» Articles » PMID: 20075166

Structure and Activity of Putative Intronic MiRNA Promoters

Overview
Journal RNA
Specialty Molecular Biology
Date 2010 Jan 16
PMID 20075166
Citations 195
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

MicroRNA profiling identifies VHL/HIF-2α dependent miR-2355-5p as a key modulator of clear cell Renal cell carcinoma tumor growth.

Page P, Dastous S, Richard P, Pavic M, Nishimura T, Riazalhosseini Y Cancer Cell Int. 2025; 25(1):71.

PMID: 40016765 PMC: 11869434. DOI: 10.1186/s12935-025-03711-3.


miR-198 targets : implications for oral squamous cell carcinoma pathogenesis.

Kaushik P, Mishra R, Gopal C, Kumar A Front Oncol. 2024; 14:1485802.

PMID: 39697236 PMC: 11652479. DOI: 10.3389/fonc.2024.1485802.


Next-Cell Hypothesis: Mechanism of Obesity-Associated Carcinogenesis.

Engin A, Engin A Adv Exp Med Biol. 2024; 1460:727-766.

PMID: 39287871 DOI: 10.1007/978-3-031-63657-8_25.


MicroRNAs as Epigenetic Regulators of Obesity.

Engin A, Engin A Adv Exp Med Biol. 2024; 1460:595-627.

PMID: 39287866 DOI: 10.1007/978-3-031-63657-8_20.


Expression and Functional Analysis of Immuno-Micro-RNAs mir-146a and mir-326 in Colorectal Cancer.

Farc O, Budisan L, Zaharie F, Taulean R, Valean D, Talvan E Curr Issues Mol Biol. 2024; 46(7):7065-7085.

PMID: 39057062 PMC: 11276483. DOI: 10.3390/cimb46070421.


References
1.
Morlando M, Ballarino M, Gromak N, Pagano F, Bozzoni I, Proudfoot N . Primary microRNA transcripts are processed co-transcriptionally. Nat Struct Mol Biol. 2009; 15(9):902-9. PMC: 6952270. DOI: 10.1038/nsmb.1475. View

2.
Gervais F, Singaraja R, Xanthoudakis S, Gutekunst C, Leavitt B, Metzler M . Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi. Nat Cell Biol. 2002; 4(2):95-105. DOI: 10.1038/ncb735. View

3.
Avnit-Sagi T, Kantorovich L, Kredo-Russo S, Hornstein E, Walker M . The promoter of the pri-miR-375 gene directs expression selectively to the endocrine pancreas. PLoS One. 2009; 4(4):e5033. PMC: 2660411. DOI: 10.1371/journal.pone.0005033. View

4.
Kim Y, Kim V . Processing of intronic microRNAs. EMBO J. 2007; 26(3):775-83. PMC: 1794378. DOI: 10.1038/sj.emboj.7601512. View

5.
Naykova T, Kondrakhin Y, Rogozin I, Voevoda M, Yudin N, Romaschenko A . Concerted changes in the nucleotide sequences of the intragenic promoter regions of eukaryotic genes for tRNAs of all specificities. J Mol Evol. 2004; 57(5):520-32. DOI: 10.1007/s00239-003-2504-8. View