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Published on: March 1, 2019
Murine sarcoma virus related nucleic acid sequences in a non-transforming virus derived from an interspecies
Abstract:
A number of sarcomagenic viruses recovered from hamster tumors induced originally by Moloney sarcoma virus or several of its mouse pseudotypes appear to be interspecies pseudotypes with structural proteins of hamster type-C viruses and nucleic acid sequences of both mouse and hamster specificity. A non-transforming virus (GLOH-minus) recovered from a sarcomagenic virus preparation obtained from a tumor induced by the Gross pseudotype of Moloney sarcoma virus was previously shown to retain mouse sequences. The ability to discriminate readily between Gross and Moloney viruses by molecular hybridization, especially with regard to thermal stability of inter-strain hybrid molecules, and the stability of Moloney virus sequences in a rat-mouse interspecies pseudotype, made it possible to specify that the mouse virus-specific sequences in GLOH-minus are derived from Moloney virus and not Gross. Thus, even though GLOH-minus is non-transforming in vitro or in vivo, it still retains sequences highly related to Moloney sarcoma virus. The lack of transforming ability is thus probably based on loss or change of specific sequences necessary for transformation at some point in the history of this virus.
Insights
This study identifies Moloney sarcoma virus sequences within a non-transforming virus (GLOH-minus), suggesting transformation ability loss due to sequence changes, not origin. This impacts understanding sarcoma virus evolution.
Area of Science:
- Virology
- Molecular Biology
- Oncology
Background:
- Sarcomagenic viruses can exhibit interspecies pseudotype characteristics.
- Understanding viral sequence origins is crucial for oncogenic virus research.
Purpose of the Study:
- To determine the origin of mouse-specific sequences in the non-transforming GLOH-minus virus.
- To elucidate the role of specific viral sequences in sarcomagenic transformation.
Main Methods:
- Molecular hybridization techniques were used to analyze viral nucleic acid sequences.
- Thermal stability of inter-strain hybrid molecules differentiated between Gross and Moloney viruses.
- Interspecies pseudotype analysis in rat-mouse systems.
Main Results:
- The non-transforming GLOH-minus virus retains mouse-specific sequences.
- These sequences were identified as Moloney sarcoma virus-derived, not Gross virus-derived.
- GLOH-minus, despite lacking transforming ability, shows high relatedness to Moloney sarcoma virus.
Conclusions:
- The mouse virus-specific sequences in GLOH-minus originate from Moloney sarcoma virus.
- The loss of transforming ability in GLOH-minus is likely due to alterations or loss of critical transformation-related sequences.
- This finding provides insight into the mechanisms of viral oncogenesis and evolution.
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