonaute表达下调对人胚肾293细胞mRNA水平的影响。
Nucleic Acids Res. 2006;34(17):4801-15. doi: 10.1093/nar/gkl646. Epub 2006 Sep 13.
8
Designing siRNA that distinguish between genes that differ by a single nucleotide.设计能够区分仅相差一个核苷酸的基因的小干扰RNA。
PLoS Genet. 2006 Sep 8;2(9):e140. doi: 10.1371/journal.pgen.0020140. Epub 2006 Jul 24.
9
Relief of microRNA-mediated translational repression in human cells subjected to stress.在遭受应激的人类细胞中,微小RNA介导的翻译抑制得以缓解。
Cell. 2006 Jun 16;125(6):1111-24. doi: 10.1016/j.cell.2006.04.031.
10
Position-specific chemical modification of siRNAs reduces "off-target" transcript silencing.小干扰RNA的位点特异性化学修饰可减少“脱靶”转录本沉默。
RNA. 2006 Jul;12(7):1197-205. doi: 10.1261/rna.30706. Epub 2006 May 8.

内源性和外源性微小RNA及小干扰RNA靶向作用的决定因素。

Determinants of targeting by endogenous and exogenous microRNAs and siRNAs.

作者信息

Nielsen Cydney B, Shomron Noam, Sandberg Rickard, Hornstein Eran, Kitzman Jacob, Burge Christopher B

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

RNA. 2007 Nov;13(11):1894-910. doi: 10.1261/rna.768207. Epub 2007 Sep 13.

DOI:10.1261/rna.768207
PMID:17872505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2040081/
Abstract

Vertebrate mRNAs are frequently targeted for post-transcriptional repression by microRNAs (miRNAs) through mechanisms involving pairing of 3' UTR seed matches to bases at the 5' end of miRNAs. Through analysis of expression array data following miRNA or siRNA overexpression or inhibition, we found that mRNA fold change increases multiplicatively (i.e., log-additively) with seed match count and that a single 8 mer seed match mediates down-regulation comparable to two 7 mer seed matches. We identified several targeting determinants that enhance seed match-associated mRNA repression, including the presence of adenosine opposite miRNA base 1 and of adenosine or uridine opposite miRNA base 9, independent of complementarity to the siRNA/miRNA. Increased sequence conservation in the approximately 50 bases 5' and 3' of the seed match and increased AU content 3' of the seed match were each independently associated with increased mRNA down-regulation. All of these determinants are enriched in the vicinity of conserved miRNA seed matches, supporting their activity in endogenous miRNA targeting. Together, our results enable improved siRNA off-target prediction, allow integrated ranking of conserved and nonconserved miRNA targets, and show that targeting by endogenous and exogenous miRNAs/siRNAs involves similar or identical determinants.

摘要

脊椎动物的信使核糖核酸(mRNAs)经常受到微小核糖核酸(miRNAs)转录后抑制的作用,其机制涉及3'非翻译区(UTR)种子匹配与miRNAs 5'端碱基的配对。通过对miRNA或小干扰核糖核酸(siRNA)过表达或抑制后表达阵列数据的分析,我们发现mRNA的倍数变化随种子匹配数呈乘法增加(即对数相加),并且单个8聚体种子匹配介导的下调作用与两个7聚体种子匹配相当。我们确定了几个增强种子匹配相关mRNA抑制的靶向决定因素,包括与miRNA第1位碱基相对的腺苷以及与miRNA第9位碱基相对的腺苷或尿苷的存在,这与对siRNA/miRNA的互补性无关。种子匹配5'端和3'端约50个碱基处序列保守性的增加以及种子匹配3'端AU含量的增加均各自独立地与mRNA下调增加相关。所有这些决定因素在保守的miRNA种子匹配附近富集,支持它们在内源性miRNA靶向中的活性。总之,我们的结果改进了siRNA脱靶预测,实现了对保守和非保守miRNA靶标的综合排名,并表明内源性和外源性miRNAs/siRNAs的靶向涉及相似或相同的决定因素。