ArticlePlant molecular biology1994
Addition of A- and U-rich sequence increases the splicing efficiency of a deleted form of a maize intron.
Article in Plant molecular biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.
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Who cites it
37 citing papers in PubMed, 72 citations in OpenAlex.
- Genomic basis underlying alternative transcripts-mediated drought tolerance in maize.Genome biology · 2026Article
- Sequence-dependent and -independent effects of intron-mediated enhancement learned from thousands of random introns.Nucleic acids research · 2025Article
- Maize splicing-mediated mRNA surveillance impeded by sugarcane mosaic virus-coded pathogenic protein NIa-Pro.Science advances · 2024Article
- Phylogenetic comparison and splice site conservation of eukaryotic U1 snRNP-specific U1-70K gene family.Scientific reports · 2021Article
- Intron sequences that stimulate gene expression in Arabidopsis.Plant molecular biology · 2016Article
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- Spurious polyadenylation of Norovirus Narita 104 capsid protein mRNA in transgenic plants.Plant molecular biology · 2011Article
- Evidence for a DNA-Based Mechanism of Intron-Mediated Enhancement.Frontiers in plant science · 2011Article
- The leader intron of AtMHX can elicit, in the absence of splicing, low-level intron-mediated enhancement that depends on the internal intron sequence.BMC plant biology · 2010Article
- Transcriptional and post-transcriptional enhancement of gene expression by the 5' UTR intron of rice rubi3 gene in transgenic rice cells.Molecular genetics and genomics : MGG · 2008Article
- Novel plant transformation vectors containing the superpromoter.Plant physiology · 2007Article
- Effect of 5'UTR introns on gene expression in Arabidopsis thaliana.BMC genomics · 2006Article
- Article
- Two genes encoding protein phosphatase 2A catalytic subunits are differentially expressed in rice.Plant molecular biology · 2003Article
- Requirements for intron-mediated enhancement of gene expression in Arabidopsis.RNA (New York, N.Y.) · 2002Article
- Splicing of the maize Sh1 first intron is essential for enhancement of gene expression, and a T-rich motif increases expression without affecting splicing.Plant physiology · 2002Article
- Mutational analysis of a plant branchpoint and polypyrimidine tract required for constitutive splicing of a mini-exon.RNA (New York, N.Y.) · 2002Article
- Tissue-preferential expression of a rice alpha-tubulin gene, OsTubA1, mediated by the first intron.Plant physiology · 2000Article
- UBP1, a novel hnRNP-like protein that functions at multiple steps of higher plant nuclear pre-mRNA maturation.The EMBO journal · 2000Article
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2 authors at 1 institution in 1 country.
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Abstract
Plant introns are generally short (< 200 nt) and AU-rich, and an elevated AU content is necessary for efficient splicing. Further, an intron in some plant genes enhances gene expression by a post-transcriptional mechanism that results in an increase of cytoplasmic mRNA. The specific intron features responsible for efficient splicing and enhancement are not well characterized in plants. Internal deletions of up to 80% of two maize introns, Adh1 intron 1 and maize actin 3, indicate that large segments of these introns are dispensable for normal function. However, extensive deletion (> 75%) of Adh1 intron 1 diminishes both intron enhancement and splicing efficiency. This finding suggests that there are internal sequence motifs required for intron function, and that these motifs are redundant. We attempted to repair a deletion-impaired Adh1 intron 1 variant by adding back either oligomers of defined sequence content or fragments of maize internal intron sequence. The addition of AU-rich oligomers improved splicing efficiency and in one example, a U-rich oligomer activated a cryptic 3' splice acceptor. We also found that replacing the region proximal to the Adh1 intron 1 3' acceptor with U-rich sequence improved splicing. We found that adding G- and C-rich oligomers did not improve intron function, but a C-rich oligomer activated a cryptic 3' acceptor. The addition of internal intron sequence to an impaired intron improved splicing, and in one case, resulted in the activation of a cryptic 3' acceptor. We present evidence that U-rich sequence immediately upstream of the 3' splice junction increases splicing efficiency and contributes to, but does not uniquely specify, 3' acceptor AG choice.
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