Conklin K F, Groudine M
Mol Cell Biol. 1986 Nov;6(11):3999-4007. doi: 10.1128/mcb.6.11.3999-4007.1986.
Retroviruses integrated at unique locations in the host genome can be expressed at different levels. We have analyzed the preintegration sites of three transcriptionally competent avian endogenous proviruses (evs) to determine whether the various levels of provirus expression correlate with their location in active or inactive regions of chromatin. Our results show that in three of four cell types, the chromatin conformation (as defined by relative nuclease sensitivity) of virus preintegration sites correlates with the level of expression of the resident provirus in ev+ cells: two inactive proviruses (ev-1 and ev-2) reside in nuclease-resistant chromatin domains and one active provirus (ev-3) resides in a nuclease-sensitive domain. Nuclear runoff transcription assays reveal that the preintegration sites of the active and inactive viruses are not transcribed. However, in erythrocytes of 15-day-old chicken embryos (15d RBCs), the structure and activity of the ev-3 provirus is independent of the conformation of its preintegration site. In this cell type, the ev-3 preintegration site is organized in a nuclease-resistant conformation, while the ev-3 provirus is in a nuclease-sensitive conformation and is transcribed. In addition, the nuclease sensitivity of host sequences adjacent to ev-3 is altered in ev-3+ 15d RBCs relative to that found in 15d RBCs that lack ev-3. These data suggest that the relationship between preintegration site structure and retrovirus expression is more complex than previously described.
整合于宿主基因组独特位置的逆转录病毒可在不同水平表达。我们分析了三种具有转录活性的禽内源性前病毒(evs)的整合前位点,以确定前病毒表达的不同水平是否与其在染色质活性或非活性区域的位置相关。我们的结果表明,在四种细胞类型中的三种里,病毒整合前位点的染色质构象(由相对核酸酶敏感性定义)与ev+细胞中常驻前病毒的表达水平相关:两种无活性的前病毒(ev-1和ev-2)位于核酸酶抗性染色质结构域,一种有活性的前病毒(ev-3)位于核酸酶敏感结构域。核转录分析表明,有活性和无活性病毒的整合前位点均不转录。然而,在15日龄鸡胚的红细胞(15d RBCs)中,ev-3前病毒的结构和活性与其整合前位点的构象无关。在这种细胞类型中,ev-3整合前位点呈核酸酶抗性构象,而ev-3前病毒呈核酸酶敏感构象并进行转录。此外,相对于缺乏ev-3的15d RBCs,ev-3 + 15d RBCs中与ev-3相邻的宿主序列的核酸酶敏感性发生了改变。这些数据表明,整合前位点结构与逆转录病毒表达之间的关系比先前描述的更为复杂。