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首页> 外文期刊>Biochemical and Biophysical Research Communications >Characterization of the specific interaction between archaeal FHA domain-containing protein and the promoter of a flagellar-like gene-cluster and its regulation by phosphorylation.
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Characterization of the specific interaction between archaeal FHA domain-containing protein and the promoter of a flagellar-like gene-cluster and its regulation by phosphorylation.

机译:表征古细菌FHA结构域的蛋白质和鞭毛状基因簇的启动子之间的特异性相互作用及其通过磷酸化的调控。

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摘要

The mechanism and target genes of regulation by Forkhead (FHA) domain-containing transcription factors have not yet been documented in Archaea. In this study, using a bacterial one-hybrid technique, we successfully screened and identified for the first time a target gene regulated by ST0829, an FHA domain-containing potential transcriptional factor in the hyperthermophilic archaeon Sulfolobus tokodaii. We show that ST0829 could specifically bind to the promoter region of ST2519p, the archaeal flagellar protein-encoding operon (including FlaG, FlaF, FlaH, FlaI, and FlaJ) by using both in vitro electrophoretic mobility shift assay and surface plasmon resonance experiments, and invivo chromatin immunoprecipitation assays. Furthermore, phosphorylation of the FHA domain-containing protein was found to negatively regulate its specific DNA-binding activity. The interaction between ST0829 and ST2519p could be inhibited by wild-type Ser/Thr protein kinase ST1565, but was not significantly affected by its mutant variant ST1565-K166A that lacks kinase activity. These findings not only increase our knowledge about the function of an archaeal FHA domain-containing regulator but also offer important insights for further understanding the signaling mechanism of environmental adaptation in archaea.
机译:尚未在古细菌中记载由含Forkhead(FHA)域的转录因子调控的机制和靶基因。在这项研究中,我们使用细菌单杂交技术成功地筛选并首次鉴定了由ST0829调控的靶基因,ST0829是超嗜热古生硫磺鸟(Sulfolobus tokodaii)中含有FHA结构域的潜在转录因子。我们展示了ST0829可以通过使用体外电泳迁移率迁移分析和表面等离振子共振实验特异性结合ST2519p的启动子区域,古细菌鞭毛蛋白编码操纵子(包括FlaG,FlaF,FlaH,FlaI和FlaJ),并且体内染色质免疫沉淀测定。此外,发现含FHA结构域的蛋白质的磷酸化负调控其特异性DNA结合活性。野生型Ser / Thr蛋白激酶ST1565可以抑制ST0829和ST2519p之间的相互作用,但不受缺乏激酶活性的突变变体ST1565-K166A的影响不大。这些发现不仅增加了我们对含古细菌FHA结构域调节剂功能的了解,而且为进一步理解古细菌环境适应的信号传导机制提供了重要的见识。

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