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Abortive expression of the epstein‐barr virus (EBV) cycle in a variety of EBV DNA‐containing cell lines, as reflected by nucleic acid hybridization In situ
Author(s) -
Moar Martin H.,
Klein George
Publication year - 1979
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910240524
Subject(s) - epstein–barr virus , biology , virus , antigen , dna , microbiology and biotechnology , virology , immunofluorescence , capsid , in situ hybridization , cell culture , nucleic acid , antibody , gene expression , gene , immunology , genetics
A variety of Epstein‐Barr virus (EBV) DNA‐containing cell lines have been tested for the expression of the EBV‐associated antigens EBNA (nuclear antigen), EA (early antigen), and VCA (viral capsid antigen), and for the presence of cells containing disproportionate amounts of EBV DNA. The antigen tests utilized immunofluorescence and 125 I‐labelled antibodies combined with auto‐radiography. EBV‐DNA was detected by in situ hybridization with 3 H‐labelled EBV RNA complementary to P3HR‐1 EBV DNA (P‐EBVcRNA). The P‐EBV cRNA has been shown to represent the majority of the P3HR‐1 EBV DNA sequences. It was concluded that EBV DNA‐containing cell lines can be divided into those that express only EBNA, those that express EBNA and EA and those that express EBNA, EA and VCA and also contain cells that undergo disproportionate EBV DNA synthesis. Consequently, in some cell lines there is an abortive expression of the EBV cycle in that some cells spontaneously express EA but fail to continue further to viral DNA synthesis. A similar pattern can be found after experimental induction of the EBV cycle, suggesting that related mechanisms govern the spontaneous expression of the EBV cycle and the extent of its inducibility.
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