生物
昼夜节律
生物钟
效应器
转录因子
基因调控网络
表观遗传学
遗传学
基因表达调控
基因
细胞生物学
基因敲除
转录调控
基因表达
转录组
细菌昼夜节律
调节器
计算生物学
神经科学
作者
Sandra Schick,Kolja Becker,Sudhir Thakurela,David Fournier,Mareike Hildegard Hampel,Stefan Legewie,Vijay Tiwari
摘要
Organisms adapt their physiology and behavior to the 24-h day-night cycle to which they are exposed. On a cellular level, this is regulated by intrinsic transcriptional-translational feedback loops that are important for maintaining the circadian rhythm. These loops are organized by members of the core clock network, which further regulate transcription of downstream genes, resulting in their circadian expression. Despite progress in understanding circadian gene expression, only a few players involved in circadian transcriptional regulation, including transcription factors, epigenetic regulators, and long noncoding RNAs, are known. Aiming to discover such genes, we performed a high-coverage transcriptome analysis of a circadian time course in murine fibroblast cells. In combination with a newly developed algorithm, we identified many transcription factors, epigenetic regulators, and long intergenic noncoding RNAs that are cyclically expressed. In addition, a number of these genes also showed circadian expression in mouse tissues. Furthermore, the knockdown of one such factor, Zfp28, influenced the core clock network. Mathematical modeling was able to predict putative regulator-effector interactions between the identified circadian genes and may help for investigations into the gene regulatory networks underlying circadian rhythms.
科研通智能强力驱动
Strongly Powered by AbleSci AI