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利用基因组 DNA 的无细胞转录对古菌热休克调控因子 phr 的全基因组靶标进行鉴定。

Genome-wide identification of targets for the archaeal heat shock regulator phr by cell-free transcription of genomic DNA.

机构信息

Department of Microbiology, University of Regensburg, Universitaetsstr. 31, D-93053 Regensburg, Germany.

出版信息

J Bacteriol. 2010 Mar;192(5):1292-8. doi: 10.1128/JB.00924-09. Epub 2009 Dec 18.

Abstract

The hyperthermophilic archaeon Pyrococcus furiosus grows optimally near 100 degrees C and undergoes a heat shock response at 105 degrees C, mediated at least in part by the heat shock regulator Phr. Genes encoding a small heat shock protein (HSP20) and a member of the AAA(+) ATPase are the only known targets of the regulator, but a genetic mutant of Phr has yet to be characterized. We describe here an alternative approach for the identification of the regulon of Phr based on cell-free transcription of fragmented chromosomal DNA in the presence or absence of the regulator and hybridization of in vitro RNA to P. furiosus whole-genome microarrays. Our results confirmed the phr, the hsp20, and the aaa(+) ATPase genes as targets of Phr and also identified six additional open reading frames, PF0624, PF1042, PF1291, PF1292, PF1488, and PF1616, as Phr-responsive genes, which include that encoding di-myo-inositol phosphate synthase. Transcription of the identified novel genes was inhibited by Phr in standard transcription assays, and the novel consensus sequence 5'-TTTAnnnACnnnnnGTnAnnAAAA-3' (uppercase letters denote a high conservation of the bases) was inferred from our data as the Phr recognition motif. Mutational evidence for the significance of this sequence as Phr recognition was provided in DNA-binding experiments.

摘要

嗜热古菌 Pyrococcus furiosus 在接近 100°C 的温度下最佳生长,并在 105°C 时经历热休克反应,至少部分由热休克调节剂 Phr 介导。编码小热休克蛋白 (HSP20) 和 AAA(+)ATP 酶的基因是该调节剂的唯一已知靶标,但 Phr 的遗传突变体尚未得到表征。我们在这里描述了一种替代方法,用于基于存在或不存在调节剂的情况下细胞游离转录断裂的染色体 DNA,并将体外 RNA 杂交到 P. furiosus 全基因组微阵列,来鉴定 Phr 的调控组。我们的结果证实了 phr、hsp20 和 aaa(+)ATP 酶基因是 Phr 的靶标,还鉴定了另外六个开放阅读框,PF0624、PF1042、PF1291、PF1292、PF1488 和 PF1616,作为 Phr 反应基因,其中包括编码二肌醇磷酸合酶的基因。在标准转录测定中,鉴定的新基因的转录被 Phr 抑制,并且从我们的数据中推断出新颖的共有序列 5'-TTTAnnnACnnnnnGTnAnnAAAA-3'(大写字母表示碱基的高度保守)作为 Phr 识别基序。该序列作为 Phr 识别的重要性的突变证据在 DNA 结合实验中提供。

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