• 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
An evolutionarily conserved, alternatively spliced, intron in the p68/DDX5 DEAD-box RNA helicase gene encodes a novel miRNA.一个进化上保守的、可变剪接的 p68/DDX5 DEAD-box RNA 解旋酶基因内含子编码一个新的 miRNA。
RNA. 2011 Apr;17(4):555-62. doi: 10.1261/rna.2591611. Epub 2011 Feb 23.
2
The role of DEAD-box RNA helicase p68 (DDX5) in the development and treatment of breast cancer.DEAD-box RNA 解旋酶 p68(DDX5)在乳腺癌发生发展及治疗中的作用。
J Cell Physiol. 2019 May;234(5):5478-5487. doi: 10.1002/jcp.26912. Epub 2018 Nov 11.
3
P68 RNA Helicase (DDX5) Required for the Formation of Various Specific and Mature miRNA Active RISC Complexes.P68 RNA 解旋酶(DDX5)是形成各种特定和成熟的 miRNA 活性 RISCs 复合物所必需的。
Microrna. 2022;11(1):36-44. doi: 10.2174/2211536611666220218121640.
4
The DEAD-box RNA helicase DDX5 (p68) and β-catenin: The crucial regulators of FOXM1 gene expression in arbitrating colorectal cancer.DEAD-box RNA 解旋酶 DDX5(p68)和 β-连环蛋白:在调节结直肠癌细胞中 FOXM1 基因表达中的关键调控因子。
Biochim Biophys Acta Gene Regul Mech. 2023 Jun;1866(2):194933. doi: 10.1016/j.bbagrm.2023.194933. Epub 2023 Mar 29.
5
Structure and expression of the human p68 RNA helicase gene.人类p68 RNA解旋酶基因的结构与表达
Nucleic Acids Res. 2000 Feb 15;28(4):932-9. doi: 10.1093/nar/28.4.932.
6
Expression of the 'dead box' RNA helicase p68 is developmentally and growth regulated and correlates with organ differentiation/maturation in the fetus.“死亡盒”RNA解旋酶p68的表达受发育和生长调控,且与胎儿器官分化/成熟相关。
J Pathol. 1998 Apr;184(4):351-9. doi: 10.1002/(SICI)1096-9896(199804)184:4<351::AID-PATH1235>3.0.CO;2-C.
7
Regulation of MicroRNA 183 by Cyclooxygenase 2 in Liver Is DEAD-Box Helicase p68 (DDX5) Dependent: Role in Insulin Signaling.肝脏中环氧合酶2对微小RNA 183的调控依赖于DEAD盒解旋酶p68(DDX5):在胰岛素信号传导中的作用
Mol Cell Biol. 2015 Jul;35(14):2554-67. doi: 10.1128/MCB.00198-15. Epub 2015 May 11.
8
Downregulation of p68 RNA Helicase (DDX5) Activates a Survival Pathway Involving mTOR and MDM2 Signals.p68 RNA解旋酶(DDX5)的下调激活了一条涉及mTOR和MDM2信号的生存途径。
Folia Biol (Praha). 2017;63(2):52-59. doi: 10.14712/fb2017063020052.
9
The RNA helicase p68 is a novel androgen receptor coactivator involved in splicing and is overexpressed in prostate cancer.RNA解旋酶p68是一种参与剪接的新型雄激素受体共激活因子,在前列腺癌中过表达。
Cancer Res. 2008 Oct 1;68(19):7938-46. doi: 10.1158/0008-5472.CAN-08-0932.
10
A novel function for the DEAD-box RNA helicase DDX-23 in primary microRNA processing in Caenorhabditis elegans.DEAD盒RNA解旋酶DDX-23在秀丽隐杆线虫初级微小RNA加工中的新功能。
Dev Biol. 2016 Jan 15;409(2):459-72. doi: 10.1016/j.ydbio.2015.11.011. Epub 2015 Nov 18.

引用本文的文献

1
Transcriptome profiling in Rift Valley fever virus infected cells reveals modified transcriptional and alternative splicing programs.转录组谱分析显示裂谷热病毒感染细胞中修改的转录和可变剪接程序。
PLoS One. 2019 May 28;14(5):e0217497. doi: 10.1371/journal.pone.0217497. eCollection 2019.
2
P68 RNA helicase promotes invasion of glioma cells through negatively regulating DUSP5.P68 RNA 解旋酶通过负调控 DUSP5 促进胶质瘤细胞的侵袭。
Cancer Sci. 2019 Jan;110(1):107-117. doi: 10.1111/cas.13858. Epub 2018 Dec 3.
3
Detecting heterogeneity in single-cell RNA-Seq data by non-negative matrix factorization.通过非负矩阵分解检测单细胞RNA测序数据中的异质性。
PeerJ. 2017 Jan 19;5:e2888. doi: 10.7717/peerj.2888. eCollection 2017.
4
Regulation of mRNA Levels by Decay-Promoting Introns that Recruit the Exosome Specificity Factor Mmi1.通过招募外切体特异性因子Mmi1的促衰变内含子对mRNA水平进行调控。
Cell Rep. 2015 Dec 22;13(11):2504-2515. doi: 10.1016/j.celrep.2015.11.026. Epub 2015 Dec 6.
5
Identification and validation of a novel microRNA-like molecule derived from a cytoplasmic RNA virus antigenome by bioinformatics and experimental approaches.通过生物信息学和实验方法鉴定和验证源自细胞质 RNA 病毒抗原基因组的新型微小 RNA 样分子。
Virol J. 2014 Jul 1;11:121. doi: 10.1186/1743-422X-11-121.
6
A DEAD-box RNA helicase produces two forms of transcript that differentially respond to cold stress in a cryophyte (Chorispora bungeana).一种DEAD盒RNA解旋酶产生两种转录本形式,它们对低温植物( Bungeana地肤)中的冷胁迫有不同反应。
Planta. 2014 Aug;240(2):369-80. doi: 10.1007/s00425-014-2091-5. Epub 2014 May 27.
7
Novel SNPs and INDEL polymorphisms in the 3'UTR of DGAT1 gene: in silico analyses and a possible association.DGAT1基因3'非翻译区的新型单核苷酸多态性和插入缺失多态性:电子分析及可能的关联
Mol Biol Rep. 2014 Jul;41(7):4555-63. doi: 10.1007/s11033-014-3326-z. Epub 2014 Mar 28.

本文引用的文献

1
Critical association of ncRNA with introns.非编码 RNA 与内含子的关键关联。
Nucleic Acids Res. 2011 Mar;39(6):2357-66. doi: 10.1093/nar/gkq1080. Epub 2010 Nov 10.
2
HSP90 protein stabilizes unloaded argonaute complexes and microscopic P-bodies in human cells.热休克蛋白 90 使空载的 Argonaute 复合物和人细胞中的微观 P 体稳定。
Mol Biol Cell. 2010 May 1;21(9):1462-9. doi: 10.1091/mbc.e09-10-0885. Epub 2010 Mar 17.
3
Causes and consequences of microRNA dysregulation in cancer.癌症中微小RNA失调的原因及后果。
Nat Rev Genet. 2009 Oct;10(10):704-14. doi: 10.1038/nrg2634.
4
The DEAD-box protein p72 regulates ERalpha-/oestrogen-dependent transcription and cell growth, and is associated with improved survival in ERalpha-positive breast cancer.DEAD盒蛋白p72调节雌激素受体α/雌激素依赖性转录和细胞生长,并与雌激素受体α阳性乳腺癌患者的生存率提高相关。
Oncogene. 2009 Nov 19;28(46):4053-64. doi: 10.1038/onc.2009.261. Epub 2009 Aug 31.
5
Limitations and possibilities of small RNA digital gene expression profiling.小RNA数字基因表达谱分析的局限性与可能性
Nat Methods. 2009 Jul;6(7):474-6. doi: 10.1038/nmeth0709-474.
6
Biogenesis of small RNAs in animals.动物中小RNA的生物合成
Nat Rev Mol Cell Biol. 2009 Feb;10(2):126-39. doi: 10.1038/nrm2632.
7
The RNA helicase p68 is a novel androgen receptor coactivator involved in splicing and is overexpressed in prostate cancer.RNA解旋酶p68是一种参与剪接的新型雄激素受体共激活因子,在前列腺癌中过表达。
Cancer Res. 2008 Oct 1;68(19):7938-46. doi: 10.1158/0008-5472.CAN-08-0932.
8
A multifunctional human Argonaute2-specific monoclonal antibody.一种多功能的人源 Argonaute2 特异性单克隆抗体。
RNA. 2008 Jun;14(6):1244-53. doi: 10.1261/rna.973808. Epub 2008 Apr 22.
9
The Argonaute protein family.阿贡纳乌特蛋白家族。
Genome Biol. 2008;9(2):210. doi: 10.1186/gb-2008-9-2-210. Epub 2008 Feb 26.
10
Argonaute proteins: key players in RNA silencing.Argonaute蛋白:RNA沉默的关键参与者。
Nat Rev Mol Cell Biol. 2008 Jan;9(1):22-32. doi: 10.1038/nrm2321.

一个进化上保守的、可变剪接的 p68/DDX5 DEAD-box RNA 解旋酶基因内含子编码一个新的 miRNA。

An evolutionarily conserved, alternatively spliced, intron in the p68/DDX5 DEAD-box RNA helicase gene encodes a novel miRNA.

出版信息

RNA. 2011 Apr;17(4):555-62. doi: 10.1261/rna.2591611. Epub 2011 Feb 23.

DOI:10.1261/rna.2591611
PMID:21346006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3062168/
Abstract

The DEAD-box RNA helicase p68 (DDX5) plays important roles in several cellular processes, including transcription, pre-mRNA processing, and microRNA (miRNA) processing. p68 expression is growth and developmentally regulated, and alterations in p68 expression and/or function have been implicated in tumor development. The p68 gene encodes an evolutionarily conserved, alternatively spliced, intron the function of which has to date remained unclear. Although the intron-containing p68 RNA does not appear to yield an alternative p68 protein, it is differentially expressed in cell lines and tissues, indicating regulation of expression. Here we show that the p68 conserved intron encodes a novel putative miRNA, suggesting a previously unknown possible regulatory function for the p68 intron. We show that this miRNA (referred to as p68 miRNA) is processed from the intron via the canonical miRNA-processing pathway and that it associates with the Argonaute protein Ago2. Finally we show that the p68 miRNA suppresses an mRNA bearing complementary target sequences, suggesting that it is functional. These findings suggest a novel mechanism by which alterations in p68 expression may impact on the cell.

摘要

DEAD -box RNA 解旋酶 p68(DDX5)在多个细胞过程中发挥重要作用,包括转录、前体 mRNA 加工和 microRNA(miRNA)加工。p68 的表达受到生长和发育的调控,p68 表达和/或功能的改变与肿瘤的发生有关。p68 基因编码一个进化上保守的、可变剪接的内含子,其功能迄今仍不清楚。尽管含有内含子的 p68 RNA 似乎不会产生替代的 p68 蛋白,但它在细胞系和组织中的表达存在差异,表明其受到调控。在这里,我们表明 p68 保守内含子编码一种新的潜在 miRNA,这表明 p68 内含子具有以前未知的可能的调节功能。我们表明,这种 miRNA(称为 p68 miRNA)通过经典的 miRNA 加工途径从内含子中加工而来,并与 Argonaute 蛋白 Ago2 结合。最后,我们表明 p68 miRNA 抑制具有互补靶序列的 mRNA,表明其具有功能。这些发现表明,p68 表达的改变可能通过一种新的机制影响细胞。