Abstract
The DNA damage response involves a complex network of processes that detect and repair DNA damage. Here we show that miRNA biogenesis is globally induced upon DNA damage in an ATM-dependent manner. About one-fourth of miRNAs are significantly upregulated after DNA damage, while loss of ATM abolishes their induction. KH-type splicing regulatory protein (KSRP) is a key player that translates DNA damage signaling to miRNA biogenesis. The ATM kinase directly binds to and phosphorylates KSRP, leading to enhanced interaction between KSRP and pri-miRNAs and increased KSRP activity in miRNA processing. Mutations of the ATM phosphorylation sites of KSRP impaired its activity in regulating miRNAs. These findings reveal a mechanism by which DNA damage signaling is linked to miRNA biogenesis.
Copyright © 2011 Elsevier Inc. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Ataxia Telangiectasia Mutated Proteins
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Cell Cycle Proteins / metabolism*
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DNA Damage / physiology*
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DNA-Binding Proteins / metabolism*
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Humans
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Mice
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MicroRNAs / metabolism*
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Phosphorylation
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Protein Serine-Threonine Kinases / metabolism*
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RNA Interference
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RNA-Binding Proteins / genetics
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RNA-Binding Proteins / metabolism
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Signal Transduction
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Trans-Activators / genetics
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Trans-Activators / metabolism
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Transfection
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Tumor Cells, Cultured
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Tumor Suppressor Proteins / metabolism*
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Up-Regulation
Substances
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Cell Cycle Proteins
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DNA-Binding Proteins
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KHSRP protein, human
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Khsrp protein, mouse
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MicroRNAs
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RNA-Binding Proteins
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Trans-Activators
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Tumor Suppressor Proteins
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ATM protein, human
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Ataxia Telangiectasia Mutated Proteins
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Atm protein, mouse
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Protein Serine-Threonine Kinases