sgnp an essential stress granulenucleolar protein potentially involved in 5.8s rrna processingtransportsgnp必不可少的压力granulenucleolar蛋白可能参与5.8 s rrna processingtransport.pdfVIP
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sgnp an essential stress granulenucleolar protein potentially involved in 5.8s rrna processingtransportsgnp必不可少的压力granulenucleolar蛋白可能参与5.8 s rrna processingtransport
SGNP: An Essential Stress Granule/Nucleolar Protein
Potentially Involved in 5.8s rRNA Processing/Transport
Chun-Hong Zhu, Jinyong Kim, Jerry W. Shay, Woodring E. Wright*
Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America
Abstract
Background: Stress Granules (SG) are sites of accumulation of stalled initiation complexes that are induced following a
variety of cellular insults. In a genetic screen for factors involved in protecting human myoblasts from acute oxidative stress,
we identified a gene encoding a protein we designate SGNP (Stress Granule and Nucleolar Protein).
Methodology/Principal Findings: A gene-trap insertional mutagenesis screen produced one insertion that conferred
resistance to sodium arsenite. RT-PCR/39 RACE was used to identify the endogenous gene expressed as a GFP-fusion
transcript. SGNP is localized in both the cytoplasm and nucleolus and defines a non-nucleolar compartment containing 5.8S
rRNA, a component of the 60S ribosomal subunit. Under oxidative stress, SGNP nucleolar localization decreases and it
rapidly co-localizes with stress granules. The decrease in nucleolar SGNP following oxidative stress was accompanied by a
large increase in nucleolar 5.8S rRNA. Knockdown of SGNP with shRNA increased global mRNA translation but induced
growth arrest and cell death.
Conclusions: These results suggest that SGNP is an essential gene that may be involved in ribosomal biogenesis and
translational control in response to oxidative stress.
Citation: Zhu C-H, Kim J, Shay JW, Wright WE (2008) SGNP: An Essential Stress Granule/Nucleolar Protein Potentially Involved in 5.8s rRNA Processing/
Transport. PLoS ONE 3(11): e3716. doi:10.1371/journal.pone.0003716
Edito
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