Bode J, Schlake T, Ríos-Ramírez M, Mielke C, Stengert M, Kay V, Klehr-Wirth D
Gesellschaft für Biotechnologische Forschung m.b.H., Braunschweig, Germany.
Int Rev Cytol. 1995;162A:389-454. doi: 10.1016/s0074-7696(08)61235-8.
The expression characteristics of the human interferon-beta gene, as part of a long stretch of genomic DNA, led to the discovery of the putative domain bordering elements. The chromatin structure of these elements and their surroundings was determined during the process of gene activation and correlated with their postulated functions. It is shown that these "scaffold-attached regions" (S/MAR elements) have some characteristics in common with and others distinct from enhancers with which they cooperate in various ways. Our model of S/MAR function will focus on their properties of mediating topological changes within the respective domain.
人类β-干扰素基因作为一段长基因组DNA的一部分,其表达特征导致了假定的结构域边界元件的发现。在基因激活过程中确定了这些元件及其周围环境的染色质结构,并将其与它们假定的功能相关联。结果表明,这些“支架附着区域”(S/MAR元件)具有一些与增强子相同的特征,也有一些不同的特征,它们以各种方式与增强子协同作用。我们的S/MAR功能模型将聚焦于它们在各自结构域内介导拓扑变化的特性。