Literature DB >> 7708717

Negative-acting factor and superantigen are separable activities of the mouse mammary tumor virus long terminal repeat.

S Wintersperger1, B Salmons, T Miethke, V Erfle, H Wagner, W H Günzburg.   

Abstract

The open reading frame contained within the long terminal repeat (LTR) of mouse mammary tumor virus encodes Naf, a negative regulator of transcription, as well as a superantigen activity, Sag, which causes the deletion of specific classes of T cells. In the present study, the effect of Naf expression on different promoters and the coding requirements for Naf and Sag have been investigated. Sag activity was found to require only sequences in the LTR, whereas sequences located within the gag gene were additionally required for functional Naf activity. Surprisingly, both the classic promoter and a recently described promoter located in the LTR can give rise to both functional Naf and Sag. Further analysis of Naf revealed that the downregulatory effect was mediated by sequences located in the LTR and that heterologous promoters were also affected by Naf.

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Year:  1995        PMID: 7708717      PMCID: PMC42295          DOI: 10.1073/pnas.92.7.2745

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  32 in total

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Journal:  Immunity       Date:  1994-04       Impact factor: 31.745

Review 4.  Subversion of host immune responses by viral superantigens.

Authors:  H Acha-Orbea; H R MacDonald
Journal:  Trends Microbiol       Date:  1993-04       Impact factor: 17.079

5.  Long terminal repeats of endogenous mouse mammary tumour virus contain a long open reading frame which extends into adjacent sequences.

Authors:  N Kennedy; G Knedlitschek; B Groner; N E Hynes; P Herrlich; R Michalides; A J van Ooyen
Journal:  Nature       Date:  1982-02-18       Impact factor: 49.962

6.  Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter.

Authors:  P J Southern; P Berg
Journal:  J Mol Appl Genet       Date:  1982

7.  Transcription of mouse mammary tumor virus: identification of a candidate mRNA for the long terminal repeat gene product.

Authors:  D A Wheeler; J S Butel; D Medina; R D Cardiff; G L Hager
Journal:  J Virol       Date:  1983-04       Impact factor: 5.103

8.  Structural analysis of a 1.7-kilobase mouse mammary tumor virus-specific RNA.

Authors:  A J van Ooyen; R J Michalides; R Nusse
Journal:  J Virol       Date:  1983-05       Impact factor: 5.103

9.  Production of mouse mammary tumor virus upon transfection of a recombinant proviral DNA into cultured cells.

Authors:  B Salmons; B Groner; C M Calberg-Bacq; H Ponta
Journal:  Virology       Date:  1985-07-15       Impact factor: 3.616

10.  Regulatory and coding potential of the mouse mammary tumor virus long terminal redundancy.

Authors:  L A Donehower; A L Huang; G L Hager
Journal:  J Virol       Date:  1981-01       Impact factor: 5.103

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  3 in total

1.  Superantigen expression is driven by both mouse mammary tumor virus long terminal repeat-associated promoters in transgenic mice.

Authors:  B Salmons; T Miethke; S Wintersperger; M Müller; G Brem; W H Günzburg
Journal:  J Virol       Date:  2000-03       Impact factor: 5.103

2.  Promoter complex in the central part of the mouse mammary tumor virus long terminal repeat.

Authors:  Francoise Rouault; Shiva Badihi Nejad Asl; Stefanie Rungaldier; Eva Fuchs; Brian Salmons; Walter H Günzburg
Journal:  J Virol       Date:  2007-08-08       Impact factor: 5.103

Review 3.  The Viral Origin of Human Breast Cancer: From the Mouse Mammary Tumor Virus (MMTV) to the Human Betaretrovirus (HBRV).

Authors:  Generoso Bevilacqua
Journal:  Viruses       Date:  2022-08-01       Impact factor: 5.818

  3 in total

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