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非洲爪蟾5S RNA基因特异性正转录因子的结构域。

Domains of the positive transcription factor specific for the Xenopus 5S RNA gene.

作者信息

Smith D R, Jackson I J, Brown D D

出版信息

Cell. 1984 Jun;37(2):645-52. doi: 10.1016/0092-8674(84)90396-9.

Abstract

The 40 kd positive transcription factor that interacts with the 50 nucleotide internal control region of 5S ribosomal RNA genes in Xenopus can be subdivided into three functional domains by proteolytic cleavage. At one end of the protein is a 10 kd domain that is required for efficient RNA transcription but not for binding to the DNA. This adjoins a second domain that binds to the 5' end of the internal control region, a region of the DNA known to contribute only weakly to binding the protein but one that is essential for RNA transcription. The removal of both of these protein domains leaves a half of the protein that binds only to the 3' side of the control region and is inactive in promoting transcription. Quantitative DNA binding and in vitro transcription experiments show that only a single molecule of 40 kd factor binds to the internal control region, and that this stoichiometry is sufficient to give maximal stimulation of 5S RNA transcription in a reconstituted system. Consideration of the essential DNA contact points of the factor, taken together with the constraints imposed by a 1:1 protein to DNA stoichiometry permit the linear projection of the extended protein molecule onto its binding site along the internal control region of the 5S RNA gene.

摘要

在非洲爪蟾中,与5S核糖体RNA基因的50个核苷酸内部控制区相互作用的40kd正转录因子可通过蛋白水解切割细分为三个功能结构域。在蛋白质的一端是一个10kd的结构域,它是高效RNA转录所必需的,但不是与DNA结合所必需的。这个结构域毗邻第二个结构域,该结构域与内部控制区的5'端结合,已知该DNA区域对蛋白质结合的贡献很小,但对RNA转录至关重要。去除这两个蛋白质结构域后,剩下的一半蛋白质仅与控制区的3'侧结合,并且在促进转录方面无活性。定量DNA结合和体外转录实验表明,只有一个40kd因子分子与内部控制区结合,并且这种化学计量足以在重组系统中最大程度地刺激5S RNA转录。考虑到该因子的基本DNA接触点,再结合1:1蛋白质与DNA化学计量所施加的限制,可以将延伸的蛋白质分子沿5S RNA基因的内部控制区线性投影到其结合位点上。

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