Molecular cloning of bovine leukemia virus DNA integrated into the bovine tumor cell genome |
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Authors: | N Sagata Y Ogawa J Kawamura M Onuma H Izawa Y Ikawa |
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Affiliation: | 1. Laboratory of Molecular Oncology, The Institute of Physical and Chemical Research, Wako, Saitama 351, Tel. (0484) 62-1111 Japan;2. Department of Viral Oncology, Cancer Institute, Toshima-ku, Tokyo 170, Tel. (03)918-0111 Japan;3. Department of Epizootiology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido 060 Japan Tel. (011) 711-2111 |
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Abstract: | The bovine leukemia virus (BLV) DNA harbored in the bovine tumor cell genome was cloned in lambda Charon 4A phage. Using either representative or 3' half-enriched BLV cDNA as a blot hybridization probe, clone lambda BLV-1 was shown to carry 9 kb of the BLV genome, flanked by cellular sequences at both ends. Restriction mapping with twelve endonucleases and hybridization of the DNA fragments to BLV cDNA representing a 3'-end portion of the viral genome revealed the presence and precise location of two long terminal repeats (LTRs) and virus-cell junctions. Thus, lambda BLV-1 appears to contain the complete BLV genome and flanking tumor cellular sequences. The restriction map of the cloned BLV proviral DNA closely resembles that previously reported for unintegrated linear proviral DNA, but differs significantly from that of the integrated provirus of another BLV isolate, the difference occurring preferentially in the putative gag and pol genes. |
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Keywords: | Recombinant DNA λCharon vector provirus restriction mapping LTR flanking cellular sequence genetic variation BLV bovine leukemia virus bp base pairs cDNA 3′ half-enriched cDNA 3′ end-enriched cDNA) EBL enzootic bovine leukosis EtBr ethidium bromide FLK fetal lamb kidney cell kb kilobase pairs LTR long terminal repeat |
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