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The role of microRNA-221 and microRNA-222 in androgen-independent prostate cancer cell lines.微小RNA - 221和微小RNA - 222在雄激素非依赖性前列腺癌细胞系中的作用。
Cancer Res. 2009 Apr 15;69(8):3356-63. doi: 10.1158/0008-5472.CAN-08-4112. Epub 2009 Apr 7.
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The promoter of the pri-miR-375 gene directs expression selectively to the endocrine pancreas.pri-miR-375基因的启动子将表达选择性地导向内分泌胰腺。
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MicroRNA-21 is up-regulated in allergic airway inflammation and regulates IL-12p35 expression.微小RNA-21在过敏性气道炎症中上调并调节白细胞介素-12p35的表达。
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MicroRNA-101, down-regulated in hepatocellular carcinoma, promotes apoptosis and suppresses tumorigenicity.微小RNA-101在肝细胞癌中表达下调,可促进细胞凋亡并抑制肿瘤发生。
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内含子 miRNA 启动子的结构与活性。

Structure and activity of putative intronic miRNA promoters.

机构信息

Department of Internal Medicine, University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

RNA. 2010 Mar;16(3):495-505. doi: 10.1261/rna.1731910. Epub 2010 Jan 14.

DOI:10.1261/rna.1731910
PMID:20075166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2822915/
Abstract

MicroRNAs (miRNAs) are RNA sequences of approximately 22 nucleotides that mediate post-transcriptional regulation of specific mRNAs. miRNA sequences are dispersed throughout the genome and are classified as intergenic (between genes) or intronic (embedded into a gene). Intergenic miRNAs are expressed by their own promoter, and until recently, it was supposed that intronic miRNAs are transcribed from their host gene. Here, we performed a genomic analysis of currently known intronic miRNA regions and observed that approximately 35% of intronic miRNAs have upstream regulatory elements consistent with promoter function. Among all intronic miRNAs, 30% have associated Pol II regulatory elements, including transcription start sites, CpG islands, expression sequence tags, and conserved transcription factor binding sites, while 5% contain RNA Pol III regulatory elements (A/B box sequences). We cloned intronic regions encompassing miRNAs and their upstream Pol II (miR-107, miR-126, miR-208b, miR-548f-2, miR-569, and miR-590) or Pol III (miR-566 and miR-128-2) sequences into a promoterless plasmid, and confirmed that miRNA expression occurs independent of host gene transcription. For miR-128-2, a miRNA overexpressed in acute lymphoblastic leukemia, ChIP analysis suggests dual regulation by both intronic (Pol III) and host gene (Pol II) promoters. These data support complex regulation of intronic miRNA expression, and have relevance to disregulation in disease settings.

摘要

微小 RNA(miRNAs)是大约 22 个核苷酸的 RNA 序列,介导特定 mRNAs 的转录后调控。miRNA 序列分散在基因组中,分为基因间(在基因之间)或内含子(嵌入基因内)。基因间 miRNA 由其自身的启动子表达,直到最近,人们还认为内含子 miRNA 是从其宿主基因转录而来的。在这里,我们对目前已知的内含子 miRNA 区域进行了基因组分析,观察到大约 35%的内含子 miRNA 具有与启动子功能一致的上游调节元件。在所有内含子 miRNA 中,有 30%具有相关的 Pol II 调节元件,包括转录起始位点、CpG 岛、表达序列标签和保守转录因子结合位点,而 5%含有 RNA Pol III 调节元件(A/B 框序列)。我们克隆了包含 miRNA 及其上游 Pol II(miR-107、miR-126、miR-208b、miR-548f-2、miR-569 和 miR-590)或 Pol III(miR-566 和 miR-128-2)序列的内含子区域,将其插入无启动子质粒中,并证实 miRNA 表达与宿主基因转录无关。对于在急性淋巴细胞白血病中过度表达的 miRNA-128-2,ChIP 分析表明其受到内含子(Pol III)和宿主基因(Pol II)启动子的双重调节。这些数据支持内含子 miRNA 表达的复杂调控,并与疾病状态下的失调有关。