Literature DB >> 6836917

Variants of type-C retroviruses from DBA/2 mice: protein-structural and biological properties.

B A Nexø, K Ulrich.   

Abstract

Ecotropic murine leukemia viruses isolated from normal and carcinogen-treated DBA/2 mice can be classified into three main groups that differ in structure and biology. Two groups, called Ea and Eb, consist of N-tropic viruses related to the standard endogenous ecotropic virus of AKR mice. Ea viruses replicate with reduced efficiency in cell lines derived from C3H mice, while Eb viruses essentially replicate normally in these cells. As elsewhere reported, Ea viruses appear apathogenic in C3H mice, while Eb viruses cause a moderate incidence of late leukemias. The biological differences are associated with modulations of the fine structure of the gag gene-encoded proteins. A third group of viruses, called Ec, is clearly more diverged. They differ extensively from Ea and Eb viruses in the products of the gag and env gene, and are related to Rauscher leukemia virus. Ec viruses are NB-ecotropic; they replicate efficiently in all mouse cells tested, and induce leukemias in C3H mice with shorter latency periods than Eb viruses. Since published nucleic acid hybridization data indicate that DBA/2 mice only carry one ecotropic provirus, we assume that the DBA/2 viruses represent a developmental series of variants evolving during the life of the animals.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6836917     DOI: 10.1016/0042-6822(83)90216-7

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


  10 in total

1.  Poorly expressed endogenous ecotropic provirus of DBA/2 mice encodes a mutant Pr65gag protein that is not myristylated.

Authors:  N G Copeland; N A Jenkins; B Nexø; A M Schultz; A Rein; T Mikkelsen; P Jørgensen
Journal:  J Virol       Date:  1988-02       Impact factor: 5.103

2.  A new theory on autoimmunity with reference to multiple sclerosis.

Authors:  Bjørn A Nexø
Journal:  Immunol Res       Date:  2018-06       Impact factor: 2.829

3.  A domain of murine retrovirus surface protein gp70 mediates cell fusion, as shown in a novel SC-1 cell fusion system.

Authors:  K B Andersen
Journal:  J Virol       Date:  1994-05       Impact factor: 5.103

4.  Treatment of mice with 5-azacytidine efficiently activates silent retroviral genomes in different tissues.

Authors:  R Jaenisch; A Schnieke; K Harbers
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

5.  Spontaneous expression of C-type virus in DBA/2 mice is associated with an increased rate of mortality, independent of neoplastic disease.

Authors:  K Ulrich; B A Nexø
Journal:  J Virol       Date:  1985-01       Impact factor: 5.103

6.  Mechanism of chemical activation of expression of the endogenous ecotropic murine leukemia provirus Emv-3.

Authors:  J A Mercer; K H Lee; B A Nexø; N A Jenkins; N G Copeland
Journal:  J Virol       Date:  1990-05       Impact factor: 5.103

7.  Lack of ecotropic virus involvement in induction of lymphomas in DBA/2J mice by 7,12-dimethylbenz(a)anthracene.

Authors:  J A Mercer; N A Jenkins; N G Copeland
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

8.  A replication-competent, endogenous retrovirus from an aged DBA/2 mouse contains the complete env from Emv-3 and a novel gag partially related to AKT-8.

Authors:  T Bartman; D M Murasko; K J Blank
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

9.  DNAs of two molecularly cloned endogenous ecotropic proviruses are poorly infectious in DNA transfection assays.

Authors:  N G Copeland; H G Bedigian; C Y Thomas; N A Jenkins
Journal:  J Virol       Date:  1984-02       Impact factor: 5.103

Review 10.  Characterization of gP85gag as an antigen recognized by Moloney leukemia virus-specific cytolytic T cell clones that function in vivo.

Authors:  F A van der Hoorn; T Lahaye; V Müller; M A Ogle; H D Engers
Journal:  J Exp Med       Date:  1985-07-01       Impact factor: 14.307

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.