Chaudhary S, Brou C, Valentin M E, Burton N, Tora L, Chambon P, Davidson I
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génétique de l'INSERM, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
Mol Cell Biol. 1994 Aug;14(8):5290-9. doi: 10.1128/mcb.14.8.5290-5299.1994.
Transcription in HeLa cell extracts in vitro was stimulated 8- to 10-fold by a recombinant chimera, GAL-TEF-1, consisting of the DNA-binding domain of GAL4 and the activation function of the HeLa cell activator TEF-1. In contrast, only a 2- to 3-fold stimulation was obtained with GAL-TEF-1 in extracts from BJA-B lymphoid cells. Stimulation by GAL-TEF-1 in BJA-B extracts was dramatically increased by the addition of immunopurified HeLa cell TFIID, suggesting that BJA-B TFIID lacks or contains lower quantities of a TATA-binding-protein-associated factor(s) required for the activity of the TEF-1 activation function. However, chromatography, immunopurification, and transcriptional reconstitution experiments indicated that BJA-B extracts did not lack the previously identified TATA-binding-protein-associated factors required for TEF-1 activity but rather contained a negatively acting factor(s) which inhibited transactivation by GAL-TEF-1. These results indicate that the relative lack of activity of the TEF-1 activation function in vitro in BJA-B cell extracts does not result from the absence of positively acting factors from the presence of a cell-specific negatively acting factor(s).
在体外,由GAL4的DNA结合结构域和HeLa细胞激活因子TEF-1的激活功能组成的重组嵌合体GAL-TEF-1可将HeLa细胞提取物中的转录刺激8至10倍。相比之下,在BJA-B淋巴细胞提取物中,GAL-TEF-1只能产生2至3倍的刺激。添加免疫纯化的HeLa细胞TFIID后,BJA-B提取物中GAL-TEF-1的刺激作用显著增强,这表明BJA-B TFIID缺乏或含有较低量的TEF-1激活功能活性所需的TATA结合蛋白相关因子。然而,色谱分析、免疫纯化和转录重组实验表明,BJA-B提取物并不缺乏先前鉴定的TEF-1活性所需的TATA结合蛋白相关因子,而是含有一种负性作用因子,该因子抑制了GAL-TEF-1的反式激活作用。这些结果表明,BJA-B细胞提取物中TEF-1激活功能在体外相对缺乏活性,并非是由于缺乏正性作用因子,而是由于存在细胞特异性负性作用因子。