• 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

胚胎干细胞 miRNA 及其在发育和疾病中的作用。

Embryonic stem cell miRNAs and their roles in development and disease.

机构信息

Memorial Sloan-Kettering Cancer Center, Cancer Biology and Genetics Program, New York, NY 10065, United States.

出版信息

Semin Cancer Biol. 2012 Oct;22(5-6):428-36. doi: 10.1016/j.semcancer.2012.04.009. Epub 2012 May 4.

DOI:10.1016/j.semcancer.2012.04.009
PMID:22561239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3426648/
Abstract

MicroRNAs have emerged as important modulators of gene expression. Both during development and disease, regulation by miRNAs controls the choice between self-renewal and differentiation, survival and apoptosis and dictates how cells respond to external stimuli. In mouse pluripotent embryonic stem cells, a surprisingly small set of miRNAs, encoded by four polycistronic genes is at the center of such decisions. miR-290-295, miR-302-367, miR-17-92 and miR-106b-25 encode for miRNAs with highly related sequences that seem to control largely overlapping gene sets. Recent studies have highlighted the importance of these miRNAs in the maintenance of 'stemness' and regulation of normal development and have linked the deregulation of their expression to a variety of human diseases.

摘要

微小 RNA 已成为基因表达的重要调控因子。无论是在发育过程中还是在疾病中,miRNA 的调控都控制着自我更新和分化、生存和凋亡之间的选择,并决定了细胞如何对外界刺激做出反应。在小鼠多能胚胎干细胞中,一小部分 miRNA 由四个多顺反子基因编码,处于这些决定的中心。miR-290-295、miR-302-367、miR-17-92 和 miR-106b-25 编码具有高度相关序列的 miRNA,似乎控制着大部分重叠的基因集。最近的研究强调了这些 miRNA 在维持“干性”和调节正常发育中的重要性,并将它们表达的失调与多种人类疾病联系起来。

相似文献

1
Embryonic stem cell miRNAs and their roles in development and disease.胚胎干细胞 miRNA 及其在发育和疾病中的作用。
Semin Cancer Biol. 2012 Oct;22(5-6):428-36. doi: 10.1016/j.semcancer.2012.04.009. Epub 2012 May 4.
2
Embryonic stem cell microRNAs: defining factors in induced pluripotent (iPS) and cancer (CSC) stem cells?胚胎干细胞微小RNA:诱导多能干细胞(iPS)和癌症干细胞(CSC)的决定性因素?
Curr Stem Cell Res Ther. 2009 Sep;4(3):168-77. doi: 10.2174/157488809789057400.
3
MicroRNAs in embryonic stem cells and early embryonic development.胚胎干细胞和早期胚胎发育中的微小RNA
J Cell Mol Med. 2008 Dec;12(6A):2181-8. doi: 10.1111/j.1582-4934.2008.00513.x.
4
The Expression and Functional Roles of miRNAs in Embryonic and Lineage-Specific Stem Cells.miRNAs 在胚胎和谱系特异性干细胞中的表达和功能作用。
Curr Stem Cell Res Ther. 2019;14(3):278-289. doi: 10.2174/1574888X14666190123162402.
5
MicroRNA and gene expression patterns in the differentiation of human embryonic stem cells.人类胚胎干细胞分化过程中的微小RNA与基因表达模式
J Transl Med. 2009 Mar 23;7:20. doi: 10.1186/1479-5876-7-20.
6
Bioinformatics and microarray analysis of microRNA expression profiles of murine embryonic stem cells, neural stem cells induced from ESCs and isolated from E8.5 mouse neural tube.小鼠胚胎干细胞、由胚胎干细胞诱导而来的神经干细胞以及从E8.5小鼠神经管分离出的神经干细胞的微小RNA表达谱的生物信息学与微阵列分析
Neurol Res. 2010 Jul;32(6):603-13. doi: 10.1179/174313209X455691. Epub 2009 Aug 5.
7
Vitamin C induces a pluripotent state in mouse embryonic stem cells by modulating microRNA expression.维生素 C 通过调节 microRNA 表达诱导小鼠胚胎干细胞多能性。
FEBS J. 2015 Feb;282(4):685-99. doi: 10.1111/febs.13173. Epub 2015 Jan 8.
8
Evolutionary emergence of microRNAs in human embryonic stem cells.人类胚胎干细胞中微小RNA的进化起源
PLoS One. 2008 Jul 30;3(7):e2820. doi: 10.1371/journal.pone.0002820.
9
microRNAs: important regulators of stem cells.微小RNA:干细胞的重要调节因子。
Stem Cell Res Ther. 2017 May 11;8(1):110. doi: 10.1186/s13287-017-0551-0.
10
The Key Role of MicroRNAs in Self-Renewal and Differentiation of Embryonic Stem Cells.微小 RNA 在胚胎干细胞自我更新和分化中的关键作用。
Int J Mol Sci. 2020 Aug 31;21(17):6285. doi: 10.3390/ijms21176285.

引用本文的文献

1
The miR-290 and miR-302 clusters are essential for reprogramming of fibroblasts to induced pluripotent stem cells.miR-290和miR-302基因簇对于将成纤维细胞重编程为诱导多能干细胞至关重要。
Stem Cells. 2025 Feb 12;43(2). doi: 10.1093/stmcls/sxae080.
2
The miR-290 and miR-302 clusters are essential for reprogramming of fibroblasts to induced pluripotent stem cells.miR-290和miR-302基因簇对于将成纤维细胞重编程为诱导多能干细胞至关重要。
bioRxiv. 2024 Sep 3:2024.09.02.610895. doi: 10.1101/2024.09.02.610895.
3
Human Embryonic Stem-Cell-Derived Exosomes Repress NLRP3 Inflammasome to Alleviate Pyroptosis in Nucleus Pulposus Cells by Transmitting miR-302c.人胚胎干细胞衍生的外泌体通过传递 miR-302c 抑制 NLRP3 炎症小体从而减轻髓核细胞的细胞焦亡。
Int J Mol Sci. 2023 Apr 21;24(8):7664. doi: 10.3390/ijms24087664.
4
A Comprehensive Sequencing Analysis of Testis-Born miRNAs in Immature and Mature Indigenous Wandong Cattle ().不成熟和成熟的本土万州牛睾丸来源 miRNAs 的全面测序分析( )。
Genes (Basel). 2022 Nov 23;13(12):2185. doi: 10.3390/genes13122185.
5
acts as a tumor suppressor by negatively regulating the cluster.通过负向调节该簇发挥肿瘤抑制作用。
Mol Ther Nucleic Acids. 2021 Oct 21;26:1148-1158. doi: 10.1016/j.omtn.2021.10.021. eCollection 2021 Dec 3.
6
Live-cell imaging of microRNA expression with post-transcriptional feedback control.具有转录后反馈控制的微小RNA表达的活细胞成像
Mol Ther Nucleic Acids. 2021 Aug 26;26:547-556. doi: 10.1016/j.omtn.2021.08.018. eCollection 2021 Dec 3.
7
Restoration of RNA helicase DDX5 suppresses hepatitis B virus (HBV) biosynthesis and Wnt signaling in HBV-related hepatocellular carcinoma.RNA 解旋酶 DDX5 的恢复抑制乙型肝炎病毒 (HBV) 相关肝细胞癌中的 HBV 生物合成和 Wnt 信号通路。
Theranostics. 2020 Sep 1;10(24):10957-10972. doi: 10.7150/thno.49629. eCollection 2020.
8
Epigenetic Inheritance: Concepts, Mechanisms and Perspectives.表观遗传继承:概念、机制与展望。
Front Mol Neurosci. 2018 Sep 28;11:292. doi: 10.3389/fnmol.2018.00292. eCollection 2018.
9
miR-7 Modulates hESC Differentiation into Insulin-Producing Beta-like Cells and Contributes to Cell Maturation.微小RNA-7调控人胚胎干细胞分化为胰岛素分泌β样细胞并促进细胞成熟。
Mol Ther Nucleic Acids. 2018 Sep 7;12:463-477. doi: 10.1016/j.omtn.2018.06.002. Epub 2018 Jun 15.
10
Roles of microRNAs in mammalian reproduction: from the commitment of germ cells to peri-implantation embryos.微小 RNA 在哺乳动物生殖中的作用:从生殖细胞的决定到着床前胚胎。
Biol Rev Camb Philos Soc. 2019 Apr;94(2):415-438. doi: 10.1111/brv.12459. Epub 2018 Aug 27.

本文引用的文献

1
Capture of microRNA-bound mRNAs identifies the tumor suppressor miR-34a as a regulator of growth factor signaling.微 RNA 结合 mRNA 的捕获鉴定肿瘤抑制因子 miR-34a 作为生长因子信号的调节剂。
PLoS Genet. 2011 Nov;7(11):e1002363. doi: 10.1371/journal.pgen.1002363. Epub 2011 Nov 10.
2
Molecular basis for interaction of let-7 microRNAs with Lin28.Let-7 微 RNA 与 Lin28 相互作用的分子基础。
Cell. 2011 Nov 23;147(5):1080-91. doi: 10.1016/j.cell.2011.10.020. Epub 2011 Nov 10.
3
miR-34 miRNAs provide a barrier for somatic cell reprogramming.miR-34 miRNAs 为体细胞重编程提供了一道屏障。
Nat Cell Biol. 2011 Oct 23;13(11):1353-60. doi: 10.1038/ncb2366.
4
Genome-wide identification of microRNA targets in human ES cells reveals a role for miR-302 in modulating BMP response.人类胚胎干细胞中 miRNA 靶基因的全基因组鉴定揭示了 miR-302 在调节 BMP 反应中的作用。
Genes Dev. 2011 Oct 15;25(20):2173-86. doi: 10.1101/gad.17221311.
5
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.胚系缺失 miR-17∼92 簇导致人类骨骼和生长缺陷。
Nat Genet. 2011 Sep 4;43(10):1026-30. doi: 10.1038/ng.915.
6
MicroRNAs can generate thresholds in target gene expression.微小 RNA 可以在靶基因表达中产生阈值。
Nat Genet. 2011 Aug 21;43(9):854-9. doi: 10.1038/ng.905.
7
Mir-290-295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects.miR-290-295 缺失的小鼠表现为部分显性胚胎致死和生殖细胞缺陷。
Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):14163-8. doi: 10.1073/pnas.1111241108. Epub 2011 Aug 15.
8
miR-17~92 cooperates with RB pathway mutations to promote retinoblastoma.miR-17~92 与 RB 通路突变协同促进视网膜母细胞瘤。
Genes Dev. 2011 Aug 15;25(16):1734-45. doi: 10.1101/gad.17027411. Epub 2011 Aug 4.
9
The miR 302-367 cluster drastically affects self-renewal and infiltration properties of glioma-initiating cells through CXCR4 repression and consequent disruption of the SHH-GLI-NANOG network.miR 302-367 簇通过抑制 CXCR4 及其随后破坏 SHH-GLI-NANOG 网络,极大地影响了神经胶质瘤起始细胞的自我更新和浸润特性。
Cell Death Differ. 2012 Feb;19(2):232-44. doi: 10.1038/cdd.2011.89. Epub 2011 Jul 1.
10
Multiple targets of miR-302 and miR-372 promote reprogramming of human fibroblasts to induced pluripotent stem cells.miR-302 和 miR-372 的多个靶标促进人成纤维细胞重编程为诱导多能干细胞。
Nat Biotechnol. 2011 May;29(5):443-8. doi: 10.1038/nbt.1862. Epub 2011 Apr 13.