Fleckenstein B, Müller I, Collins J
Gene. 1982 Apr;18(1):39-46. doi: 10.1016/0378-1119(82)90054-3.
Purified virion DNA (155 X 10(6) Mr) of human cytomegalovirus (CMV) strain Ad169 was partially cleaved with restriction endonucleases HindIII and EcoRI and cloned in the respective cleavage sites of cosmid pHC79. A complete gene library was established in a set of clones containing the viral DNA in long overlapping segments. Restriction maps for HindIII (29 fragments) and EcoRI (36 fragments) were constructed from the linkage of cosmid-cloned fragments, from double digestions of cloned DNA, and from blot hybridization of labeled cloned viral DNA with restriction fragments of virion DNA and singly or doubly cleaved cosmid clones.
人巨细胞病毒(CMV)Ad169株的纯化病毒体DNA(155×10⁶道尔顿)用限制性内切酶HindIII和EcoRI进行部分切割,并克隆到黏粒pHC79的相应切割位点。在一组包含长重叠片段病毒DNA的克隆中建立了一个完整的基因文库。通过黏粒克隆片段的连接、克隆DNA的双酶切以及标记的克隆病毒DNA与病毒体DNA的限制性片段和单切或双切黏粒克隆的印迹杂交,构建了HindIII(29个片段)和EcoRI(36个片段)的限制性图谱。