» Articles » PMID: 32542110

Rewired Functional Regulatory Networks Among MiRNA Isoforms (isomiRs) from Let-7 and MiR-10 Gene Families in Cancer

Overview
Specialty Biotechnology
Date 2020 Jun 17
PMID 32542110
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Classical microRNA (miRNA) has been so far believed as a single sequence, but it indeed contains multiple miRNA isoforms (isomiR) with various sequences and expression patterns. It is not clear whether these diverse isomiRs have potential relationships and whether they contribute to miRNA:mRNA interactions. Here, we aimed to reveal the potential evolutionary and functional relationships of multiple isomiRs based on let-7 and miR-10 gene families that are prone to clustering together on chromosomes. Multiple isomiRs within gene families showed similar functions to their canonical miRNAs, indicating selection of the predominant sequence. IsomiRs containing novel seed regions showed increased/decreased biological function depending on whether they had more/less specific target mRNAs than their annotated seed. Few gene ontology(GO) terms and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were shared among the target genes of the annotated seeds and the novel seeds. Various let-7 isomiRs with novel seed regions may cause opposing drug responses despite the fact that they are generated from the same miRNA locus and have highly similar sequences. IsomiRs, especially the dominant isomiRs with shifted seeds, may disturb the coding-non-coding RNA regulatory network. These findings provide insight into the multiple isomiRs and isomiR-mediated control of gene expression in the pathogenesis of cancer.

Citing Articles

Selective arm-usage of pre-miR-1307 dysregulates angiogenesis and affects breast cancer aggressiveness.

Sumer O, Schelzig K, Jung J, Li X, Moros J, Schwarzmuller L BMC Biol. 2025; 23(1):25.

PMID: 39849498 PMC: 11756181. DOI: 10.1186/s12915-025-02133-x.


Genome-Wide Identification of Gene Family in and Expression Analysis at Different Postharvest Preservation Times.

Zhang Y, Peng Y, Zhang H, Gao Q, Song F, Cui X Genes (Basel). 2024; 15(7).

PMID: 39062690 PMC: 11276291. DOI: 10.3390/genes15070911.


SDF-1 and NOTCH signaling in myogenic cell differentiation: the role of miRNA10a, 425, and 5100.

Mierzejewski B, Grabowska I, Michalska Z, Zdunczyk K, Zareba F, Irhashava A Stem Cell Res Ther. 2023; 14(1):204.

PMID: 37582765 PMC: 10426160. DOI: 10.1186/s13287-023-03429-x.


A comprehensive pan-cancer analysis reveals cancer-associated robust isomiR expression landscapes in miRNA arm switching.

Guo L, Ren D, Zhang Y, Wang Q, Yu S, Xu X Mol Genet Genomics. 2023; 298(3):521-535.

PMID: 36813858 DOI: 10.1007/s00438-023-01997-4.


A comprehensive multi-omics analysis reveals molecular features associated with cancer via RNA cross-talks in the Notch signaling pathway.

Guo L, Li S, Yan X, Shen L, Xia D, Xiong Y Comput Struct Biotechnol J. 2022; 20:3972-3985.

PMID: 35950189 PMC: 9340535. DOI: 10.1016/j.csbj.2022.07.036.


References
1.
Orostica K, Verdugo R . chromPlot: visualization of genomic data in chromosomal context. Bioinformatics. 2016; 32(15):2366-8. DOI: 10.1093/bioinformatics/btw137. View

2.
Kozomara A, Birgaoanu M, Griffiths-Jones S . miRBase: from microRNA sequences to function. Nucleic Acids Res. 2018; 47(D1):D155-D162. PMC: 6323917. DOI: 10.1093/nar/gky1141. View

3.
Bhardwaj A, Singh H, Trinidad C, Albarracin C, Hunt K, Bedrosian I . The isomiR-140-3p-regulated mevalonic acid pathway as a potential target for prevention of triple negative breast cancer. Breast Cancer Res. 2018; 20(1):150. PMC: 6290546. DOI: 10.1186/s13058-018-1074-z. View

4.
Chen J, Huang Z, Seok H, Ding J, Kataoka M, Zhang Z . mir-17-92 cluster is required for and sufficient to induce cardiomyocyte proliferation in postnatal and adult hearts. Circ Res. 2013; 112(12):1557-66. PMC: 3756475. DOI: 10.1161/CIRCRESAHA.112.300658. View

5.
Manier S, Powers J, Sacco A, Glavey S, Huynh D, Reagan M . The LIN28B/let-7 axis is a novel therapeutic pathway in multiple myeloma. Leukemia. 2016; 31(4):853-860. PMC: 5382134. DOI: 10.1038/leu.2016.296. View