Target intelligence / Profile preview

Iron-responsive element in the 5'-untranslated region of TAR DNA-binding protein 43 mRNA (TDP-43 5'-UTR IRE)

Target
TDP-43 5'-UTR IRE
Molecular classification
RNA, Regulatory element, Non-coding RNA element
01

Overview

The Iron-responsive element (IRE) in the 5'-untranslated region (UTR) of TAR DNA-binding protein 43 (TDP-43) mRNA is a conserved RNA stem-loop structure that regulates the translation of TDP-43 in response to cellular iron levels (Annovis Bio, 2023). This regulatory element serves as a binding site for Iron Regulatory Proteins (IRP1 and IRP2); when iron levels are low, IRPs bind to the IRE and sterically hinder the assembly of the translation initiation complex, thereby reducing TDP-43 protein synthesis (Journal of Neurochemistry, 2021). In neurodegenerative diseases like Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD), the pathological accumulation and aggregation of TDP-43 are central to disease progression (PubMed, 2022). The small molecule Buntanetap (formerly Posiphen) targets this IRE to enhance translational repression, effectively lowering the production of neurotoxic TDP-43 (Annovis Bio, 2022). By modulating this RNA-protein interaction, researchers aim to restore proteostasis and mitigate the neurodegenerative process, although care must be taken to maintain the essential physiological functions of TDP-43 in RNA processing (Frontiers in Molecular Neuroscience, 2020).

Other names
TARDBP 5'-UTR IRETDP-43 mRNA iron-responsive elementIron-responsive element of TAR DNA-binding protein 43TDP-43 IRE
02

Mechanism of action

Translational inhibition through the modulation of Iron Regulatory Protein (IRP) binding to the 5'-UTR IRE stem-loop

03

Biological functions

Post-transcriptional regulationIron homeostasisTranslation regulationmRNA stability
04

Disease associations

Amyotrophic lateral sclerosisFrontotemporal lobar degenerationAlzheimer's diseaseNeurodegenerative disease
05

Safety considerations

Potential for systemic iron metabolism disruptionOff-target inhibition of essential IRE-containing proteins such as ferritin or transferrin receptorToxicity resulting from excessive reduction of physiological TDP-43 levelsPotential for unintended effects on RNA splicing regulated by TDP-43
06

Interacting drugs

Buntanetap

1 more in the full profile.

07

Biomarkers

TDP-43 protein levels in cerebrospinal fluidNeurofilament light chain (NfL)Brain iron concentration via MRITDP-43 levels in plasma

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