Given D, Kieff E
J Virol. 1978 Nov;28(2):524-42. doi: 10.1128/JVI.28.2.524-542.1978.
The arrangement of EcoRI, Hsu I, and Sal I restriction enzyme sites in the DNA of the B95-8 and W91 isolates of Epstein-Barr virus (EBV) has been determined from the size of the single-enzyme-cleaved fragments and from blot hybridizations that identify which fragments cut from the DNA with one enzyme contain nucleotide sequences in common with fragments cut from the DNA with a second enzyme. The DNA of the B95-8 isolate was the prototype for this study. The data indicate that (i) approximately 95 X 10(6) to 100 X 10(6) daltons of EBV (B95-8) DNA is in a consistent and unique sequence arrangement. (ii) Both termini are variable in length. One end of the molecule after Hsu I endonuclease cleavage consists of approximately 3,000 base pairs, with as many as 10 additional 500-base pair segments. The opposite end of the molecule after Sal I endonuclease cleavage consists of approximately 1,500 base pairs, with as many as 10 additional 500-base pair segments. (iii) The opposite ends of the molecule contain homologous sequences. The high degree of homology between the opposite ends of the molecule and the similarity in size of the "additional" 500-base pair segments suggests that there are identical repeating units at both ends of the DNA. The arrangement of restriction endonuclease fragments of the DNA of the W91 isolate of EBV is similar to that of the B95-8 isolate and differs from the latter in the presence of approximately 7 X 10(6) daltons of "extra" DNA at a single site. Thus, the size of almost all EcoRI, Hsu I, and Sal I fragments of EBV (W91) DNA is identical to that of fragments of EBV (B95-8) DNA. A single EcoRI fragment, C, of EBV (W91) DNA is approximately 7 X 10(6) daltons larger than the corresponding EcoRI fragment of EBV (B95-8) DNA. Digestion of EBV (W91) DNA with Hsu I or Sal I restriction endonucleases produces two fragments (Hsu I D1 and D2 or Sal I G2 and G3) which differ in total size by approximately 7 X 10(6) daltons from the fragments of EBV (B95-8) DNA. Furthermore, the EcoRI, Hsu I, and Sal I fragments of EBV (W91) and (B95-8) DNAs, which are of similar molecular weight, have homologous nucleotide sequences. Moreover, the W91 fragments contain only sequences from a single region of the B95-8 genome. Two lines of evidence indicate that the "extra" sequences present in W91 EcoRI fragment C are viral DNA and not cellular. (i) The molecular weight of the "enlarged" EcoRI C fragment of EBV (W91) DNA is identical to that of the EcoRI C fragment of another isolate of EBV (Jijoye), (ii) The HR-1 clone of Jijoye has previously been shown to contain DNA which is not present in the B95-8 strain but is present in the EcoRI C and Hsu I D2 and D1 fragments of EBV (W91) DNA (N. Raab-Traub, R. Pritchett, and E. Kieff, J. Virol. 27:388-398, 1978).
通过单酶切片段的大小以及印迹杂交(该方法可鉴定用一种酶切割DNA产生的哪些片段含有与用另一种酶切割DNA产生的片段相同的核苷酸序列),已确定了爱泼斯坦-巴尔病毒(EBV)的B95-8和W91分离株DNA中EcoRI、Hsu I和Sal I限制性酶切位点的排列方式。B95-8分离株的DNA是本研究的原型。数据表明:(i)EBV(B95-8)DNA中约95×10⁶至100×10⁶道尔顿处于一致且独特的序列排列中。(ii)两个末端长度可变。Hsu I内切酶切割后分子的一端约由3000个碱基对组成,还有多达10个额外的500个碱基对片段。Sal I内切酶切割后分子的另一端约由1500个碱基对组成,还有多达10个额外的500个碱基对片段。(iii)分子的相对两端含有同源序列。分子相对两端的高度同源性以及“额外”的500个碱基对片段大小的相似性表明DNA两端存在相同的重复单元。EBV的W91分离株DNA的限制性内切酶片段排列与B95-8分离株相似,不同之处在于在单个位点存在约7×10⁶道尔顿的“额外”DNA。因此,EBV(W91)DNA的几乎所有EcoRI、Hsu I和Sal I片段的大小与EBV(B95-8)DNA片段的大小相同。EBV(W91)DNA的单个EcoRI片段C比EBV(B95-8)DNA的相应EcoRI片段大约7×10⁶道尔顿。用Hsu I或Sal I限制性内切酶消化EBV(W91)DNA会产生两个片段(Hsu I D1和D2或Sal I G2和G3),其总大小与EBV(B95-8)DNA的片段相差约7×10⁶道尔顿。此外,EBV(W91)和(B95-8)DNA中分子量相似的EcoRI、Hsu I和Sal I片段具有同源核苷酸序列。而且,W91片段仅包含来自B95-8基因组单个区域的序列。有两条证据表明W91 EcoRI片段C中存在的“额外”序列是病毒DNA而非细胞DNA。(i)EBV(W91)DNA“增大”的EcoRI C片段的分子量与EBV另一个分离株(Jijoye)的EcoRI C片段的分子量相同,(ii)之前已表明Jijoye的HR-1克隆含有B95-8菌株中不存在但存在于EBV(W91)DNA的EcoRI C以及Hsu I D2和D1片段中的DNA(N. Raab-Traub、R. Pritchett和E. Kieff,《病毒学杂志》27:388 - 398,1978年)。