Analysis of Sequences of Simian Adenovirus SA7 (C8) DNA in Transformed Rat Cells and Hamster Tumour Cells

The D.I. Ivanovsky Institute of Virology, Academy of Medical Sciences of the U.S.S.R., Moscow 123098, U.S.S.R. Different methods of molecular hybridization were used to study DNA sequences of the highly oncogenic simian adenovirus SA7 (C8) present in the genomes of two transformed rat cell lines and...

Full description

Saved in:
Bibliographic Details
Published in:Journal of general virology Vol. 64; no. 6; pp. 1381 - 1386
Main Authors: Gartel, A. L, Chaplygina, N. M, Ponomareva, T. I, Tiunnikov, G. I, Dreizin, R. S, Tikchonenko, T. I
Format: Journal Article
Language:English
Published: England Soc General Microbiol 01-06-1983
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The D.I. Ivanovsky Institute of Virology, Academy of Medical Sciences of the U.S.S.R., Moscow 123098, U.S.S.R. Different methods of molecular hybridization were used to study DNA sequences of the highly oncogenic simian adenovirus SA7 (C8) present in the genomes of two transformed rat cell lines and in cells from three hamster tumours induced by adenovirus SA7. The entire DNA or the left-hand terminal Sal I C fragment (19.5% of the genome) were employed. All cell lines retained an intact left-hand region of the SA7 genome (0 to 12.4 map units). The blot hybridization technique failed to detect any site specificity of integration of SA7 DNA into the cell genome. In all cell lines the expression of the Bgl II D fragment (1.8 to 10 map units) of SA7 DNA was observed. As judged by the patterns of integration of virus sequences into the cell genome, the highly oncogenic simian adenovirus SA7 (C8) is similar to the non-oncogenic human adenoviruses of group C, and is different from the highly oncogenic human adenovirus type 12. Keywords: adenovirus, SA7, transformation, DNA integration Received 29 September 1982; accepted 6 January 1983.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-64-6-1381