Jenkins N A, Copeland N G
Cell. 1985 Dec;43(3 Pt 2):811-9. doi: 10.1016/0092-8674(85)90254-5.
RF/J mice carry three endogenous ecotropic murine leukemia proviruses designated Emv-1, Emv-16, and Emv-17. Two of these proviruses, Emv-16 and Emv-17, are tightly linked and segregate with the high viremia phenotype in backcrossed mice. During the derivation of an SWR/J strain congenic for Emv-16 and Emv-17, we found that many of the progeny derived from female virus carriers acquired new germline ecotropic proviruses. Additional genetic crosses suggested that these proviruses are acquired early in development by virus infection and that this strain combination is particularly susceptible to these events. The frequency of proviral acquisition was only about 10-fold lower than the frequency of P element acquisition in dysgenic crosses of Drosophila melanogaster. Since virus integration in these hybrids occurs at many different sites, these types of hybrids may ultimately be useful for generating virally induced mutations that are amenable to study at the molecular level.
RF/J小鼠携带三种内源性亲嗜性鼠白血病前病毒,分别命名为Emv - 1、Emv - 16和Emv - 17。其中两种前病毒,Emv - 16和Emv - 17,紧密连锁,并在回交小鼠中与高病毒血症表型一起分离。在培育携带Emv - 16和Emv - 17的SWR/J品系同源基因时,我们发现许多来自雌性病毒携带者的后代获得了新的种系亲嗜性前病毒。进一步的遗传杂交表明,这些前病毒是在发育早期通过病毒感染获得的,并且这种品系组合对这些事件特别敏感。前病毒获得的频率仅比黑腹果蝇发育不全杂交中P因子获得的频率低约10倍。由于这些杂种中的病毒整合发生在许多不同的位点,这些类型的杂种最终可能有助于产生适合在分子水平上进行研究的病毒诱导突变。