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Transgenic Fv-4 mice resistant to Friend virus.

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TLDR
The phenotype of recovery from viremia in Fv4-11 mice was unexpected and suggests that low levels of expression of the Fv-4 gene enhance the effectiveness of the immune response.
Abstract
Fv-4 is a mouse gene that confers resistance to infection with ecotropic retroviruses. A candidate Fv-4 gene was cloned previously and found to resemble the 3' half of a murine leukemia virus (MuLV). To study the effect of this gene in vivo, we generated two transgenic mouse strains carrying the Fv-4 env gene under control of its presumed natural promoter, a cellular sequence unrelated to retroviruses. Transgenic progeny expressed a 3-kb Fv-4 env RNA in all of the organs and tissues examined, as well as an Fv-4 envelope antigen on the surface of thymocytes and spleen cells, similar to mice carrying the natural Fv-4 gene. One of the two transgenic strains (designated Fv4-2) expressed three to nine times as much transgene RNA and protein as the other strain (Fv4-11). When challenged with a Friend virus complex containing up to 10(4) XC PFU of Friend MuLV, Fv4-2 mice were completely resistant to development of splenomegaly and had no detectable ecotropic virus in the spleen or blood, confirming that the cloned Fv-4 gene is responsible for resistance to ecotropic MuLV in vivo. In contrast, Fv4-11 mice were only partially resistant, developing viremia and splenomegaly at the highest inoculum dose but recovering from viremia several weeks after inoculation with 10-fold less virus. The phenotype of recovery from viremia in Fv4-11 mice was unexpected and suggests that low levels of expression of the Fv-4 gene enhance the effectiveness of the immune response.

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Journal ArticleDOI

Syncytin is a captive retroviral envelope protein involved in human placental morphogenesis.

TL;DR: It is shown that expression of recombinant syncytin in a wide variety of cell types induces the formation of giant syncytia, and that fusion of a human trophoblastic cell line expressing endogenousSyncytin can be inhibited by an anti-syncytin antiserum, and thus may be important in human placental morphogenesis.
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Retrovirus Restriction Factors

TL;DR: A number of cellular genes have recently been identified that actively inhibit retrovirus replication and so protect cells from infection and it may someday be possible to enhance or activate these systems to induce antiviral states.
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naked cuticle encodes an inducible antagonist of Wnt signalling.

TL;DR: Nkd, a Drosophila segment-polarity gene, encodes an inducible antagonist for the Wnt signal Wingless, and may link ion fluxes to the regulation of the potency, duration or distribution of Wnt signals.
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Retroviral superinfection resistance.

TL;DR: This review describes the present understanding of the underlying mechanisms of SIR established by three characteristic retroviruses: Murine Leukaemia Virus (MuLV), Foamy Virus (FV), and Human Immunodeficiency Virus (HIV).
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Genetic control of host resistance to infection

TL;DR: This work cloned several host-resistance loci that regulate natural and acquired immunity in response to infection from genetically distinct inbred strains of mice that differ in their susceptibility to specific pathogens.
References
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Book

Manipulating the mouse embryo: A laboratory manual

TL;DR: Here are recorded the tech- niques for preparing, inserting and analysing DNA sequences, for retroviral infection of mice, for production and use of EC and EK cells as vehicles for engineered sequences and for nuclear transplantation - all against a background of the basic procedures required for pro- ducing and handling the em- bryos.
Journal ArticleDOI

Delay of disease development in transgenic plants that express the tobacco mosaic virus coat protein gene.

TL;DR: The results of these experiments indicate that plants can be genetically transformed for resistance to virus disease development.
Journal ArticleDOI

Cell-free transmission in adult Swiss mice of a disease having the character of a leukemia.

TL;DR: A disease with the characteristics of a leukemia has been found to be serially transmissible in adult Swiss mice by means of cell-free filtrates and intraperitoneal, subcutaneous, intracerebral, and intramuscular injections are all effective.
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