Research Article: Murine Leukemia Viruses: Objects and Organisms

Date Published: November 15, 2011

Publisher: Hindawi Publishing Corporation

Author(s): Alan Rein.


Murine leukemia viruses (MLVs) are among the simplest retroviruses. Prototypical gammaretroviruses encode only the three polyproteins that will be used in the assembly of progeny virus particles. These are the Gag polyprotein, which is the structural protein of a retrovirus particle, the Pol protein, comprising the three retroviral enzymes—protease, which catalyzes the maturation of the particle, reverse transcriptase, which copies the viral RNA into DNA upon infection of a new host cell, and integrase, which inserts the DNA into the chromosomal DNA of the host cell, and the Env polyprotein, which induces the fusion of the viral membrane with that of the new host cell, initiating infection. In general, a productive MLV infection has no obvious effect upon host cells. Although gammaretroviral structure and replication follow the same broad outlines as those of other retroviruses, we point out a number of significant differences between different retroviral genera.

Partial Text

A virus can be viewed as a rather regular, relatively simple physical object. Alternatively, it can be seen as a living organism, evolving in response to selective pressures. Both views are correct! This paper will outline very briefly some of the characteristics of murine leukemia viruses (MLVs), keeping both views in mind. We will try to point out the distinctive features of these retroviruses, which are often taken as prototypes of the gammaretrovirus genus. (Retroviruses include Spumaretroviruses (also known as “foamy viruses”) and Orthoretroviruses; the latter are divided into six genera, that is, alpha-, beta-, gamma-, delta-, epsilon-, and lenti-retroviruses [1].)

It is clear that MLVs have provided an extraordinary wealth of information about retroviruses, both as physical objects and as living organisms. They (and other gammaretroviruses, such as gibbon ape leukemia virus) are now being developed as vectors for gene therapy. As has been indicated throughout this paper, the contrasts with other retroviruses such as HIV-1 help to illustrate the range of possibilities by which viruses solve common problems. Finally, as with all viruses, MLVs provide a window into the “black box”, an unparalleled opportunity to learn about the cells and organisms that they infect. Indeed, many cellular proteins have been shown to participate in MLV replication; while this large topic is beyond the scope of this paper, it is the focus of a fascinating review by Goff [128].




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