PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of bmcmbBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Molecular Biology
 
BMC Mol Biol. 2012; 13: 27.
Published online Sep 7, 2012. doi:  10.1186/1471-2199-13-27
PMCID: PMC3482555
Clock-controlled mir-142-3p can target its activator, Bmal1
Xiaochao Tan,1 Peng Zhang,2 Lan Zhou,2 Bin Yin,1 Hui Pan,corresponding author3 and Xiaozhong Pengcorresponding author1
1State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China
2Department of Physiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China
3Department of Endocrinology, Peking Union Medical Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China
corresponding authorCorresponding author.
Xiaochao Tan: xiaochtan/at/yahoo.cn; Peng Zhang: je_800115/at/yahoo.com.cn; Lan Zhou: zhoulan2011/at/126.com; Bin Yin: yinbin_pumc/at/yahoo.com.cn; Hui Pan: ph3610/at/gmail.com; Xiaozhong Peng: pengxiaozhong/at/pumc.edu.cn
Received April 26, 2012; Accepted August 23, 2012.
Abstract
Background
microRNAs (miRNAs) are shown to be involved in the regulation of circadian clock. However, it remains largely unknown whether miRNAs can regulate the core clock genes (Clock and Bmal1).
Results
In this study, we found that mir-142-3p directly targeted the 3’UTR of human BMAL1 and mouse Bmal1. The over-expression (in 293ET and NIH3T3 cells) and knockdown (in U87MG cells) of mir-142-3p reduced and up-regulated the Bmal1/BMAL1 mRNA and protein levels, respectively. Moreover, the expression level of mir-142-3p oscillated in serum-shocked NIH3T3 cells and the results of ChIP and luciferase reporter assays suggested that the expression of mir-142-3p was directly controlled by CLOCK/BMAL1 heterodimers in NIH3T3 cells.
Conclusions
Our study demonstrates that mir-142-3p can directly target the 3’UTR of Bmal1. In addition, the expression of mir-142-3p is controlled by CLOCK/BMAL1 heterodimers, suggesting a potential negative feedback loop consisting of the miRNAs and the core clock genes. These findings open new perspective for studying the molecular mechanism of circadian clock.
Keywords: mir-142-3p, Bmal1, Circadian clock
Articles from BMC Molecular Biology are provided here courtesy of
BioMed Central