Trim5α protein restricts both HIV-1 and murine leukemia virus

Replication of HIV-1 and N-tropic murine leukemia virus (N-MLV) is restricted in a number of different primate cells. In some cell lines, cross-saturation experiments suggest that the two viruses are interacting with the same restriction factor. Recently, Trim5α protein from rhesus monkey was found to restrict HIV-1. We have confirmed this result and have shown that Trim5α from two African green monkey cell lines, Vero and CV-1, also restricts HIV-1. In addition, we show that human, rhesus, and African green monkey Trim5α can restrict N-MLV. By using a panel of MLV capsid mutants, subtle differences in the anti-MLV activity were identified among the different primate Trim5α cDNAs. Trim1 isolated from humans and green monkeys was also found to restrict N-MLV. We hypothesize that the Trim family of proteins plays a widespread role in innate immunity to viral infection.

[1]  A. Burt,et al.  Long-term reinfection of the human genome by endogenous retroviruses. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Sean J. Johnson,et al.  Structures of Mismatch Replication Errors Observed in a DNA Polymerase , 2004, Cell.

[3]  C. M. Owens,et al.  The cytoplasmic body component TRIM5α restricts HIV-1 infection in Old World monkeys , 2004, Nature.

[4]  P. Bieniasz,et al.  Cyclophilin A modulates the sensitivity of HIV-1 to host restriction factors , 2003, Nature Medicine.

[5]  P. Bieniasz Restriction factors: a defense against retroviral infection. , 2003, Trends in microbiology.

[6]  P. Bieniasz,et al.  Restriction of multiple divergent retroviruses by Lv1 and Ref1 , 2003, The EMBO journal.

[7]  G. Lucero,et al.  A dominant block to HIV-1 replication at reverse transcription in simian cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[8]  J. Stoye An intracellular block to primate lentivirus replication , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[9]  P. Bieniasz,et al.  Cellular inhibitors with Fv1-like activity restrict human and simian immunodeficiency virus tropism , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Y. Takeuchi,et al.  Restriction of lentivirus in monkeys , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Roger E Bumgarner,et al.  Cellular transcriptional profiling in influenza A virus-infected lung epithelial cells: The role of the nonstructural NS1 protein in the evasion of the host innate defense and its potential contribution to pandemic influenza , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Kathryn L. Parsley,et al.  In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium , 2001, Gene Therapy.

[13]  D. Trono,et al.  Cytoplasmic recruitment of INI1 and PML on incoming HIV preintegration complexes: interference with early steps of viral replication. , 2001, Molecular cell.

[14]  G. Towers,et al.  Identification of the Regions of Fv1 Necessary for Murine Leukemia Virus Restriction , 2001, Journal of Virology.

[15]  Alessandro Guffanti,et al.  The tripartite motif family identifies cell compartments , 2001, The EMBO journal.

[16]  Y. Takeuchi,et al.  A conserved mechanism of retrovirus restriction in mammals. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[17]  G. Towers,et al.  Use of a Transient Assay for Studying the Genetic Determinants of Fv1 Restriction , 2000, Journal of Virology.

[18]  J. Sodroski,et al.  Species-Specific, Postentry Barriers to Primate Immunodeficiency Virus Infection , 1999, Journal of Virology.

[19]  J. Coffin,et al.  Constructing primate phylogenies from ancient retrovirus sequences. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[20]  A. Ballabio,et al.  MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development. , 1999, Human molecular genetics.

[21]  M. Whitlow,et al.  Protein fold analysis of the B30.2‐like domain , 1999, Proteins.

[22]  P. Pontarotti,et al.  B30.2-like domain proteins: update and new insights into a rapidly expanding family of proteins. , 1998, Molecular biology and evolution.

[23]  F. Bonhomme,et al.  Molecular phylogeny of Fv1 , 1998, Mammalian Genome.

[24]  H. de Thé,et al.  Resistance to Virus Infection Conferred by the Interferon-Induced Promyelocytic Leukemia Protein , 1998, Journal of Virology.

[25]  B. Chesebro,et al.  Immunity to retroviral infection: the Friend virus model. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[26]  C. Kozak,et al.  Single amino acid changes in the murine leukemia virus capsid protein gene define the target of Fv1 resistance. , 1996, Virology.

[27]  Jonathan P. Stoye,et al.  Positional cloning of the mouse retrovirus restriction gene Fvl , 1996, Nature.

[28]  F. Gage,et al.  In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral Vector , 1996, Science.

[29]  A. Kingsman,et al.  A transient three-plasmid expression system for the production of high titer retroviral vectors. , 1995, Nucleic acids research.

[30]  D. Mager,et al.  Recent evolutionary expansion of a subfamily of RTVL-H human endogenous retrovirus-like elements. , 1993, Virology.

[31]  F. Lilly Fv-2: identification and location of a second gene governing the spleen focus response to Friend leukemia virus in mice. , 1970, Journal of the National Cancer Institute.

[32]  R. Huebner,et al.  Host-Range Restrictions of Murine Leukemia Viruses in Mouse Embryo Cell Cultures , 1970, Journal of virology.

[33]  S. O’Brien,et al.  The Lake Casitas wild mouse: evolving genetic resistance to retroviral disease. , 1991, Trends in genetics : TIG.