Literature DB >> 1658385

Transcriptional initiation and postinitiation effects of murine leukemia virus long terminal repeat R-region sequences.

L A Cupelli1, J Lenz.   

Abstract

Sequences within the R components of the long terminal repeats (LTRs) of several retroviruses are known to be involved at various steps in expression of the viral genomes. A series of experiments was performed to test whether sequences within the R regions of the murine leukemia viruses Akv and SL3-3 affect viral expression. By using plasmid clones of the viral LTRs linked to a reporter gene, deletion of the R region was found to decrease expression to variable extents in a series of mammalian cell lines, with the largest effects being detected in murine fibroblasts. R-region sequences from the human immunodeficiency virus type 1 LTR or a random sequence were unable to substitute for the murine leukemia virus sequences. Transcripts from the R-region-deleted templates were initiated at the proper site in the LTR, but their levels were decreased at least 10-fold. Nuclear run-on assays showed that the decrease caused by the R-region deletions was due, in part, to an effect on RNA polymerase loading, suggesting an effect on transcriptional initiation. The remainder of the activity was presumably due to a posttranscriptional effect. Analysis of the R-region sequences of murine leukemia viruses and related retroviruses led to the prediction of a conserved secondary structure in the transcribed RNA that might have a role in activity. We conclude that R-region sequences are of importance for the expression of a variety of retroviruses.

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Year:  1991        PMID: 1658385      PMCID: PMC250808     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  52 in total

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  10 in total

1.  R region sequences in the long terminal repeat of a murine retrovirus specifically increase expression of unspliced RNAs.

Authors:  A M Trubetskoy; S A Okenquist; J Lenz
Journal:  J Virol       Date:  1999-04       Impact factor: 5.103

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3.  The secondary structure of the R region of a murine leukemia virus is important for stimulation of long terminal repeat-driven gene expression.

Authors:  L Cupelli; S A Okenquist; A Trubetskoy; J Lenz
Journal:  J Virol       Date:  1998-10       Impact factor: 5.103

4.  Tissue- and tumor-specific targeting of murine leukemia virus-based replication-competent retroviral vectors.

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5.  The U3 region of Moloney murine leukemia virus contains position-independent cis-acting sequences involved in the nuclear export of full-length viral transcripts.

Authors:  Natalia A Volkova; Elena G Fomina; Viktoryia V Smolnikova; Natalia A Zinovieva; Igor K Fomin
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6.  The feline leukemia virus long terminal repeat contains a potent genetic determinant of T-cell lymphomagenicity.

Authors:  J Pantginis; R M Beaty; L S Levy; J Lenz
Journal:  J Virol       Date:  1997-12       Impact factor: 5.103

7.  Transcriptional regulation of porcine endogenous retroviruses released from porcine and infected human cells by heterotrimeric protein complex NF-Y and impact of immunosuppressive drugs.

Authors:  Gregor Scheef; Nicole Fischer; Egbert Flory; Isabel Schmitt; Ralf R Tönjes
Journal:  J Virol       Date:  2002-12       Impact factor: 5.103

8.  Transcriptional interaction between retroviral long terminal repeats (LTRs): mechanism of 5' LTR suppression and 3' LTR promoter activation of c-myc in avian B-cell lymphomas.

Authors:  C F Boerkoel; H J Kung
Journal:  J Virol       Date:  1992-08       Impact factor: 5.103

9.  Identification of homeodomain proteins, PBX1 and PREP1, involved in the transcription of murine leukemia virus.

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10.  Evolutionary conservation of orthoretroviral long terminal repeats (LTRs) and ab initio detection of single LTRs in genomic data.

Authors:  Farid Benachenhou; Patric Jern; Merja Oja; Göran Sperber; Vidar Blikstad; Panu Somervuo; Samuel Kaski; Jonas Blomberg
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  10 in total

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