Related Experiment Video
Updated: May 9, 2026

06:35
A Scalable, Cell-Based Method for the Functional Assessment of Ube3a Variants
Published on: October 10, 2022
Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction
Lucas M Bronicki1, Bernard J Jasmin
1Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Summary
The RNA-binding protein HuD is crucial for neuronal gene expression, regulating mRNA processing, stability, and translation. This review details HuD
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Precise spatiotemporal gene expression control is vital in neurons, relying on messenger RNA (mRNA) processing and abundance regulation.
- Trans-acting factors, including RNA-binding proteins (RBPs) and micro-RNAs (miRs), govern mRNA metabolism by binding to cis-acting elements.
- The Hu/ELAV-like family member HuD is a well-characterized neuronal RBP influencing multiple mRNA metabolism aspects.
Purpose of the Study:
- To provide a comprehensive overview of HuD expression and function within the nervous system.
- To elucidate the molecular mechanisms controlling HuD's localization, abundance, and activity in neurons.
Main Methods:
- This review synthesizes existing literature on HuD's role in neuronal gene regulation.
- Analysis of studies investigating HuD's impact on mRNA processing, stability, and translation.
- Examination of research on HuD's involvement in neuronal development, function, plasticity, and disease.
Main Results:
- HuD regulates the fate of numerous neuronal mRNAs, impacting diverse, functionally related gene groups.
- HuD is essential for neuronal development and function, playing key roles in neuronal plasticity.
- Evidence links HuD to axonal injury recovery, learning and memory, and neurological diseases.
Conclusions:
- HuD is a central regulator of neuronal mRNA metabolism, critical for neuronal health and function.
- Understanding HuD's molecular mechanisms offers insights into neuronal plasticity and disease pathogenesis.
- Further research into HuD regulation and function is warranted for therapeutic development.
Related Concept Videos
Hedgehog Signaling Pathway
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
Huntington Disease l: Introduction
Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show reduced penetrance,...
