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Splicing is required for rapid and efficient mRNA export in metazoans.
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Roles of U4 and U6 snRNAs in the assembly of splicing complexes.
EMBO J. 1992 Jan;11(1):335-43
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REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.
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Pre-mRNA splicing alters mRNP composition: evidence for stable association of proteins at exon-exon junctions.
Genes Dev. 2000 May 1;14(9):1098-108
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The acute myeloid leukemia-associated protein, DEK, forms a splicing-dependent interaction with exon-product complexes.
J Cell Biol. 2000 Jul 24;150(2):309-20
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The protein Aly links pre-messenger-RNA splicing to nuclear export in metazoans.
Nature. 2000 Sep 21;407(6802):401-5
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Pre-mRNA splicing imprints mRNA in the nucleus with a novel RNA-binding protein that persists in the cytoplasm.
Mol Cell. 2000 Sep;6(3):673-82
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Identification and characterization of human orthologues to Saccharomyces cerevisiae Upf2 protein and Upf3 protein (Caenorhabditis elegans SMG-4).
Mol Cell Biol. 2001 Jan;21(1):209-23
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The spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctions.
EMBO J. 2000 Dec 15;19(24):6860-9
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Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon.
Cell. 2000 Dec 22;103(7):1121-31
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Splicing and 3' end formation in the definition of nonsense-mediated decay-competent human beta-globin mRNPs.
EMBO J. 2001 Feb 1;20(3):532-40
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REF proteins mediate the export of spliced and unspliced mRNAs from the nucleus.
Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):1030-5
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Initial sequencing and analysis of the human genome.
Nature. 2001 Feb 15;409(6822):860-921
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The Y14 protein communicates to the cytoplasm the position of exon-exon junctions.
EMBO J. 2001 Apr 17;20(8):2062-8
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Mammalian heat shock p70 and histone H4 transcripts, which derive from naturally intronless genes, are immune to nonsense-mediated decay.
RNA. 2001 Mar;7(3):445-56
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Nucleocytoplasmic transport enters the atomic age.
Curr Opin Cell Biol. 2001 Jun;13(3):310-9
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Overexpression of TAP/p15 heterodimers bypasses nuclear retention and stimulates nuclear mRNA export.
J Biol Chem. 2001 Jun 8;276(23):20536-43
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Communication of the position of exon-exon junctions to the mRNA surveillance machinery by the protein RNPS1.
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Molecular consequences of truncations of the first exon for in vitro splicing of yeast actin pre-mRNA.
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The role of the mammalian branchpoint sequence in pre-mRNA splicing.
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Nuclear export of different classes of RNA is mediated by specific factors.
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Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance.
Mol Cell Biol. 1994 Sep;14(9):6317-25
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A splicing-dependent regulatory mechanism that detects translation signals.
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Cloning and characterization of HUPF1, a human homolog of the Saccharomyces cerevisiae nonsense mRNA-reducing UPF1 protein.
Nucleic Acids Res. 1997 Feb 15;25(4):814-21
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Upf1p, Nmd2p, and Upf3p are interacting components of the yeast nonsense-mediated mRNA decay pathway.
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The simian retrovirus-1 constitutive transport element, unlike the HIV-1 RRE, uses factors required for cellular mRNA export.
Curr Biol. 1997 Sep 1;7(9):619-28
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The constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV) accesses a cellular mRNA export pathway.
EMBO J. 1997 Dec 15;16(24):7500-10
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Nonsense surveillance in lymphocytes?
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Nuclear history of a pre-mRNA determines the translational activity of cytoplasmic mRNA.
EMBO J. 1998 Apr 1;17(7):2107-21
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A coactivator of pre-mRNA splicing.
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The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs.
Genes Dev. 1998 Jun 1;12(11):1665-77
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Binary specification of nonsense codons by splicing and cytoplasmic translation.
EMBO J. 1998 Jun 15;17(12):3484-94
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A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance.
Trends Biochem Sci. 1998 Jun;23(6):198-9
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TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus.
Mol Cell. 1998 Apr;1(5):649-59
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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.
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Nucleocytoplasmic transport: the soluble phase.
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Cell. 1999 Feb 5;96(3):307-10
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RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer.
Trends Genet. 1999 Feb;15(2):74-80
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TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus.
EMBO J. 1999 Apr 1;18(7):1953-65
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The Mex67p-mediated nuclear mRNA export pathway is conserved from yeast to human.
EMBO J. 1999 May 4;18(9):2593-609
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Trans-complementation of the second step of pre-mRNA splicing by exogenous 5' exons.
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Purification and characterization of human RNPS1: a general activator of pre-mRNA splicing.
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The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates.
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