Gene organization and chromosome location of the neural-specific RNA binding protein Elavl4
Abstract
We have isolated the gene that encodes the neural-specific RNA binding protein HuD in the mouse (Elavl4), and have mapped its location to the mid-distal region of chromosome 4, close to the neurological mutant clasper. The coding region of the Elavl4 gene covers approximately 44 kb; the first two RNA binding domains (RBDs) that are homologous to the two RBDs found in the Drosophila sex-lethal gene are each encoded in two exons, whereas the third RBD is encoded in a single exon. Elavl4 mRNAs are alternatively spliced in the region between RBDs 2 and 3 due to the variable use of two micro-exons, and RNase protection analysis indicates that two of four possible splice variants are the predominant isoforms expressed in the central nervous system. The high degree of sequence conservation between the Hu proteins suggests that the exon organization of all the Hu protein genes will be similar, if not identical, to the Elavl4 gene.
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In the HuD gene locus, E2 and E3, E4 and E5, and E8 encode the three RRMs, whereas the alternatively spliced E6 and E7 encode the linker region.
“In the HuD gene locus, E2 and E3, E4 and E5, and E8 encode the three RRMs, respectively, whereas the alternatively spliced E6 and E7 encode the linker region (Inman et al. 1998).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
The HuD gene is well conserved among higher vertebrates and is located on chromosome 1 in humans and chromosome 4 in mice.
“Overall, the HuD gene is well conserved among higher vertebrates and is located on chromosome 1 in humans and chromosome 4 in mice (Fig. 1A).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
The human and mouse HuD gene spans approximately 146 kb of DNA and is divided into seven coding exons (E2 to E8) that encompass approximately 44 kb of DNA.
“The human and mouse HuD gene spans ∼146 kb of DNA and is divided into seven coding exons (E2 to E8) that encompass ∼44 kb of DNA (Sekido et al. 1994; Inman et al. 1998).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
HuD pre-mRNA is subjected to alternative splicing of exons 6 and 7, resulting in three additional transcript isoforms (HuD, HuDmex, and HuDpro), two of which are predominantly expressed in the postnatal mouse brain (HuD and HuDpro).
“In addition to the 5′ end, HuD pre-mRNA is subjected to alternative splicing of exons (E) 6 and 7, resulting in three additional transcript isoforms (HuD, HuDmex, and HuDpro) (Fig. 1B,C), two of which are predominantly expressed in the postnatal mouse brain (HuD and HuDpro) (Inman et al. 1998).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
Previous studies, along with data from our laboratory, revealed eight HuD E1 variants, indicating the existence of at least eight different 5′ UTRs, with most containing an in-frame translation start site.
“As mentioned above, previous studies, along with data from our laboratory, revealed eight HuD E1 variants, indicating the existence of at least eight different 5′ UTRs (Fig. 1A,B), with most containing an in-frame translation start site (Abe et al. 1994; Inman et al. 1998; Bronicki et al. 2012).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
A previous study suggested that at least three HuD E1 variants exist, pointing to the potential presence of multiple promoters.
“As discussed above, a previous study suggested that at least three HuD E1 variants exist, pointing to the potential presence of multiple promoters (Inman et al. 1998).”
From Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction (2013) · cites this paper as Inman et al. 1998
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Bronicki, L. M., & Jasmin, B. J. (2013) · RNA · doi:10.1261/rna.039164.113 · Cited by 126 · see citing works
Computational discovery of internal micro-exons
Volfovsky, N., Haas, B. J., & Salzberg, S. L. (2003) · Genome Research · doi:10.1101/gr.677503 · Cited by 87 · see citing works
RNA–Binding Protein HuD as a Versatile Factor in Neuronal and Non–Neuronal Systems
Jung, M., & Lee, E. K. (2021) · Biology · doi:10.3390/biology10050361 · Cited by 39 · see citing works
- Authors
- Inman, M. V., Levy, S., Mock, B. A., & Owens, G. C.
- Affiliations
- University of Colorado Health (US)
- University of Colorado Boulder (US)
- National Institutes of Health (US)
- Corresponding author
- Owens, Geoffrey C
- ORCID
- Mock, Beverly A
- Venue
- Gene
- Publisher
- Elsevier BV
- Published
- 1998-02
- Volume
- 208
- Issue
- 2
- Pages
- 139-145
- ISSN
- 0378-1119 (ISSN-L)
- OpenAlex
- W2031247595
- Cited by
- 21
- References
- 3
- Citations by year
- 2026: 1 · 2025: 1 · 2021: 3 · 2014: 1 · 2013: 4 · 2012: 3
- FWCI
- 0.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Gene (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- ELAVL4, HUD, HU protein, RNA-binding proteins, gene structure, chromosome 4, claspers, alternative splicing, RNA-binding domain, splice variants, central nervous system, exon organization, sequence conservation
- MeSH terms
- ELAV-Like Protein 4, Aging, Animals, Base Sequence, Brain, Chromosome Mapping, Drosophila, Exons, Genetic Markers, Introns, Mice, Neurologic Mutants, Molecular Sequence Data, Nerve Tissue Proteins, Oligodeoxyribonucleotides, RNA, Messenger, Transcription, Genetic, Genetic Variation, Restriction Mapping, RNA-Binding Proteins, Alternative Splicing, Protein Structure, Secondary, Gene Expression Regulation, Developmental, Drosophila Proteins, Mice, ELAV Proteins
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