O'Neill R R, Khan A S, Hoggan M D, Hartley J W, Martin M A, Repaske R
J Virol. 1986 May;58(2):359-66. doi: 10.1128/JVI.58.2.359-366.1986.
We have derived hybridization probes from analogous 100-base-pair segments located within the N-terminal region of gp70 coding sequences which differentiate xenotropic from mink cell focus-forming (MCF)-related murine leukemia virus (MuLV) DNAs. The MCF probe annealed to the integrated proviruses of all six MCF MuLV isolates tested; the xenotropic probe hybridized to the DNAs of all four xenotropic proviral isolates examined. No cross-hybridization was observed, and neither probe reacted with the env segments of amphotropic or ecotropic MuLV DNAs. Southern blot analysis of HindIII- or EcoRI-digested genomic DNAs from a variety of inbred laboratory mice demonstrated the presence of more MCF- than xenotropic MuLV-related segments in every strain tested.
我们从位于gp70编码序列N端区域内类似的100个碱基对片段中获得了杂交探针,这些片段可区分嗜异源性与貂细胞集落形成(MCF)相关的鼠白血病病毒(MuLV)DNA。MCF探针与所测试的所有六种MCF MuLV分离株的整合前病毒退火;嗜异源性探针与所检测的所有四种嗜异源性前病毒分离株的DNA杂交。未观察到交叉杂交,且两种探针均不与双嗜性或亲嗜性MuLV DNA的env片段反应。对来自多种近交系实验小鼠的经HindIII或EcoRI消化的基因组DNA进行的Southern印迹分析表明,在每个测试品系中,与MCF相关的MuLV片段比与嗜异源性相关的片段更多。