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伯克霍尔德菌假鼻疽亚种真核转录共激活因子PC4同源物的结构分析与敲除

Structural analysis and knock-out of a Burkholderia pseudomallei homolog of the eukaryotic transcription coactivator PC4.

作者信息

Werten Sebastiaan, Kohler Christian, Bayer Niklas Johannes, Steinmetz Ivo, Hinrichs Winfried

机构信息

Department of Molecular Structural Biology, Institute for Biochemistry, University of Greifswald, Felix-Hausdorff-Strasse 4, D-17487 Greifswald, Germany.

Friedrich Loeffler Institute for Medical Microbiology, Martin-Luther-Strasse 6, D-17475 Greifswald, Germany.

出版信息

Gene. 2016 Feb 15;577(2):140-7. doi: 10.1016/j.gene.2015.11.037. Epub 2015 Nov 25.

Abstract

Homologs of the eukaryotic transcription coactivator PC4, which also functions in DNA repair and oxidative stress, were recently identified in prokaryotes. Crystallographic analysis of BPSL1147, a putative homolog from the pathogen Burkholderia pseudomallei K96243, reveals a highly conserved core structure and suggests a nucleic acid binding mode similar to that of PC4. Knock-out and complementation experiments do not reveal distinguishing phenotypes under normal growth conditions or in the presence of H2O2, arguing against a critical role in repair or the oxidative stress response of Burkholderia. These results may reflect redundancy or point at a bacteriophage origin of Burkholderia PC4 homologs.

摘要

真核转录共激活因子PC4的同源物在原核生物中也发挥着DNA修复和氧化应激的作用,最近在原核生物中被发现。对来自病原体伯克霍尔德菌假鼻疽亚种K96243的假定同源物BPSL1147进行晶体学分析,揭示了一种高度保守的核心结构,并表明其核酸结合模式与PC4相似。敲除和互补实验未发现在正常生长条件下或存在过氧化氢时的明显表型差异,这表明其在伯克霍尔德菌的修复或氧化应激反应中不发挥关键作用。这些结果可能反映了冗余性,也可能表明伯克霍尔德菌PC4同源物起源于噬菌体。

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