Literature DB >> 11959978

Stop codons affect 5' splice site selection by surveillance of splicing.

Binghui Li1, Chaim Wachtel, Elana Miriami, Galit Yahalom, Gilgi Friedlander, Gil Sharon, Ruth Sperling, Joseph Sperling.   

Abstract

Pre-mRNA splicing involves recognition of a consensus sequence at the 5' splice site (SS). However, only some of the many potential sites that conform to the consensus are true ones, whereas the majority remain silent and are not normally used for splicing. We noticed that in most cases the utilization of such a latent intronic 5' SS for splicing would introduce an in-frame stop codon into the resultant mRNA. This finding suggested a link between SS selection and maintenance of an ORF within the mRNA. Here we tested this idea by analyzing the splicing of pre-mRNAs in which in-frame stop codons upstream of a latent 5' SS were mutated. We found that splicing with the latent site is indeed activated by such mutations. Our findings predict the existence of a checking mechanism, as a component of the nuclear pre-mRNA splicing machine, to ensure the maintenance of an ORF. This notion is highly important for accurate gene expression, as perturbations that would lead to splicing at these latent sites are expected to introduce in-frame stop codons into the majority of mRNAs.

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Year:  2002        PMID: 11959978      PMCID: PMC122760          DOI: 10.1073/pnas.082095299

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  39 in total

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Review 3.  RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer.

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5.  Proofreading and aminoacylation of tRNAs before export from the nucleus.

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6.  The association of nonsense mutation with exon-skipping in hprt mRNA of Chinese hamster ovary cells results from an artifact of RT-PCR.

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7.  Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line.

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8.  Multiple distinct splicing enhancers in the protein-coding sequences of a constitutively spliced pre-mRNA.

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10.  Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm.

Authors:  J Zhang; X Sun; Y Qian; L E Maquat
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  26 in total

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Review 4.  Latent splice sites and stop codons revisited.

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Review 5.  Nuclear translation: what is the evidence?

Authors:  James E Dahlberg; Elsebet Lund; Elizabeth B Goodwin
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6.  Stop codon-mediated suppression of splicing is a novel nuclear scanning mechanism not affected by elements of protein synthesis and NMD.

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7.  A potential role for initiator-tRNA in pre-mRNA splicing regulation.

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8.  Alternative splicing induced by nonsense mutations in the immunoglobulin mu VDJ exon is independent of truncation of the open reading frame.

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9.  Nonsense-associated alternative splicing of T-cell receptor beta genes: no evidence for frame dependence.

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Journal:  RNA       Date:  2004-12-21       Impact factor: 4.942

10.  Loss of exon identity is a common mechanism of human inherited disease.

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