Target intelligence / Profile preview

Twinfilin actin binding protein 2 mRNA 3' untranslated region (TWF2 mRNA 3'UTR)

Target
TWF2 mRNA 3'UTR
Molecular classification
RNA regulatory element, Other
01

Overview

The TWF2 mRNA 3'UTR is a critical non-coding regulatory segment located at the 3' end of the transcript for Twinfilin actin binding protein 2 (TWF2). This region is essential for the post-transcriptional control of TWF2, an actin-sequestering protein that plays a vital role in modulating the cytoskeleton and cell morphology. The 3'UTR contains highly conserved binding sites for muscle-specific microRNAs, most notably miR-1 and miR-133, which act to suppress TWF2 expression in healthy cardiac and skeletal muscle tissues (PubMed: 17406499). In pathological conditions such as cardiac hypertrophy, the downregulation of miR-1 leads to a loss of inhibitory control over the TWF2 3'UTR, resulting in the overexpression of TWF2 protein and subsequent maladaptive actin remodeling. This regulatory axis has also been implicated in cancer progression, where TWF2 levels influence cell motility and metastasis. Consequently, the TWF2 mRNA 3'UTR is a significant target for experimental RNA-based therapies, such as miRNA mimics, designed to restore normal protein levels and mitigate disease progression in cardiovascular and oncological contexts.

Other names
PTK9L mRNA 3'UTRTwinfilin-2 mRNA 3'UTRA6-related protein mRNA 3'UTR3' untranslated region of TWF2
02

Mechanism of action

The 3'UTR serves as a physical binding site for regulatory microRNAs (miRNAs) or antisense oligonucleotides (ASOs). Binding of these agents, particularly miR-1, to the TWF2 3'UTR recruits the RNA-induced silencing complex (RISC), which leads to the degradation of the TWF2 mRNA or the inhibition of its translation into protein (Care et al., 2007, Nature Medicine).

03

Biological functions

Post-transcriptional regulationActin cytoskeleton organizationmRNA stability regulationCellular component organization
04

Disease associations

Cardiac hypertrophyCancerCardiovascular diseaseMuscle development disorders
05

Safety considerations

Off-target silencing of other genes sharing similar seed sequencesPotential for innate immune activation by exogenous RNA moleculesChallenges in tissue-specific delivery of RNA-targeted therapeutics
06

Interacting drugs

miR-1 mimic (experimental)

1 more in the full profile.

07

Biomarkers

TWF2 mRNA expression levelsTWF2 protein levelsmiR-1 expression levels

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