Literature DB >> 6314644

Site-specific mutagenesis of avian erythroblastosis virus: v-erb-A is not required for transformation of fibroblasts.

L Sealy, G Moscovici, C Moscovici, J M Bishop.   

Abstract

Avian erythroblastosis virus (AEV) is an acutely transforming retrovirus whose putative oncogenes (v-erb-A and v-erb-B) encode the proteins P74gag-erb-A and P61-68erb-B. The existence of these two gene products has prompted the question of whether one or both proteins are required in the transformation of erythroblasts and fibroblasts by AEV. In the accompanying manuscript, we describe the use of site-specific mutagenesis to generate mutants of AEV unable to synthesize P61-68erb-B. Here we present our analysis of the oncogenic potential of an AEV mutant unable to synthesize P74gag-erb-A due to a large deletion encompassing both gag and v-erb-A sequences. The erb-A-mutant retrovirus propagated quite poorly on fibroblasts in culture; however, fibroblasts harboring the erb-A mutant genome were transformed in the absence of P74gag-erb-A expression. The mutant virus failed to induce erythroleukemias in chickens, but the validity of this finding is compromised by the poor replicative capacity of the mutant. The results presented in this and the preceding manuscript indicate that P61-68erb-B is both necessary and sufficient for neoplastic transformation of fibroblasts by AEV; by contrast, a role for p74gag-erb-A in leukemogenesis by AEV has not yet been rigorously excluded.

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Year:  1983        PMID: 6314644     DOI: 10.1016/0042-6822(83)90126-5

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


  24 in total

1.  The amino-terminal 14 amino acids of v-src can functionally replace the extracellular and transmembrane domains of v-erbB.

Authors:  M McMahon; R C Schatzman; J M Bishop
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

2.  Sequence-specific DNA binding by the v-erbA oncogene protein of avian erythroblastosis virus.

Authors:  B G Bonde; M L Privalsky
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

3.  c-erbA encodes multiple proteins in chicken erythroid cells.

Authors:  J Bigler; R N Eisenman
Journal:  Mol Cell Biol       Date:  1988-10       Impact factor: 4.272

4.  Genetic dissection of functional domains within the avian erythroblastosis virus v-erbA oncogene.

Authors:  M L Privalsky; P Boucher; A Koning; C Judelson
Journal:  Mol Cell Biol       Date:  1988-10       Impact factor: 4.272

5.  The avian erythroblastosis virus erbA oncogene encodes a DNA-binding protein exhibiting distinct nuclear and cytoplasmic subcellular localizations.

Authors:  P Boucher; A Koning; M L Privalsky
Journal:  J Virol       Date:  1988-02       Impact factor: 5.103

6.  Bacterial beta-galactosidase as a marker of Rous sarcoma virus gene expression and replication.

Authors:  P A Norton; J M Coffin
Journal:  Mol Cell Biol       Date:  1985-02       Impact factor: 4.272

7.  Dispersed chromosomal localization of the proto-oncogenes transduced into the genome of Mill Hill 2 or E26 leukemia virus.

Authors:  G Symonds; N Quintrell; E Stubblefield; J M Bishop
Journal:  J Virol       Date:  1986-07       Impact factor: 5.103

8.  Orientation of the v-erb-B gene product in the plasma membrane.

Authors:  R C Schatzman; G I Evan; M L Privalsky; J M Bishop
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

9.  Nucleotide sequence of avian carcinoma virus MH2: two potential onc genes, one related to avian virus MC29 and the other related to murine sarcoma virus 3611.

Authors:  N C Kan; C S Flordellis; G E Mark; P H Duesberg; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

10.  Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man.

Authors:  B U Zabel; R E Fournier; P A Lalley; S L Naylor; A Y Sakaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

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