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发育周期早期和中期合成的鹦鹉热衣原体DNA结合蛋白(EUO)的特性分析。

Characterization of a Chlamydia psittaci DNA binding protein (EUO) synthesized during the early and middle phases of the developmental cycle.

作者信息

Zhang L, Douglas A L, Hatch T P

机构信息

Department of Microbiology and Immunology, University of Tennessee, Memphis 38163, USA.

出版信息

Infect Immun. 1998 Mar;66(3):1167-73. doi: 10.1128/IAI.66.3.1167-1173.1998.

Abstract

The EUO gene (for early upstream open reading frame) of Chlamydia psittaci was previously found to be transcribed better at 1 than at 24 h postinfection. We found that the EUO gene encodes a minor protein that is expressed within 1 h of infection of host cells with C. psittaci 6BC but that protein quantity peaks during the logarithmic growth phase of reticulate bodies (RBs), declines late in the infection (after 20 h) when RBs reorganize into elementary bodies (EBs), and is absent in infectious EBs. EUO protein lacks homology to known proteins but does contain a putative helix-turn-helix motif. We found that recombinant EUO binds to DNA in vitro with a relatively broad specificity. Using the bp -200 to +67 promoter region of the cysteine-rich envelope protein (crp) operon as a model, we show that EUO protein preferentially binds to AT-rich sequences and protects crp DNA from DNase I from approximately bp -60 to -9. We also found that native EUO protein in extracts of RBs binds to the promoter region of the crp operon, demonstrating that the DNA binding property of EUO protein is not an artifact of recombinant methods. Although EUO protein appears to bind to the crp operon with high affinity in vitro (Kd of about 15 nM), it is not known whether the protein binds the crp DNA in vivo.

摘要

鹦鹉热衣原体的EUO基因(早期上游开放阅读框)先前被发现,在感染后1小时的转录情况优于24小时。我们发现,EUO基因编码一种次要蛋白,该蛋白在鹦鹉热衣原体6BC感染宿主细胞后1小时内表达,但蛋白量在网状体(RB)的对数生长期达到峰值,在感染后期(20小时后)当RB重组为原体(EB)时下降,且在传染性EB中不存在。EUO蛋白与已知蛋白缺乏同源性,但确实含有一个假定的螺旋-转角-螺旋基序。我们发现重组EUO在体外以相对广泛的特异性与DNA结合。以富含半胱氨酸的包膜蛋白(crp)操纵子的-200至+67 bp启动子区域为模型,我们表明EUO蛋白优先结合富含AT的序列,并保护crp DNA免受DNase I从约-60至-9 bp的切割。我们还发现RB提取物中的天然EUO蛋白与crp操纵子的启动子区域结合,表明EUO蛋白的DNA结合特性不是重组方法的假象。尽管EUO蛋白在体外似乎以高亲和力结合crp操纵子(Kd约为15 nM),但尚不清楚该蛋白在体内是否结合crp DNA。

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