Decrease of tyrosine-O-sulfate-containing proteins found in rat fibroblasts infected with Rous sarcoma virus or
Summary
Malignant transformation of rat fibroblasts by sarcoma viruses reduces protein tyrosine sulfation. This reduction was most pronounced in cells infected with Rous sarcoma virus and temperature-sensitive Fujinami sarcoma virus.
Area of Science:
- Biochemistry
- Cell Biology
- Oncology
Background:
- Tyrosine sulfation is a post-translational modification found in various proteins.
- Malignant transformation can alter protein modifications, impacting cellular function.
- Previous work suggested general sulfation changes in transformed tissues.
Purpose of the Study:
- To investigate the effect of sarcoma virus infection on tyrosine sulfation in rat fibroblasts.
- To compare sulfation levels in normal versus virally transformed cells.
- To examine the role of temperature-sensitive viral mutants in altering sulfation.
Main Methods:
- Incubation of rat fibroblasts (3Y1) with [35S]sulfate.
- Analysis of protein sulfation following Pronase hydrolysis.
- Comparison of sulfation in cells infected with Rous sarcoma virus and Fujinami sarcoma virus (including a temperature-sensitive mutant).
- Measurement of inorganic [35S]sulfate uptake by cells.
Main Results:
- Sarcoma virus infection led to a general reduction in protein tyrosine sulfation in fibroblasts.
- Permanently transformed fibroblasts showed the greatest reduction in sulfation.
- Temperature-sensitive Fujinami sarcoma virus-transformed cells exhibited reduced sulfation at the permissive temperature.
- Sulfate uptake was reduced in permanently infected cells but not significantly different in temperature-sensitive cells at varying temperatures.
- Fibronectin released from temperature-sensitive cells at the permissive temperature contained tyrosine O-sulfate.
Conclusions:
- Viral transformation significantly impacts protein tyrosine sulfation in fibroblasts.
- Tyrosine O-sulfation of fibronectin is observed in transformed cells.
- The findings suggest a link between malignant transformation and altered tyrosine sulfation patterns.
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