Pritchett R F, Hayward S D, Kieff E D
J Virol. 1975 Mar;15(3):556-9. doi: 10.1128/JVI.15.3.556-559.1975.
We have compared the properties of the DNA of Epstein-Barr virus (EBV) purified from HR-1 (EBV HR-1 DNA) and B95-8 (EBV B95-8 DNA) continuous lymphoblast cultures. Our data indicate that (i) the S suc of native EBV DNA relative to T4D DNA is 55S. Using the modified Burgi-Hershey relationship (5), we estimate the molecular weight of native EBV DNA is 101 (plus or minus the molecular weight of native FBV DNA by measurement of the length of 3) times 106. Estimation of the molecule relative to form II PM2 DNA yields a value of 105 (plus or minus 3) times 106. (ii) After alkali denaturation, less than 50% of EBV DNA sediments as a single band in alkaline sucrose gradients in the region expected for DNA of 50 times 406 daltons. (iii) Intact EBV HR-1 and EBV B 95-8 DNAs band at 1.718 g/cm3 and a smaller band (approximately 25% of the DNA) AT 1.720 G/CM3. (IV) EBV HR-1 DNA possesses greater than 97% of the sequences of EBV B95-8 DNA. Hybrid DNA molecules formed between (3H)EBV HR-1 DNA and EBV HR-1 DNA or EBV B95-8 DNA had identical thermal stability. EBV B95-8 DNA lacks approximately 15% of the DNA sequences of EBV HR-1 DNA. We interpret these data to mean that EBV B95-8 is derived from a parental EBV through loss of genetic complexity. This defect may be linked to the ability of EBV B95-8 to "transform" lymphocytes invitro.
我们比较了从HR - 1连续淋巴母细胞培养物中纯化得到的爱泼斯坦 - 巴尔病毒(EBV)DNA(EBV HR - 1 DNA)和从B95 - 8连续淋巴母细胞培养物中纯化得到的EBV DNA(EBV B95 - 8 DNA)的特性。我们的数据表明:(i)天然EBV DNA相对于T4D DNA的S suc为55S。利用修正后的Burgi - Hershey关系(5),我们估计天然EBV DNA的分子量为101(正负通过测量3的长度得到的天然FBV DNA的分子量)×10⁶。相对于II型PM2 DNA估计该分子的值为105(正负3)×10⁶。(ii)碱变性后,在碱性蔗糖梯度中,小于50%的EBV DNA在预期的50×406道尔顿DNA区域以单一条带形式沉降。(iii)完整的EBV HR - 1和EBV B 95 - 8 DNA在1.718 g/cm³处形成条带,还有一条较小的条带(约占DNA的25%)在1.720 g/cm³处。(iv)EBV HR - 1 DNA拥有超过97%的EBV B95 - 8 DNA序列。(³H)EBV HR - 1 DNA与EBV HR - 1 DNA或EBV B95 - 8 DNA形成的杂交DNA分子具有相同的热稳定性。EBV B95 - 8 DNA缺少约15%的EBV HR - 1 DNA序列。我们将这些数据解释为意味着EBV B95 - 8是通过遗传复杂性的丧失从亲本EBV衍生而来。这种缺陷可能与EBV B95 - 8在体外“转化”淋巴细胞的能力有关。