Defining a neuron: neuronal ELAV proteins
Open accessAbstract
Neuronal cells strongly depend on the control exerted by RNA-binding proteins (RBPs) on gene expression for the establishment and maintenance of their phenotype. Neuronal ELAV (nELAV) proteins are RBPs able to influence virtually every aspect of the postsynthesis fate of bound mRNAs, from polyadenylation, alternative splicing and nuclear export to cytoplasmic localization, stability and translation. They enhance gene expression through the last two, best documented activities, increasing mRNA half-life and promoting protein synthesis by a still-unknown molecular mechanism. Developmentally, nELAV proteins have been shown to act as inducers of the transition between neural stem/progenitor cells and differentiation-committed cells, also assisting these neuroblasts in the completion of their maturation program. In brain physiology, they are also the first RBPs demonstrated to have a pivotal role in memory, where they probably control mRNA availability for translation in subcellular domains, thereby providing a biochemical means for selective increase in synaptic strength.
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There are a few known AUBPs that enhance mRNA stability, with Hu proteins being the most notable.
“Nevertheless, there are a few known AUBPs that enhance mRNA stability, with Hu proteins being the most notable (Brennan and Steitz 2001; Hinman and Lou 2008; Pascale et al. 2008).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Pascale et al. 2008
ELAVL1 is widely expressed in non-neuronal tissues.
“ELAVL1 (also known as HuR or HuA) is widely expressed in non-neuronal tissues”
From The neurogenetics of alternative splicing (2016) · cites this paper as [120]
ELAVL2, ELAVL3 and ELAVL4 show neuronal-specific expression.
“whereas ELAVL2 (also known as HuB), ELAVL3 (also known as HuC) and ELAVL4 (also known as HuD) show neuronal-specific expression”
From The neurogenetics of alternative splicing (2016) · cites this paper as [120]
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References 127 · Cited by 158
- Authors
- Pascale, A., Amadio, M., & Quattrone, A.
- Affiliations
- University of Pavia (IT)
- University of Trento (IT)
- Corresponding author
- Pascale, A.
- Quattrone, A.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2007-10-12
- Volume
- 65
- Issue
- 1
- Pages
- 128-140
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11131659
- OpenAlex
- W2042713128
- Cited by
- 158
- References
- 127
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 14 · 2023: 3 · 2022: 6 · 2021: 4 · 2020: 16 · 2019: 4 · 2018: 8 · 2017: 4 · 2016: 6 · 2015: 9 · 2014: 9 · 2013: 15 · 2012: 9
- FWCI
- 3.44
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- RNA-binding proteins, mRNA stability, translational regulation, alternative splicing, polyadenylation, nuclear export, mRNA localization, neural stem/progenitor cells, neuronal differentiation, memory, synaptic plasticity
- MeSH terms
- Animals, Cell Differentiation, Humans, Memory, Neuronal Plasticity, Neurons, RNA Stability, ELAV Proteins
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