Literature DB >> 6203214

FBR murine osteosarcoma virus. I. Molecular analysis and characterization of a 75,000-Da gag-fos fusion product.

T Curran, I M Verma.   

Abstract

The FBR murine osteosarcoma virus complex induces bone tumors with a similar latency and pathology to those induced by the FBJ virus complex. FBR murine sarcoma virus ( FBR -MSV) has been isolated from its helper virus(es) by the establishment of transformed nonproducer cells. These cells were found to express a 75,000-Da protein (P75) which was antigenically related to the p55 oncogene product of the FBJ murine osteosarcoma virus ( FBJ -MSV). P75 also contained antigenic determinants of murine leukemia virus (MLV) gag gene p15, p12, and p30 proteins, and is therefore a gag- fos fusion protein ( P75gag - fos ). P75gag - fos is a phosphoprotein and is found primarily in the nucleus. Only a single species of RNA, of 3.3 kb, was identified in FBR -MSV-transformed nonproducer cells using both fos and MLV probes, which suggested that P75gag - fos was expressed from genome-sized RNA. Chromosomal DNA from one nonproducer cell line was found to contain a single EcoRI restriction fragment of 12 kb pairs (kbp) which encompassed the FBR -MSV provirus. This DNA fragment was molecularly cloned into bacteriophage Charon 30 (lambda FBR -1), and a 7.5-kbp HindIII restriction fragment containing the entire provirus was subsequently subcloned into pBR322 ( pFBR -1). DNA from pFBR -1 was capable of inducing morphological transformation of mouse and rat fibroblasts in tissue culture. In addition, transfected cells expressed the FBR -MSV P75gag - fos protein.

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Year:  1984        PMID: 6203214     DOI: 10.1016/0042-6822(84)90132-6

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  23 in total

1.  Expression and purification of the leucine zipper and DNA-binding domains of Fos and Jun: both Fos and Jun contact DNA directly.

Authors:  C Abate; D Luk; R Gentz; F J Rauscher; T Curran
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

2.  Revertants of v-fos-transformed rat fibroblasts: suppression of transformation is dominant.

Authors:  R Wisdom; I M Verma
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

3.  Transcriptional activation and repression by Fos are independent functions: the C terminus represses immediate-early gene expression via CArG elements.

Authors:  D Gius; X M Cao; F J Rauscher; D R Cohen; T Curran; V P Sukhatme
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

4.  Isolation and characterization of fra-2, an additional member of the fos gene family.

Authors:  H Nishina; H Sato; T Suzuki; M Sato; H Iba
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

5.  Molecular evolutionary rates of oncogenes.

Authors:  T Gojobori; S Yokoyama
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

6.  Decreased susceptibility to calpains of v-FosFBR but not of v-FosFBJ or v-JunASV17 retroviral proteins compared with their cellular counterparts.

Authors:  A M Steff; S Carillo; M Pariat; M Piechaczyk
Journal:  Biochem J       Date:  1997-05-01       Impact factor: 3.857

7.  Myristylation alters DNA-binding activity and transactivation of FBR (gag-fos) protein.

Authors:  N Kamata; R M Jotte; J T Holt
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

8.  Cell transformation by c-fos requires an extended period of expression and is independent of the cell cycle.

Authors:  G G Miao; T Curran
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

9.  c-fos and its Consequences in Pain.

Authors:  Asma Hayati Ahmad; Zalina Ismail
Journal:  Malays J Med Sci       Date:  2002-01

10.  fra-1: a serum-inducible, cellular immediate-early gene that encodes a fos-related antigen.

Authors:  D R Cohen; T Curran
Journal:  Mol Cell Biol       Date:  1988-05       Impact factor: 4.272

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