Retroviral sequence located in border region of short unique region and short terminal repeat of Md5 strain of Marek's desease virus type 1
1998
Endoh, D. (Hokkaido Univ., Sapporo (Japan)) | Ito, M. | Cho, K.O. | Kon, Y. | Morimura, T. | Hayshi, M. | Kuwabara, M.
A 246-base pair (bp) retroviral sequence, which was homologous to a long terminal repeat of avian erythroblastosis virus (AEV), was detected and cloned from Md5 strain (Md5) of Marek's disease virus type 1 (MDV1) by representational difference analysis (RDA). The retroviral sequence was thought to be located in the border region of short unique region (Us) and short terminal repeat (TRs), but did not exist in the border region of Us and the inverted short repeat (IRs) of the Md5 genome. A cloned fragment of the US/TRs border region of the Md5 genome showed a construction of U-E'-R-U'-E-TRs with the regions designated as follows: E, expanded TRs reported by Jones et al.; E', a partial copy of the expanded TRs: R, the retroviral sequence detected in Md5 genome; U, TRs-end sequence of Us; U', a partial copy of TRs-end sequence of Us. The sequence unit indicated as E'-R-U' was thought to be heterogeneously repeated in the Md% genome. Since this retroviral sequence reportedly did not exist in the original stock of Md5, the retroviral sequence is thought to be inserted in the Md5 genome without experimental co-infection of avian cells with retrovirus and MDV1. These results suggest that RDA could be useful for the detection of retroviral sequences in the herpesvirus genome
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