Goding C R, O'Hare P
Marie Curie Research Institute, The Chart, Oxted, Surrey, United Kingdom.
Virology. 1989 Dec;173(2):363-7. doi: 10.1016/0042-6822(89)90548-5.
The transcriptional status of a given viral or cellular gene is determined both by the availability of functional transcription factors and by the combination and spatial arrangement of the cis-acting elements to which they bind. While differential gene expression can be achieved to some extent by the interaction of different factors with different genes it is clear that in some cases the same factor is required for the regulation of genes that are not coordinately expressed. How a transcription factor achieves selective function in the absence of selective binding is a question that remains largely unanswered. The recent advances in understanding how both protein-protein and protein-DNA interactions are required to mediate the induction of herpes simplex virus immediate early (HSV IE) gene expression have highlighted a novel mechanism for combinatorial control of transcription which has significant implications for the differential control of cellular gene expression.
特定病毒或细胞基因的转录状态既取决于功能性转录因子的可获得性,也取决于它们所结合的顺式作用元件的组合及空间排列。虽然不同因子与不同基因的相互作用在一定程度上可实现基因的差异表达,但很明显,在某些情况下,调控非协同表达的基因需要相同的因子。转录因子在没有选择性结合的情况下如何实现选择性功能,这一问题在很大程度上仍未得到解答。最近在理解介导单纯疱疹病毒立即早期(HSV IE)基因表达诱导所需的蛋白质 - 蛋白质和蛋白质 - DNA相互作用方面取得的进展,突出了一种转录组合控制的新机制,这对细胞基因表达的差异控制具有重要意义。