Biological activity of the intact and cleaved DNA of the simian adenovirus 7

Insights

Deproteinized simian adenovirus 7 (SA 7) DNA shows transforming and tumorigenic activity. However, its infectiousness is reduced when complexed with terminal protein (TP), despite enhanced tumorigenicity upon DNA cleavage.

Area of Science:

  • Molecular Biology
  • Virology
  • Oncology

Background:

  • Simian adenovirus 7 (SA 7) is a virus known to cause tumors.
  • The role of viral DNA and associated proteins in oncogenesis is a key area of research.

Purpose of the Study:

  • To investigate the transforming and tumorigenic potential of SA 7 DNA and its complex with terminal protein (TP).
  • To determine the influence of DNA cleavage by endonucleases on SA 7's oncogenic activity and infectivity.

Main Methods:

  • Deproteinization of SA 7 DNA.
  • Formation of SA 7 DNA-TP complexes.
  • Infectivity assays in monkey kidney cells.
  • Tumorigenicity assays in cell cultures.
  • Restriction endonuclease digestion of SA 7 DNA.

Main Results:

  • Deproteinized SA 7 DNA exhibited transforming and tumorigenic activity.
  • SA 7 DNA-TP complex lost transforming and tumorigenic activity but showed 30-50 times higher infectious titers.
  • DNA cleavage enhanced tumorigenic potential of pure DNA, reduced infectivity, and did not restore transformation capacity to the DNA-TP complex.
  • The oncogene was localized to the left terminal fragment (minimal size 4.3x10^6 D with R.Sal I).
  • Tumorigenic activity decreased with increasing size of the oncogene-containing DNA fragment.

Conclusions:

  • Terminal protein (TP) inhibits the transforming and tumorigenic activity of simian adenovirus 7 (SA 7) DNA.
  • Cleavage of SA 7 DNA by specific endonucleases can modulate its oncogenic potential and infectivity.
  • The oncogene responsible for tumorigenicity is located in the left terminal region of the SA 7 genome.

Related Concept Videos