Literature DB >> 2837647

Exploitation of a thermosensitive splicing event to study pre-mRNA splicing in vivo.

P E Cizdziel1, M de Mars, E C Murphy.   

Abstract

The spliced form of MuSVts110 viral RNA is approximately 20-fold more abundant at growth temperatures of 33 degrees C or lower than at 37 to 41 degrees C. This difference is due to changes in the efficiency of MuSVts110 RNA splicing rather than selective thermolability of the spliced species at 37 to 41 degrees C or general thermosensitivity of RNA splicing in MuSVts110-infected cells. Moreover, RNA transcribed from MuSVts110 DNA introduced into a variety of cell lines is spliced in a temperature-sensitive fashion, suggesting that the structure of the viral RNA controls the efficiency of the event. We exploited this novel splicing event to study the cleavage and ligation events during splicing in vivo. No spliced viral mRNA or splicing intermediates were observed in MuSVts110-infected cells (6m2 cells) at 39 degrees C. However, after a short (about 30-min) lag following a shift to 33 degrees C, viral pre-mRNA cleaved at the 5' splice site began to accumulate. Ligated exons were not detected until about 60 min following the initial detection of cleavage at the 5' splice site, suggesting that these two splicing reactions did not occur concurrently. Splicing of viral RNA in the MuSVts110 revertant 54-5A4, which lacks the sequence -AG/TGT- at the usual 3' splice site, was studied. Cleavage at the 5' splice site in the revertant viral RNA proceeded in a temperature-sensitive fashion. No novel cryptic 3' splice sites were activated; however, splicing at an alternate upstream 3' splice site used at low efficiency in normal MuSVts110 RNA was increased to a level close to that of 5'-splice-site cleavage in the revertant viral RNA. Increased splicing at this site in 54-5A4 viral RNA is probably driven by the unavailability of the usual 3' splice site for exon ligation. The thermosensitivity of this alternate splice event suggests that the sequences governing the thermodependence of MuSVts110 RNA splicing do not involve any particular 3' splice site or branch point sequence, but rather lie near the 5' end of the intron.

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Year:  1988        PMID: 2837647      PMCID: PMC363316          DOI: 10.1128/mcb.8.4.1558-1569.1988

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


  37 in total

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  8 in total

1.  Regulation of RNA splicing in gag-deficient mutants of Moloney murine sarcoma virus MuSVts110.

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2.  The Moloney murine sarcoma virus ts110 5' splice site signal contributes to the regulation of splicing efficiency and thermosensitivity.

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3.  Activation of cryptic splice sites in murine sarcoma virus-124 mutants.

Authors:  M de Mars; P E Cizdziel; E C Murphy
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Authors:  S Arrigo; K Beemon
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5.  Activation of thermosensitive RNA splicing and production of a heat-labile P85gag-mos kinase by the introduction of a specific deletion in murine sarcoma virus-124 DNA.

Authors:  M de Mars; P E Cizdziel; E C Murphy
Journal:  J Virol       Date:  1988-06       Impact factor: 5.103

6.  Moloney murine sarcoma virus MuSVts110 DNA: cloning, nucleotide sequence, and gene expression.

Authors:  L Huai; S M Chiocca; M A Gilbreth; J R Ainsworth; L A Bishop; E C Murphy
Journal:  J Virol       Date:  1992-09       Impact factor: 5.103

7.  Branchpoint and polypyrimidine tract mutations mediating the loss and partial recovery of the Moloney murine sarcoma virus MuSVts110 thermosensitive splicing phenotype.

Authors:  J W Touchman; I D'Souza; C A Heckman; R Zhou; N W Biggart; E C Murphy
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8.  Temperature regulates splicing efficiency of the cold-inducible RNA-binding protein gene Cirbp.

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  8 in total

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