Abstract
TIA (T-cell intracellular antigens)-knockdown HeLa cells show an increase in ribosomes and translational machinery components. This increase correlates with specific changes in translationally up-regulated mRNAs involved in cell-cycle progression and DNA repair, as shown in polysomal profiling analysis. Our data support the hypothesis that a concerted activation of both global and selective translational rates leads to the transition to a more proliferative status in TIA-knockdown HeLa cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Gene Expression Profiling / methods*
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Genome-Wide Association Study / methods*
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HeLa Cells
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Humans
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Intracellular Fluid* / immunology
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Poly(A)-Binding Proteins / genetics
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Poly(A)-Binding Proteins / physiology*
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RNA-Binding Proteins / genetics
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RNA-Binding Proteins / physiology*
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T-Cell Intracellular Antigen-1
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T-Lymphocytes / chemistry
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T-Lymphocytes / immunology*
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Transcriptional Activation* / immunology
Substances
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Poly(A)-Binding Proteins
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RNA-Binding Proteins
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T-Cell Intracellular Antigen-1
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TIA1 protein, human
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TIAL1 protein, human