Shaw S B, Rasmussen R D, McDonough S H, Staprans S I, Vacquier J P, Spector D H
J Virol. 1985 Sep;55(3):843-8. doi: 10.1128/JVI.55.3.843-848.1985.
Human cytomegalovirus (HCMV) cloned EcoRI fragments R and b hybridized strongly, under standard high-stringency conditions, to uninfected cellular DNA of human, murine, or sea urchin origin. Less hybridization was detected with fragments, A, C, E, WL(F), WN(H), I, M, O, P, Q, V, c, d, and e. Southern blot analysis of the HCMV-related human DNA localized the major sites of hybridization of HCMV EcoRI fragments R, b, and d to defined regions of the 28S rRNA gene.
人类巨细胞病毒(HCMV)克隆的EcoRI片段R和b在标准高严格条件下与人类、小鼠或海胆来源的未感染细胞DNA强烈杂交。片段A、C、E、WL(F)、WN(H)、I、M、O、P、Q、V、c、d和e的杂交较少。对与HCMV相关的人类DNA进行的Southern印迹分析将HCMV EcoRI片段R、b和d的主要杂交位点定位到28S rRNA基因的特定区域。