Cited by 20RNA Research and SplicingRNA regulation and diseaseRNA and protein synthesis mechanisms

Ectopic expression of Drosophila ELAV and human HuD in Drosophila wing disc cells reveals functional distinctions and similarities

Toba, Gakuta, Qui, Jan, Koushika, Sandhya P., White, Kalpana·2002·Journal of Cell Science

Abstract

Drosophila ELAV and human HuD are two neuronal RNA binding proteins that show remarkable sequence homology, yet differ in their respective documented roles in post-transcriptional regulation. ELAV regulates neural-specific alternative splicing of specific transcripts, and HuD stabilizes specific mRNAs that are otherwise unstable due to AU-rich elements (AREs) in their 3' untranslated region (UTR). AREs are major determinants of transcript stability in mammalian cells. The role of each of these proteins was investigated and compared, by ectopically expressing them in Drosophila imaginal wing disc cells, which lack endogenous expression of either protein. The effect of the ectopic expression of ELAV and HuD was assessed on two sets of green fluorescent protein reporter transgenes, which were all driven with a broadly expressing promoter. Each set consisted of three reporter transgenes: (1) with an uninterrupted open reading frame (ORF); (2) with a constitutively spliced intron inserted into the ORF; and (3) with the intron nASI whose splicing is regulated in neurons by ELAV, inserted into the ORF. The two sets differed from each other only in their 3'UTR: Heat-shock-protein-70Ab (Hsp70Ab) trailer with ARE-like characteristics or Actin 5C (Act5C) trailer. Our results show that: (1) both ectopically expressed ELAV and HuD can enhance expression of transgenes with the Hsp70Ab 3'UTR, but not of transgenes with Act5C 3'UTR; (2) this enhancement is accompanied by an increase in mRNA…

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Registry

Crossref · 10.1242/jcs.115.11.2413

Cites

1 of 1 references verified0 citation errors · 0 not checkable

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  • The presence of an AUUUA sequence is not always sufficient for HuD binding, indicating that HuD displays preference for specific ARE motifs.

    “However, it is important to point out that the presence of an AUUUA sequence is not always sufficient for HuD binding, indicating that HuD displays preference for specific ARE motifs (Toba et al. 2002).”

Authors
Toba, G., Qui, J., Koushika, S. P., & White, K.
Affiliations
  • Brandeis University (US)
  • Washington University in St. Louis (US)
Corresponding author
White, Kalpana
Venue
Journal of Cell Science
Published
2002-06-01
Volume
115
Issue
11
Pages
2413-2421
ISSN
  • 0021-9533 (ISSN-L)
  • 1477-9137
OpenAlex
W2203796204
Cited by
20
References
1
Citations by year
2021: 3 · 2020: 1 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 1
FWCI
0.46
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Cell Science (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ns036179-05)
  • National Institute of General Medical Sciences (P01GM033205, GM-33205)
  • National Institute of Neurological Disorders and Stroke (NS36179, T32NS007292)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords
ELAV, HUD, RNA-binding proteins, AU-rich elements, mRNA stability, alternative splicing, post-transcriptional regulation, 3' untranslated region, ectopic expression, subcellular localization
MeSH terms
ELAV-Like Protein 4, Animals, Cell Differentiation, Choristoma, Drosophila melanogaster, Female, Genes, Regulator, Humans, Introns, Larva, Luminescent Proteins, Male, Nerve Tissue Proteins, Nervous System, Neurons, Ribonucleoproteins, RNA, RNA Splicing, Wings, Animal, RNA-Binding Proteins, Genes, Reporter, Gene Expression Regulation, Developmental, HSP70 Heat-Shock Proteins, 3' Untranslated Regions, Animals, Genetically Modified, Green Fluorescent Proteins, ELAV Proteins

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