Gergely L, Luka J, Klein G
J Gen Virol. 1984 Nov;65 ( Pt 11):2043-8. doi: 10.1099/0022-1317-65-11-2043.
Epstein-Barr virus (EBV) nuclear antigen (EBNA) was purified from the Burkitt lymphoma line Raji and its EBV DNA-binding properties were characterized. EBNA binding protected fragments of about 30 bp of B95-8 cell-derived EBV DNA from an excess of DNase I. Human anti-EBNA antibodies prevented DNA binding. Purified extracts from EBNA-negative cells did not protect EBV DNA against DNase I digestion. Mapping of the EBV DNA fragments protected from endonuclease (EcoRI, HindIII, SalI) digestion revealed many binding sites. Similar results were obtained following mixing of crude cell extracts and HindIII-digested fragments of EBV DNA and subsequent immunoprecipitation of the EBNA-DNA complex. In experiments involving the analysis of EBV DNA, fragments were protected from DNase I digestion by purified EBNA.
从伯基特淋巴瘤细胞系Raji中纯化出爱泼斯坦-巴尔病毒(EBV)核抗原(EBNA),并对其EBV DNA结合特性进行了表征。EBNA结合可保护来自B95-8细胞系的EBV DNA约30 bp的片段免受过量脱氧核糖核酸酶I(DNase I)的作用。人抗EBNA抗体可阻止DNA结合。EBNA阴性细胞的纯化提取物不能保护EBV DNA免受DNase I消化。对免受核酸内切酶(EcoRI、HindIII、SalI)消化的EBV DNA片段进行定位,发现了许多结合位点。将粗细胞提取物与EBV DNA的HindIII消化片段混合,随后对EBNA-DNA复合物进行免疫沉淀,也得到了类似的结果。在涉及EBV DNA分析的实验中,纯化的EBNA可保护片段免受DNase I消化。