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Changes in MicroRNA expression patterns in human fibroblasts after low‐LET radiation
Author(s) -
Maes Olivier C.,
An Jin,
Sarojini Harshini,
Wu Honglu,
Wang Eugenia
Publication year - 2008
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21878
Subject(s) - microrna , biology , dna damage , gene expression , apoptosis , dna repair , microbiology and biotechnology , cell cycle , gene , regulation of gene expression , gene expression profiling , genetics , dna
Exposure to radiation provokes cellular responses controlled in part by gene expression networks. MicroRNAs (miRNAs) are small non‐coding RNAs which mostly regulate gene expression by degrading the messages or inhibiting translation. Here, we investigated changes in miRNA expression patterns after low (0.1 Gy) and high (2.0 Gy) doses of X‐ray in human fibroblasts. At early (0.5 h) and late (6 and 24 h) time points, irradiation caused qualitative and quantitative differences in the down‐regulation of miRNA levels, including miR‐92b, 137, 660, and 656. A transient up‐regulation of miRNAs was observed after 2 h post‐irradiation following high doses of radiation, including miR‐558 and 662. MicroRNA levels were inversely correlated with targets from mRNA and proteomic profiling after 2.0 Gy of radiation. MicroRNAs miR‐579, 608, 548‐3p, and 585 are noted for targeting genes involved in radioresponsive mechanisms, such as cell cycle checkpoint and apoptosis. We suggest here a model in which miRNAs may act as “hub” regulators of specific cellular responses, immediately down‐regulated so as to stimulate DNA repair mechanisms, followed by up‐regulation involved in suppressing apoptosis for cell survival. Taken together, miRNAs may mediate signaling pathways in sequential fashion in response to radiation, and may serve as biodosimetric markers of radiation exposure. J. Cell. Biochem. 105: 824–834, 2008. © 2008 Wiley‐Liss, Inc.