Shimron F, Yagil G
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Int J Biol Macromol. 1993 Apr;15(2):89-95. doi: 10.1016/0141-8130(93)90003-5.
The de novo construction of defined nucleosomes from two DNA fragments of simian virus SV40 is described. One fragment spans the region containing the origin of replication of the virus from base -16 to base 161, a region which is nucleosome-free during virus replication. The other fragment, of 142 bp (1352 to 1493), is within the region coding for viral proteins VP2 and VP3, and serves for comparison. Both fragments form nucleosomes with similar efficiency when combined with histone cores as well as when exchanged with existing core particles. The DNase I digestion pattern and exonuclease III analysis both indicate that true nucleosome cores are formed, and that a prolonged tail is not protruding from the constructs. The efficient formation of a nucleosome core particle from the origin region of DNA implies that the absence of nucleosomes from this region during viral infection is not prescribed by the specific base sequence of origin DNA, and is therefore likely to be determined by non-histone nuclear factors associated with the SV40 replication process.
本文描述了利用猿猴病毒SV40的两个DNA片段从头构建特定核小体的过程。一个片段跨度为从碱基-16到碱基161的区域,该区域包含病毒的复制起点,在病毒复制过程中此区域无核小体。另一个片段为142bp(1352至1493),位于编码病毒蛋白VP2和VP3的区域内,用于对照。当与组蛋白核心结合以及与现有的核心颗粒交换时,这两个片段形成核小体的效率相似。DNase I消化模式和核酸外切酶III分析均表明形成了真正的核小体核心,且构建体中没有伸出延长的尾巴。从DNA的起始区域高效形成核小体核心颗粒意味着病毒感染期间该区域无核小体并非由起始DNA的特定碱基序列所决定,因此很可能是由与SV40复制过程相关的非组蛋白核因子所决定。