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Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Pathogenic potential of myeloblastosis-associated viruses
1UFR de Biochimie, Université Paris 7-D Diderot, France.
Abstract:
Myeloblastosis-associated viruses (MAV) are replication competent avian retroviruses responsible for the induction of lymphoid leukosis, osteopetrosis, and nephroblastoma. Although both the route of infection and the strain of host used has been reported to be a critical factor in determining the outcome of viral infection, genetically distinct strains of MAV that exhibit a multiple pathogenic potential have been molcularly cloned. Osteopetrosis is a proliferative disease of the bones and nephroblastoma is a kidney cancer. Both diseases occur in chickens a few weeks after MAV injection. In both cases, the nature of the target cells and mechanisms of transformation induced by MAV remain to be established. Molecular cloning and sequencing of three MAV proviral genomes inducing both osteopetrosis and nephroblastoma or only nephroblastoma have allowed the identification of viral determinants essential for osteopetrosis induction. For the last decade we have focused our attention on the MAV-induced nephroblastoma because it is a unique animal model of the human Wilms' tumor. Studies that we have conducted to understand the molecular basis of MAV tumorigenic potential have led to the identification of viral sequences required for tumor induction and to the discovery of a new cellular gene (nov) likely to play a critical role in avian and human nephroblastoma development.
Insights
Myeloblastosis-associated viruses (MAV) cause bone and kidney cancers in chickens. Researchers identified viral factors and a new gene (nov) crucial for MAV-induced nephroblastoma, a model for human Wilms' tumor.
Area of Science:
- Oncology
- Virology
- Genetics
Background:
- Myeloblastosis-associated viruses (MAV) are retroviruses causing lymphoid leukosis, osteopetrosis, and nephroblastoma in chickens.
- MAV strains with multiple pathogenic potentials have been molecularly cloned, but target cells and transformation mechanisms remain unclear.
- MAV-induced nephroblastoma serves as a unique animal model for human Wilms' tumor.
Purpose of the Study:
- To investigate the molecular basis of MAV-induced tumorigenesis.
- To identify viral determinants responsible for osteopetrosis induction.
- To understand the role of novel cellular genes in nephroblastoma development.
Main Methods:
- Molecular cloning and sequencing of three MAV proviral genomes.
- Analysis of viral sequences associated with osteopetrosis and nephroblastoma.
- Identification and characterization of a novel cellular gene (nov).
Main Results:
- Identified specific viral determinants essential for osteopetrosis induction.
- Discovered a new cellular gene, nov, implicated in MAV-induced nephroblastoma.
- Established MAV-induced nephroblastoma as a relevant model for studying human kidney cancer.
Conclusions:
- MAV possesses specific genetic elements that dictate its oncogenic potential.
- The novel gene 'nov' is a key player in avian and potentially human nephroblastoma.
- Further research into MAV and nov can advance understanding of kidney cancer and Wilms' tumor.
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