## Abstract Human lymphoblastoid lines of various origins which harbour Epstein‐Barr virus (EBV)‐specific nucleic acid were re‐exposed to EBV. Following infection, cells of the non‐virus‐producing lines, Raji and S 95, predominantly synthesized EBV‐specific early antigens (EA), whereas only a small
Non-random integration of epstein-barr virus in lymphoblastoid cell lines
✍ Scribed by Valia S. Lestou; Marc De Braekeleer; Sabine Strehl; German Ott; Helmut Gadner; Peter F. Ambros
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 823 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1045-2257
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✦ Synopsis
In order t o examine the role of Epstein-Barr virus (EBV) in the immortalization of human B lymphocytes and in the pathogenesis of lymphoid malignancies, we investigated whether the EBV integration into the human genome is randomly distributed or whether the virus integrates preferentially at certain sites. Twelve in vitro immortalized human lymphoblastoid cell lines (LCLs), two in vivo infected LCLs, and one Burkitt's lymphoma cell line (EB2) were examined by non-radioactive in situ hybridization (ISH) with a biotinylated EBV probe. Recurrent hybridization sites were detected in all 15 cell lines. The chromosomes frequently carrying the EBV genome were chromosomes I, 2,4, and 5. In more than 70 chromosomal bands, a greater number of integration sites than expected was found (p < 0.05). Approximately half of these bands were involved in the majority of the cell lines (for example, I p3 I, I q43,2p22, 3q28,4q I 3,5p I4,Sq 12. and I I p 15) whereby band 5p I 4 was involved in all LCLs analyzed. Virtually no viral integrations were found on the sex chromosomes (X, Y). The majority of the EBV integrations was found in G-band-positive material (p < 0.0001). Thus, our findings clearly show that EBV integrates into the human genome in a non-random manner.
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