the enteropathogenic e. coli effector espf targets and disrupts the nucleolus by a process regulated by mitochondrial dysfunction大肠杆菌致肠病的效应espf目标和干扰的核仁过程由线粒体功能障碍.pdfVIP
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the enteropathogenic e. coli effector espf targets and disrupts the nucleolus by a process regulated by mitochondrial dysfunction大肠杆菌致肠病的效应espf目标和干扰的核仁过程由线粒体功能障碍
The Enteropathogenic E. coli Effector EspF Targets and
Disrupts the Nucleolus by a Process Regulated by
Mitochondrial Dysfunction
Paul Dean*, Jon A. Scott, Andrew A. Knox, Sabine Quitard, Nicholas J. Watkins, Brendan Kenny*
Institute for Cell and Molecular Biosciences, Medical School, University of Newcastle, Newcastle upon Tyne, United Kingdom
Abstract
The nucleolus is a multifunctional structure within the nucleus of eukaryotic cells and is the primary site of ribosome
biogenesis. Almost all viruses target and disrupt the nucleolus—a feature exclusive to this pathogen group. Here, using a
combination of bio-imaging, genetic and biochemical analyses, we demonstrate that the enteropathogenic E. coli (EPEC)
effector protein EspF specifically targets the nucleolus and disrupts a subset of nucleolar factors. Driven by a defined N-
terminal nucleolar targeting domain, EspF causes the complete loss from the nucleolus of nucleolin, the most abundant
nucleolar protein. We also show that other bacterial species disrupt the nucleolus, dependent on their ability to deliver
effector proteins into the host cell. Moreover, we uncover a novel regulatory mechanism whereby nucleolar targeting by
EspF is strictly controlled by EPEC’s manipulation of host mitochondria. Collectively, this work reveals that the nucleolus may
be a common feature of bacterial pathogenesis and demonstrates that a bacterial pathogen has evolved a highly
sophisticated mechanism to enable spatio-temporal control over its virulence proteins.
Citation: Dean P, Scott JA, Knox AA, Quitard S, Watkins NJ, et al. (2010) The Enteropathogenic E. coli Effector EspF Targets and Disrupts the Nucleolus by a
Process Regulated by Mitochondrial Dysfunction. PLoS Pathog 6(6): e1000961. doi:10.1371/journal.ppat.1000961
Editor: Guy Tran Van Nhieu, Institut Pasteur, France
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