Fromental C, Kanno M, Nomiyama H, Chambon P
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Faculté de Médecine, Strasbourg, France.
Cell. 1988 Sep 23;54(7):943-53. doi: 10.1016/0092-8674(88)90109-2.
We have investigated the cell-specific activity of the GT-IIC, GT-I, Sph-II, Sph-I, and octamer motifs of the SV40 enhancer in four cell lines (HeLa cells, MPC11 plasmocytoma B cells, and non-differentiated and retinoic acid-differentiated F9 embryonal carcinoma cells). Our present results reveal the existence of three classes of motifs that interact with cell-specific enhancer factors but that have no enhancer activity of their own: those (class A) that generate enhancer activity following oligomerization of tandem repeats of the motif; those (class B) that cannot enhance transcription when oligomerized as a tandem repeat but whose association with a second motif results in transcription activation after oligomerization; and those (class C) that exhibit enhancer activity when a single copy of the motif is oligomerized. Three levels of functional organization of enhancers can also be defined. The possible implications for enhancer functions are discussed.
我们研究了SV40增强子的GT-IIC、GT-I、Sph-II、Sph-I和八聚体基序在四种细胞系(HeLa细胞、MPC11浆细胞瘤B细胞以及未分化和视黄酸分化的F9胚胎癌细胞)中的细胞特异性活性。我们目前的结果揭示了三类与细胞特异性增强子因子相互作用但自身没有增强子活性的基序的存在:一类(A类)在基序串联重复寡聚化后产生增强子活性;一类(B类)作为串联重复寡聚化时不能增强转录,但与第二个基序结合后在寡聚化后导致转录激活;还有一类(C类)当基序的单拷贝寡聚化时表现出增强子活性。增强子的功能组织也可以定义为三个层次。文中讨论了这些结果对增强子功能的可能影响。