Bangham C R, Daenke S, Phillips R E, Cruickshank J K, Bell J I
Institute for Molecular Medicine, John Radcliffe Hospital, Oxford, UK.
EMBO J. 1988 Dec 20;7(13):4179-84. doi: 10.1002/j.1460-2075.1988.tb03314.x.
Using oligonucleotide primers that hybridize to conserved sequences in the reverse transcriptase (RT) gene, we have amplified by the polymerase chain reaction three sequence variants of HTLV-I from the genomic DNA of five patients with tropical spastic paraparesis (TSP), and a fourth sequence variant from a healthy carrier of HTLV-I. These results unequivocally identify the retrovirus associated with TSP as HTLV-I and suggest that no sequence variant is uniquely responsible for the condition. The same primers served to amplify two novel single-copy endogenous retroviral RT sequences related to the exogenous mammalian leukaemia viruses: and three KpnI (LINE1) family DNA repeats. This strategy, combining the sensitivity of PCR with cross-reactive primers, may be useful in the search for known or novel retroviruses in other diseases of possible retroviral aetiology.
利用与逆转录酶(RT)基因保守序列杂交的寡核苷酸引物,我们通过聚合酶链反应从5例热带痉挛性截瘫(TSP)患者的基因组DNA中扩增出3种HTLV-I序列变体,从1例HTLV-I健康携带者中扩增出第4种序列变体。这些结果明确地将与TSP相关的逆转录病毒鉴定为HTLV-I,并表明没有单一的序列变体是导致该病的唯一原因。相同的引物还用于扩增与外源性哺乳动物白血病病毒相关的两种新的单拷贝内源性逆转录病毒RT序列,以及三种KpnI(LINE1)家族DNA重复序列。这种将PCR的敏感性与交叉反应引物相结合的策略,可能有助于在其他可能由逆转录病毒引起的疾病中寻找已知或新型逆转录病毒。