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转录激活因子的时空磷酸化调控柄杆菌中极特异性基因的表达。

Spatial and temporal phosphorylation of a transcriptional activator regulates pole-specific gene expression in Caulobacter.

作者信息

Wingrove J A, Mangan E K, Gober J W

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles 90024-1569.

出版信息

Genes Dev. 1993 Oct;7(10):1979-92. doi: 10.1101/gad.7.10.1979.

Abstract

Polar localization of proteins in the Caulobacter predivisional cell results in the formation of two distinct progeny cells, a motile swarmer cell and a sessile stalked cell. The transcription of several flagellar promoters is localized to the swarmer pole of the predivisional cell. We present evidence that the product of the flbD gene is the transcriptional activator of these promoters. We show that FlbD is distributed in all cell types and in both poles of the predivisional cell. We also demonstrate that FlbD can be phosphorylated, and that a FlbD kinase activity is under cell cycle control. Cells expressing a FlbD mutant that should activate transcription in the absence of phosphorylation, exhibited an alteration in the temporal pattern of flagellin transcription. Furthermore, predivisional cells expressing the mutant FlbD failed to polarly localize flagellin synthesis. We propose that the phosphorylation of FlbD is restricted to the swarmer compartment of the predivisional cell, and serves as the control point for regulating the spatial transcription of flagellar promoters.

摘要

蛋白质在柄杆菌属细胞分裂前细胞中的极性定位导致形成两种不同的子代细胞,即游动的游动细胞和固着的柄细胞。几个鞭毛启动子的转录定位于分裂前细胞的游动极。我们提供的证据表明,flbD基因的产物是这些启动子的转录激活因子。我们表明,FlbD分布于所有细胞类型以及分裂前细胞的两极。我们还证明FlbD可以被磷酸化,并且FlbD激酶活性受细胞周期控制。表达在无磷酸化情况下应激活转录的FlbD突变体的细胞,鞭毛蛋白转录的时间模式出现改变。此外,表达突变体FlbD的分裂前细胞未能将鞭毛蛋白合成极性定位。我们提出,FlbD的磷酸化局限于分裂前细胞的游动区室,并作为调节鞭毛启动子空间转录的控制点。

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