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All intact subunit RNAs from Rous sarcoma virus contain poly (A)
The Journal of Biological Chemistry
|January 10, 1976
Summary
Most Schmidt-Ruppin Rous sarcoma virus RNA subunits bind deoxythymidine oligonucleotides (dT)n. Nonbinding RNAs are fragments lacking the riboadenylic acid (rA)n terminus due to nucleolytic cleavage.
Area of Science:
- Molecular Biology
- Virology
- RNA Biochemistry
Background:
- Schmidt-Ruppin Rous sarcoma virus (SRRSV) is an oncogenic retrovirus.
- Viral RNA subunits are crucial for viral replication and infectivity.
- Understanding RNA-binding properties is key to deciphering viral mechanisms.
Purpose of the Study:
- To investigate the binding capacity of SRRSV RNA subunits to deoxythymidine oligonucleotides ((dT)n).
- To characterize the nature of RNA subunits that do not bind (dT)n.
- To correlate subunit integrity with (dT)n binding ability.
Main Methods:
- Cesium sulfate density gradient centrifugation
- Sucrose gradient centrifugation
- Polyacrylamide gel electrophoresis (PAGE)
- Molecular weight distribution analysis
Main Results:
- Two distinct classes of SRRSV RNA subunits were identified based on (dT)n binding.
- 60-70% of purified subunits demonstrated the ability to bind (dT)n.
- Nonbinding RNA subunits were characterized as fragments lacking the riboadenylic acid (rA)n terminus, resulting from nucleolytic cleavage.
- Intact subunit RNA from early virus harvests showed a higher propensity for (dT)n binding.
Conclusions:
- The integrity of the riboadenylic acid (rA)n terminus is essential for (dT)n binding in SRRSV RNA subunits.
- Nucleolytic degradation leads to the formation of nonbinding RNA fragments.
- Early harvest virus provides a source of more intact RNA subunits with higher binding efficiency.