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J Gen Virol 73 (1992), 1547-1551; DOI 10.1099/0022-1317-73-6-1547
© 1992 Society for General Microbiology

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Cell growth effects of Epstein—Barr virus leader protein

Gordon J. Allan, Gareth J. Inman, Bruce D. Parker{dagger}, David T. Rowe{ddagger}> and Paul J. Farrell

Ludwig Institute for Cancer Research, St Mary's Hospital Medical School, Norfolk Place, London W2 1PG, U.K.

B lymphoblastoid cell lines immortalized with P3HR1/633 Epstein—Barr virus (EBV), which has a deletion in the EBV nuclear antigen leader protein (EBNA-LP) gene, were transfected with a vector expressing wild-type EBNA-LP. The EBNA-LP trans-fectants grew out faster under G418 selection than control cells but expression of EBNA-LP made no significant difference to growth rate or saturation density of the resulting established cell lines. When the cells expressing EBNA-LP were allowed to grow to saturation and then diluted in fresh medium they underwent DNA synthesis more rapidly than control cultures.

{dagger} St Judes Children's Research Hospital, 332 North Lauderdale, Memphis, Tennessee 38101-0318, U.S.A.

{ddagger}> Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, U.S.A.

Received 4 December 1991; accepted 10 February 1992.


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