Christine A. Kozak, Ph.D.
Viral Biology Section
Building 4, Room 329
Bethesda, MD 20892
The Viral Biology Section has a long-standing interest in the identification and characterization of genes that affect susceptibility to mouse leukemia viruses (MLVs) and to MLV-induced disease. The various inbred strains of laboratory mice and wild mouse species differ in their susceptibility to MLVs, and multiple genes are responsible for these differences. We are specifically interested in those genes that inhibit early stages of the viral replicative cycle. For these studies, we use wild mouse species as well as inbred strains of laboratory mice because the common inbred strains were derived from common progenitors and are therefore not representative of the range of genetic diversity within Mus.
Retroviruses enter cells through interaction with specific cell surface receptors. This virus-receptor interaction defines host range, contributes to pathogenesis, and can provide the basis for the evolution of restriction variants that enable natural populations to evade retrovirus infection. Entry can be blocked by mutations in the receptor gene or by host resistance factors that interfere with receptor function. Our projects have identified the following:
- Five naturally occurring functional variants of the XPR1 receptor for the pathogenic polytropic and xenotropic MLV host range groups
- Several laboratory mouse strains that are susceptible to “xenotropic” MLVs, viruses originally defined by their failure to infect mouse cells
- Critical amino acids that form the XPR1 receptor determinants and critical sites in the ecotropic MLV envelope responsible for altered host range and receptor-induced formation of multicleated syncytia
- Roles for receptor and virus-linked glycans in host range and cytopathicity
- Endogenous retrovirus insertions at two restriction loci, Rmcf and Rmcf2, which block exogenous virus infection by receptor interference
The prototype for factors that interfere with post-entry stages of virus replication is the Fv1 gene, discovered 40 years ago in studies on resistance for Friend MLV and shown to be a co-opted endogenous retrovirus. We have determined that Fv1 is present in three of the four Mus subgenera demonstrating that the gene was acquired about seven MYA. Using phylogenetic sequence analysis, we found evidence for positive selection of this gene throughout Mus evolution. We also identified novel restriction alleles and identified specific codons under positive selection. These evolutionarily important codons include two known to contribute toFv1 resistance in laboratory mice and three codons clustered in an Fv1 segment homologous to the retroviral region known to be involved in capsid multimerization. This suggests that Fv1 inhibition may result from its binding to virus capsids.
More recent studies on the mouse APOBEC3 gene have determined that this antiviral factor is polymorphic for the presence of an inserted sequence that represents the long terminal repeat of the xenotropic MLV. This sequence is found in the more antiviral allele and is associated with elevated APOBEC3 expression levels. We also showed that APOBEC3 has been under positive selection, and six of the positively selected codons specify residues that lie in two clusters that are opposite each other along the predicted active site groove; one of these clusters corresponds to a substrate recognition loop identified in human APOBEC. Most recently, we have examined the genetic basis for the inclusion of the extra exon 5 in some APOBEC3 alleles. Inclusion of this exon occurred relatively late in Mus evolution and is associated with reduced antiviral activity, suggesting that the cost of maintaining an effective but mutagenic enzyme may outweigh its antiviral function in some mouse populations.
Dr. Kozak received her Ph.D. in biology from Yale University in 1977. After a postdoctoral fellowship at NIAID under Dr. Wallace Rowe, she joined the Laboratory of Molecular Microbiology (LMM) in 1984. In 1992, Dr. Kozak became chief of the Viral Biology Section in LMM. She is an associate editor for several journals, has served on the Committee on Standardized Nomenclature for Mice, was chair of the Mouse Chromosome 5 Committee for 10 years, and has authored more than 400 research publications dealing with mouse retroviruses and mouse genetics.
Baliji S, Liu Q, Kozak CA. Common inbred strains of the laboratory mouse that are susceptible to infection by mouse xenotropic gammaretroviruses and the human-derived retrovirus XMRV. J Virol. 2010;84(24):12841-9.
Martin C, Buckler-White A, Wollenberg K, Kozak CA. The avian XPR1 gammaretrovirus receptor is under positive selection and is disabled in bird species in contact with virus-infected wild mice. J Virol. 2013;87(18):10094-104.
Sanville B, Dolan MA, Wollenberg K, Yan Y, Martin C, Yeung ML, Strebel K, Buckler-White A, Kozak CA. Adaptive evolution of Mus Apobec3 includes retroviral insertion and positive selection at two clusters of residues flanking the substrate groove. PLoS Pathog. 2010;6:e1000974.
Bamunusinghe D, Liu Q, Lu X, Oler A, Kozak CA. Endogenous gammaretrovirus acquisition in Mus musculus subspecies carrying functional variants of the XPR1 virus receptor. J Virol. 2013;87(17):9845-55.
Bamunusinghe D, Naghashfar Z, Buckler-White A, Plishka R, Baliji S, Liu Q, Kassner J, Oler AJ, Hartley J, Kozak CA. Sequence Diversity, Intersubgroup Relationships, and Origins of the Mouse Leukemia Gammaretroviruses of Laboratory and Wild Mice. J Virol. 2016;90(8):4186-98.
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This page was last updated on February 15th, 2017