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The Gag cleavage product, p12, is a functional constituent of the murine leukemia virus pre-integration complex.
- Source :
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PLoS pathogens [PLoS Pathog] 2010 Nov 11; Vol. 6 (11), pp. e1001183. Date of Electronic Publication: 2010 Nov 11. - Publication Year :
- 2010
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Abstract
- The p12 protein is a cleavage product of the Gag precursor of the murine leukemia virus (MLV). Specific mutations in p12 have been described that affect early stages of infection, rendering the virus replication-defective. Such mutants showed normal generation of genomic DNA but no formation of circular forms, which are markers of nuclear entry by the viral DNA. This suggested that p12 may function in early stages of infection but the precise mechanism of p12 action is not known. To address the function and follow the intracellular localization of the wt p12 protein, we generated tagged p12 proteins in the context of a replication-competent virus, which allowed for the detection of p12 at early stages of infection by immunofluorescence. p12 was found to be distributed to discrete puncta, indicative of macromolecular complexes. These complexes were localized to the cytoplasm early after infection, and thereafter accumulated adjacent to mitotic chromosomes. This chromosomal accumulation was impaired for p12 proteins with a mutation that rendered the virus integration-defective. Immunofluorescence demonstrated that intracellular p12 complexes co-localized with capsid, a known constituent of the MLV pre-integration complex (PIC), and immunofluorescence combined with fluorescent in situ hybridization (FISH) revealed co-localization of the p12 proteins with the incoming reverse transcribed viral DNA. Interactions of p12 with the capsid and with the viral DNA were also demonstrated by co-immunoprecipitation. These results imply that p12 proteins are components of the MLV PIC. Furthermore, a large excess of wt PICs did not rescue the defect in integration of PICs derived from mutant p12 particles, demonstrating that p12 exerts its function as part of this complex. Altogether, these results imply that p12 proteins are constituent of the MLV PIC and function in directing the PIC from the cytoplasm towards integration.
- Subjects :
- Animals
Blotting, Western
Bone Neoplasms metabolism
Bone Neoplasms pathology
Bone Neoplasms virology
Cells, Cultured
Chromosomes, Mammalian genetics
DNA, Viral genetics
DNA, Viral metabolism
Fibroblasts metabolism
Fibroblasts virology
Fluorescent Antibody Technique
Gene Products, gag genetics
Humans
Immunoprecipitation
In Situ Hybridization, Fluorescence
Kidney cytology
Kidney metabolism
Kidney virology
Leukemia, Experimental pathology
Leukemia, Experimental virology
Mice
Mitosis physiology
Mutation genetics
NIH 3T3 Cells
Osteosarcoma metabolism
Osteosarcoma pathology
Osteosarcoma virology
Phylogeny
RNA, Messenger genetics
Retroviridae Infections pathology
Retroviridae Infections virology
Reverse Transcriptase Polymerase Chain Reaction
Tumor Virus Infections pathology
Tumor Virus Infections virology
Virus Replication
Gene Products, gag chemistry
Gene Products, gag metabolism
Leukemia Virus, Murine physiology
Leukemia, Experimental metabolism
Retroviridae Infections metabolism
Tumor Virus Infections metabolism
Virus Assembly
Subjects
Details
- Language :
- English
- ISSN :
- 1553-7374
- Volume :
- 6
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- PLoS pathogens
- Publication Type :
- Academic Journal
- Accession number :
- 21085616
- Full Text :
- https://doi.org/10.1371/journal.ppat.1001183