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An activation function in Pit-1 required selectively for synergistic transcription.

作者信息

Chang W, Zhou W, Theill L E, Baxter J D, Schaufele F

机构信息

Metabolic Research Unit, University of California, San Francisco, California 94143-0540, USA.

出版信息

J Biol Chem. 1996 Jul 26;271(30):17733-8. doi: 10.1074/jbc.271.30.17733.

Abstract

Synergistic transcription activation is a key component in the generation of the spectrum of eukaryotic promoter activities by a limited number of transcription factors. Various mechanisms could account for synergy, but a central question remains of whether synergism requires transcription factor functions that differ from those that direct independent activation. The rat growth hormone promoter is synergistically activated by the pituitary-specific transcription factor, Pit-1, and the thyroid hormone receptor (TR). Mutations that disrupted the previously described DNA binding and transcriptional activation domains of both Pit-1 and TR reduced Pit-1/TR synergy in parallel with their effects on the much weaker, independent Pit-1 and TR activations of the rat growth hormone promoter. Thus, Pit-1 and TR amplify each other's intrinsic activities. Mutations of Pit-1 that selectively inhibited synergism with the TR without affecting independent Pit-1 activity were also identified. Pit-1/TR synergy is therefore a consequence of a novel synergism-selective activity and synergism-independent Pit-1 and TR functions.

摘要

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