A perfect message: RNA surveillance and nonsense-mediated decay.
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Summary
It is suggested that mutated b-globin mRNA from a thalassemia patient was most of the available evidence can be integrated into a reported to be very low (Chang and Kan, 1979), forecommon model.
- Type
- review
- Published
- 1999-02-05
- Cited by
- 852
- References
- 20
- Access
- Open access
- OpenAlex
- https://openalex.org/W2015087800
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:9532844
Keywords
Biology, Genetics
References
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- Identifying the right stop: determining how the surveillance complex recognizes and degrades an aberrant mRNA
- Evidence that translation reinitiation abrogates nonsense‐mediated mRNA decay in mammalian cells
- An essential component of the decapping enzyme required for normal rates of mRNA turnover
- Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.
- beta 0 thalassemia, a nonsense mutation in man.
- A mutated human homologue to yeast Upf1 protein has a dominant-negative effect on the decay of nonsense-containing mRNAs in mammalian cells.
- Binary specification of nonsense codons by splicing and cytoplasmic translation
- mRNA surveillance by the Caenorhabditis elegans smg genes.
- 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.
- Nonsense surveillance in lymphocytes?
- A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance.
- A survey on intron and exon lengths.
- At Least One Intron Is Required for the Nonsense-Mediated Decay of Triosephosphate Isomerase mRNA: a Possible Link between Nuclear Splicing and Cytoplasmic Translation
- The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs.
- A specific subset of SR proteins shuttles continuously between the nucleus and the cytoplasm.
- Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells.
- Nonsense codon mutations in the terminal exon of the beta-globin gene are not associated with a reduction in beta-mRNA accumulation: a mechanism for the phenotype of dominant beta-thalassemia.
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- Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
- Pre-mRNA processing: insights from nonsense.
- Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
- Laminin-5 mutational analysis in an Italian cohort of patients with junctional epidermolysis bullosa.
- Novel RP1 mutations and a recurrent BBS1 variant explain the co-existence of two distinct retinal phenotypes in the same pedigree
- Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis
- The exon junction complex as a node of post-transcriptional networks
- A proteogenomic approach for protein-level evidence of genomic variants in cancer cells
- Making gene-modified mice.
- IL-1 Receptor Antagonist-Deficient Mice
- Vitamin A and intramuscular fat deposition: a nutrigenetic investigation in beef cattle
- Comparative analysis of eukaryotic gene sequence features
- Non-coding ribonucleic acids--a class of their own?
- Contribution à l’amélioration des connaissances sur la relation génotype-phénotype dans la mucoviscidose et caractérisation phénotypique de l’inflammation pulmonaire
- Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
- Regulation of pathways of mRNA destabilization and stabilization.
- Conditional knockout mice.
- Axonal mRNAs: functional significance in vertebrates and invertebrates
- Molecular visualization and localization of ribosomal subunits interaction in cells
- Completion of meiosis in Drosophila oocytes requires transcriptional control by grauzone, a new zinc finger protein.
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