Predicted MicroRNAs for Mammalian Circadian Rhythms

被引:20
|
作者
Figueredo, Diego de Siqueira [1 ]
Barbosa, Mayara Rodrigues [1 ]
Goes Gitai, Daniel Leite [2 ]
de Andrade, Tiago Gomes [1 ]
机构
[1] Univ Fed Alagoas, Lab Mol Biol & Gene Express Anal, Campus Arapiraca, Alagoas, Brazil
[2] Univ Fed Alagoas, Lab Cellular & Mol Biol, Maceio, Alagoas, Brazil
关键词
posttranscriptional regulation; miR; bioinformatics; mammals; clock genes; CLOCK GENE-EXPRESSION; PPAR-GAMMA; ADIPOCYTE DIFFERENTIATION; TRANSCRIPTION FACTOR; MONONUCLEAR; LEUKOCYTES; MIRNA; IDENTIFICATION; ADIPOGENESIS; CONTRIBUTES;
D O I
10.1177/0748730413476827
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is little evidence for the involvement of microRNAs (miRs) in the regulation of circadian rhythms, despite the potential relevance of these elements in the posttranscriptional regulation of the clock machinery. The present work aimed to identify miRs targeting circadian genes through a predictive analysis of conserved miRs in mammals. Besides 23 miRs previously associated with circadian rhythms, we found a number of interesting candidate genes, equally predicted by the 3 software programs used, including miR-9, miR-24, miR25, miR-26, miR-27, miR-29, miR-93, miR-211, miR-302, and miR-346. Moreover, several miRs are predicted to be regulated by circadian transcription factors, such as CLOCK/BMAL, DEC2, and REV-ERBalpha. Using real-time PCR we demonstrated that the selected candidate miR-27b showed a daily variation in human leukocytes. This study presents predicted feedback loops for mammalian molecular clock and the first description of an miR with in vivo daily variation in humans.
引用
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页码:107 / 116
页数:10
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