Literature DB >> 8065363

Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance.

J Cheng1, P Belgrader, X Zhou, L E Maquat.   

Abstract

The translation of human triosephosphate isomerase (TPI) mRNA normally terminates at codon 249 within exon 7, the final exon. Frameshift and nonsense mutations of the type that cause translation to terminate prematurely at or upstream of codon 189 within exon 6 reduce the level of nuclear TPI mRNA to 20 to 30% of normal by a mechanism that is not a function of the distance of the nonsense codon from either the translation initiation or termination codon. In contrast, frameshift and nonsense mutations of another type that cause translation to terminate prematurely at or downstream of codon 208, also within exon 6, have no effect on the level of nuclear TPI mRNA. In this work, quantitations of RNA that derived from TPI alleles in which nonsense codons had been generated between codons 189 and 208 revealed that the boundary between the two types of nonsense codons resides between codons 192 and 195. The analysis of TPI gene insertions and deletions indicated that the positional feature differentiating the two types of nonsense codons is the distance of the nonsense codon upstream of intron 6. For example, the movement of intron 6 to a position downstream of its normal location resulted in a concomitant downstream movement of the boundary between the two types of nonsense codons. The analysis of intron 6 mutations indicated that the intron 6 effect is stipulated by the 88 nucleotides residing between the 5' and 3' splice sites. Since the deletion of intron 6 resulted in only partial abrogation of the nonsense codon-mediated reduction in the level of TPI mRNA, other sequences within TPI pre-mRNA must function in the effect. One of these sequences may be intron 2, since the deletion of intron 2 also resulted in partial abrogation of the effect. In experiments that switched introns 2 and 6, the replacement of intron 6 with intron 2 was of no consequence to the effect of a nonsense codon within either exon 1 or exon 6. In contrast, the replacement of intron 2 with intron 6 was inconsequential to the effect of a nonsense codon in exon 6 but resulted in partial abrogation of a nonsense codon in exon 1.

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Year:  1994        PMID: 8065363      PMCID: PMC359158          DOI: 10.1128/mcb.14.9.6317-6325.1994

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  36 in total

1.  Sequence specificity of the human mRNA N6-adenosine methylase in vitro.

Authors:  J E Harper; S M Miceli; R J Roberts; J L Manley
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

Review 2.  Antisense RNA.

Authors:  Y Eguchi; T Itoh; J Tomizawa
Journal:  Annu Rev Biochem       Date:  1991       Impact factor: 23.643

3.  A single base deletion in the Tfm androgen receptor gene creates a short-lived messenger RNA that directs internal translation initiation.

Authors:  M L Gaspar; T Meo; P Bourgarel; J L Guenet; M Tosi
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

4.  Nonsense codons within the Rous sarcoma virus gag gene decrease the stability of unspliced viral RNA.

Authors:  G F Barker; K Beemon
Journal:  Mol Cell Biol       Date:  1991-05       Impact factor: 4.272

5.  Sequence specificity of mRNA N6-adenosine methyltransferase.

Authors:  T Csepany; A Lin; C J Baldick; K Beemon
Journal:  J Biol Chem       Date:  1990-11-25       Impact factor: 5.157

6.  Translation is required for regulation of histone mRNA degradation.

Authors:  R A Graves; N B Pandey; N Chodchoy; W F Marzluff
Journal:  Cell       Date:  1987-02-27       Impact factor: 41.582

7.  Translation to near the distal end of the penultimate exon is required for normal levels of spliced triosephosphate isomerase mRNA.

Authors:  J Cheng; M Fogel-Petrovic; L E Maquat
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

8.  Nonsense mutations in the dihydrofolate reductase gene affect RNA processing.

Authors:  G Urlaub; P J Mitchell; C J Ciudad; L A Chasin
Journal:  Mol Cell Biol       Date:  1989-07       Impact factor: 4.272

9.  Nonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.

Authors:  P Belgrader; L E Maquat
Journal:  Mol Cell Biol       Date:  1994-09       Impact factor: 4.272

10.  The product of the yeast UPF1 gene is required for rapid turnover of mRNAs containing a premature translational termination codon.

Authors:  P Leeds; S W Peltz; A Jacobson; M R Culbertson
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

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  60 in total

1.  Splicing and 3' end formation in the definition of nonsense-mediated decay-competent human beta-globin mRNPs.

Authors:  G Neu-Yilik; N H Gehring; R Thermann; U Frede; M W Hentze; A E Kulozik
Journal:  EMBO J       Date:  2001-02-01       Impact factor: 11.598

2.  The Y14 protein communicates to the cytoplasm the position of exon-exon junctions.

Authors:  V N Kim; J Yong; N Kataoka; L Abel; M D Diem; G Dreyfuss
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

Review 3.  mRNA surveillance in eukaryotes: kinetic proofreading of proper translation termination as assessed by mRNP domain organization?

Authors:  P Hilleren; R Parker
Journal:  RNA       Date:  1999-06       Impact factor: 4.942

4.  Pre-mRNA splicing alters mRNP composition: evidence for stable association of proteins at exon-exon junctions.

Authors:  H Le Hir; M J Moore; L E Maquat
Journal:  Genes Dev       Date:  2000-05-01       Impact factor: 11.361

Review 5.  Killing the messenger: new insights into nonsense-mediated mRNA decay.

Authors:  Peter H Byers
Journal:  J Clin Invest       Date:  2002-01       Impact factor: 14.808

6.  The exon-exon junction complex provides a binding platform for factors involved in mRNA export and nonsense-mediated mRNA decay.

Authors:  H Le Hir; D Gatfield; E Izaurralde; M J Moore
Journal:  EMBO J       Date:  2001-09-03       Impact factor: 11.598

7.  Boundary-independent polar nonsense-mediated decay.

Authors:  Jun Wang; Jayanthi P Gudikote; O Renee Olivas; Miles F Wilkinson
Journal:  EMBO Rep       Date:  2002-02-15       Impact factor: 8.807

8.  Efficient downregulation of immunoglobulin mu mRNA with premature translation-termination codons requires the 5'-half of the VDJ exon.

Authors:  Marc Bühler; Alexandra Paillusson; Oliver Mühlemann
Journal:  Nucleic Acids Res       Date:  2004-06-21       Impact factor: 16.971

9.  Mammalian nonsense codons can be cis effectors of nuclear mRNA half-life.

Authors:  P Belgrader; J Cheng; X Zhou; L S Stephenson; L E Maquat
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

10.  At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation.

Authors:  J Zhang; X Sun; Y Qian; J P LaDuca; L E Maquat
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

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