» Articles » PMID: 26631377

The MiR-302/367 Cluster: a Comprehensive Update on Its Evolution and Functions

Overview
Journal Open Biol
Date 2015 Dec 4
PMID 26631377
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

microRNAs are a subclass of small non-coding RNAs that fine-tune the regulation of gene expression at the post-transcriptional level. The miR-302/367 cluster, generally consisting of five members, miR-367, miR-302d, miR-302a, miR-302c and miR-302b, is ubiquitously distributed in vertebrates and occupies an intragenic cluster located in the gene La-related protein 7 (LARP7). The cluster was demonstrated to play an important role in diverse biological processes, such as the pluripotency of human embryonic stem cells (hESCs), self-renewal and reprogramming. This paper provides an overview of the mir-302/367 cluster, discusses our current understanding of the cluster's evolutionary history and transcriptional regulation and reviews the literature surrounding the cluster's roles in cell cycle regulation, epigenetic regulation and different cellular signalling pathways.

Citing Articles

Targeting Invasion: The Role of MMP-2 and MMP-9 Inhibition in Colorectal Cancer Therapy.

Shoari A, Ashja Ardalan A, Dimesa A, Coban M Biomolecules. 2025; 15(1).

PMID: 39858430 PMC: 11762759. DOI: 10.3390/biom15010035.


MicroRNAs in Genitourinary Malignancies: An Exciting Frontier of Cancer Diagnostics and Therapeutics.

Kathuria-Prakash N, Dave P, Garcia L, Brown P, Drakaki A Int J Mol Sci. 2024; 25(17).

PMID: 39273446 PMC: 11394927. DOI: 10.3390/ijms25179499.


-amplifying RNA expressing functional miRNA mediates target gene suppression and simultaneous transgene expression.

Yildiz A, Hasani A, Hempel T, Kohl N, Beicht A, Becker R Mol Ther Nucleic Acids. 2024; 35(2):102162.

PMID: 38545619 PMC: 10965815. DOI: 10.1016/j.omtn.2024.102162.


Dysregulated expression of miR‑367 in disease development and its prospects as a therapeutic target and diagnostic biomarker (Review).

Muniandy S, Few L, Khoo B, Hassan S, Yvonne-Tee G, See Too W Biomed Rep. 2023; 19(6):91.

PMID: 37901877 PMC: 10603372. DOI: 10.3892/br.2023.1673.


Cardiac microRNAs: diagnostic and therapeutic potential.

Kablak-Ziembicka A, Badacz R, Okarski M, Wawak M, Przewlocki T, Podolec J Arch Med Sci. 2023; 19(5):1360-1381.

PMID: 37732050 PMC: 10507763. DOI: 10.5114/aoms/169775.


References
1.
Kumar M, Patel N, Nicholson A, Kalen A, Sarsour E, Goswami P . Reactive oxygen species mediate microRNA-302 regulation of AT-rich interacting domain 4a and C-C motif ligand 5 expression during transitions between quiescence and proliferation. Free Radic Biol Med. 2012; 53(4):974-82. PMC: 3418417. DOI: 10.1016/j.freeradbiomed.2012.06.019. View

2.
Gerstein M, Kundaje A, Hariharan M, Landt S, Yan K, Cheng C . Architecture of the human regulatory network derived from ENCODE data. Nature. 2012; 489(7414):91-100. PMC: 4154057. DOI: 10.1038/nature11245. View

3.
Ambros V . A hierarchy of regulatory genes controls a larva-to-adult developmental switch in C. elegans. Cell. 1989; 57(1):49-57. DOI: 10.1016/0092-8674(89)90171-2. View

4.
Hu W, Zhao J, Pei G . Activation of aryl hydrocarbon receptor (ahr) by tranilast, an anti-allergy drug, promotes miR-302 expression and cell reprogramming. J Biol Chem. 2013; 288(32):22972-84. PMC: 3753054. DOI: 10.1074/jbc.M113.475624. View

5.
Wheeler B, Heimberg A, Moy V, Sperling E, Holstein T, Heber S . The deep evolution of metazoan microRNAs. Evol Dev. 2009; 11(1):50-68. DOI: 10.1111/j.1525-142X.2008.00302.x. View