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   Identification of radiation-Induced MicroRNA transcriptome by next-Generation massively parallel sequencing  
   
نویسنده chaudhry m.a. ,omaruddin r.a. ,brumbaugh c.d. ,tariq m.a. ,pourmand n.
منبع journal of radiation research - 2013 - دوره : 54 - شماره : 5 - صفحه:808 -822
چکیده    Gene regulation in cells exposed to ionizing radiation (ir) occurs at the transcriptional and post-transcriptional levels. recent studies have suggested that micro-rna (mirna) play a significant role in post-transcriptional gene regulation in irradiated cells. mirna are rna molecules 18-24 nucleotides in length that are involved in negatively regulating the stability or translation of target messenger rna. previous studies from our laboratory have shown that the expression of various mirna is altered in ir-treated cells. in the present study we monitored genome-wide expression changes of mirna transcriptome by massively parallel sequencing of human cells irradiated with x-rays. the baseline expression of 402 mirna indicated a wide range of modulation without exposure to ir. differences in the expression of many mirna were observed in a timedependent fashion following radiation treatment. the short time-series expression miner (stem) clustering tool was used to characterize 190 mirna to six statistically significant temporal expression profiles. mir-19b and mir-93 were induced and mir-222,mir-92a,and mir-941 were repressed after radiation treatment. mir-142-3p,mir-142-5p,mir-107,mir-106b,mir-191,mir-21,mir-26a,mir-182,mir-16,mir-146a,mir-22 and mir-30e exhibited two peaks of induction: one at 8 h and the other at 24 h post-irradiation. mir-378,mir-let-7a,mir-let-7g,mir-let-7f,mir-103b,mir-486-3p,mir-423-5p,mir-4448,mir-3607-5p,mir-20b,mir-130b,mir-155,mir-181,mir-30d and mir-378c were induced only at the 8-h time-point. this catalogue of the inventory of mirna that are modulated as a response to radiation exposure will be useful for explaining the mechanisms of gene regulation under conditions of stress. © the author 2013. published by oxford university press on behalf of the japan radiation research society and japanese society for therapeutic radiology and oncology.
کلیدواژه Differential gene expression; Micro-RNA; Next-generation sequencing; Radiation effects; TK6 cells
آدرس department of medical laboratory and radiation sciences,university of vermont,burlington,vt 05405, United States, department of medical laboratory and radiation sciences,university of vermont,burlington,vt 05405, United States, department of biomolecular engineering,university of california at santa cruz,santa cruz,ca 95064, United States, department of biomolecular engineering,university of california at santa cruz,santa cruz,ca 95064, United States, department of biomolecular engineering,university of california at santa cruz,santa cruz,ca 95064, United States
 
     
   
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