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Transcriptional Architecture and Chromatin Landscape of the Core Circadian Clock in Mammals
Open accessAbstract
Transcription Around the Clock: The biological clock that controls daily rhythms in mammalian physiology and behavior is thought to be regulated in large part by transcriptional events (see the Perspective by Doherty and Kay ). Koike et al. (p. 349 ; published online 30 August) produced a comprehensive analysis of these transcriptional events across the entire mouse liver genome over a 24-hour period. Only ∼22% of cycling messenger RNA transcripts were driven by de novo transcription, suggesting that posttranscriptional events also play an important regulatory role in the mammalian clock. Biological timing in organisms can also respond to rhythmic cues from the environment. Morf et al. (p. 379 , published online 23 August) explored how one such cue, cycles in ambient temperature, influence circadian timing in mammalian cells. Cold-inducible RNA–binding protein (CIRP) accumulates when body temperature is low. A systematic search for binding partners of CIRP identified RNA encoding core components of the circadian clock. Loss of CIRP decreased the amplitude of circadian gene expression and cells lacking CIRP adapted more quickly to temperature cycles.
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“In the livers of WT mice, BMAL1/CLOCK transcriptional activity is low at ZT2 and 18 but peaks at ZT6 (Koike et al., 2012)”
From Circadian Homeostasis of Liver Metabolism Suppresses Hepatocarcinogenesis (2016) · cites this paper as Koike et al., 2012
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Cites
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
Langmead, B., Trapnell, C., Pop, M., & Salzberg, S. L. (2009) · Genome Biology · doi:10.1186/gb-2009-10-3-r25 · Cited by 21,849
Model-based Analysis of ChIP-Seq (MACS)
Zhang, Y., Liu, T., Meyer, C. A., Eeckhoute, J., Johnson, D. S., Bernstein, B. E., Nusbaum, C., Myers, R. M., Brown, M., Li, W., et al. (2008) · Genome Biology · doi:10.1186/gb-2008-9-9-r137 · Cited by 18,386
Heinz, S., Benner, C., Spann, N., Bertolino, E., Lin, Y. C., Laslo, P., Cheng, J. X., Murre, C., Singh, H., & Glass, C. K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.004 · Cited by 13,382
TopHat: discovering splice junctions with RNA-Seq
Trapnell, C., Pachter, L. S., & Salzberg, S. L. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp120 · Cited by 11,682
The Human Genome Browser at UCSC
Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., & Haussler, A. D. (2002) · Genome Research · doi:10.1101/gr.229102 · Cited by 10,400
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
Histone H3K27ac separates active from poised enhancers and predicts developmental state
Creyghton, M. P., Cheng, A. W., Welstead, G. G., Kooistra, T., Carey, B. W., Steine, E. J., Hanna, J., Lodato, M. A., Frampton, G. M., Sharp, P. A., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016071107 · Cited by 4,302
The Role of Chromatin during Transcription
Li, B., Carey, M., & Workman, J. L. (2007) · Cell · doi:10.1016/j.cell.2007.01.015 · Cited by 3,503
Heintzman, N. D., Stuart, R. K., Hon, G., Fu, Y., Ching, C. W., Hawkins, R. D., Barrera, L. O., Van Calcar, S., Qu, C., Ching, K. A., et al. (2007) · Nature Genetics · doi:10.1038/ng1966 · Cited by 3,398
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Circadian transcription from beta cell function to diabetes pathophysiology
Perelis, M., Ramsey, K. M., Marcheva, B., & Bass, J. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416656949 · Cited by 57
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Wang, G.-Z., Hickey, S. L., Shi, L., Huang, H.-C., Nakashe, P., Koike, N., Tu, B. P., Takahashi, J. S., & Konopka, G. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.043 · Cited by 59
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Alternative splicing coupled mRNA decay shapes the temperature‐dependent transcriptome
Neumann, A., Meinke, S., Goldammer, G., Strauch, M., Schubert, D. S. P., Timmermann, B., Heyd, F., & Preußner, M. (2020) · EMBO Reports · doi:10.15252/embr.202051369 · Cited by 54
Boucher, H., Vanneaux, V., Domet, T., Parouchev, A., & Larghero, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146674 · Cited by 57
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Early, J. O., & Curtis, A. M. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.10.006 · Cited by 60
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Brown, M., Sen, S., Mazzone, A., Her, T. K., Xiong, Y., Lee, J., Javeed, N., Colwell, C. S., Rakshit, K., LeBrasseur, N. K., et al. (2021) · Science Advances · doi:10.1126/sciadv.abg6856 · Cited by 55
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Akashi, M., Okamoto, A., Tsuchiya, Y., Todo, T., Nishida, E., & Node, K. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.072 · Cited by 54
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Fan, Z., Zhao, M. L., Joshi, P. D., Li, P., Zhang, Y., Guo, W., Xu, Y., Wang, H., Zhao, Z., & Yan, J. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx156 · Cited by 50
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Self-citationKim, H. K., Lee, S. Y., Koike, N., Kim, E., Wirianto, M., Burish, M. J., Yagita, K., Lee, H. K., Chen, Z., Chung, J. M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-70757-w · Cited by 50
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Wu, G., Zhu, J., Yu, J. M., Zhou, L., Huang, J. Z., & Zhang, Z. (2014) · Journal of Biological Rhythms · doi:10.1177/0748730414537788 · Cited by 45
Zhou, Z., Liu, X., Hu, Q., Zhang, N., Sun, G., Cha, J., Wang, Y., Liu, Y., & He, Q. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315133110 · Cited by 46
Li, N., Joska, T. M., Ruesch, C. E., Coster, S. J., & Belden, W. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406130112 · Cited by 45
Jangani, M., Poolman, T. M., Matthews, L. C., Yang, N., Farrow, S. N., Berry, A. A., Hanley, N. A., Williamson, A. J. K., Whetton, A. D., Donn, R. P., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.540906 · Cited by 49
Ma, D., Liu, T., Chang, L., Rui, C., Xiao, Y., Li, S., Hogenesch, J. B., Chen, Y. E., & Lin, J. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.685982 · Cited by 44
McCarthy, M. J. (2018) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000215 · Cited by 49
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Pivonello, C., Negri, M., Patalano, R., Amatrudo, F., Montò, T., Liccardi, A., Graziadio, C., Muscogiuri, G., Pivonello, R., & Colao, A. (2021) · Obesity Reviews · doi:10.1111/obr.13390 · Cited by 49
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Yang, G., Paschos, G. K., Curtis, A. M., Musiek, E. S., McLoughlin, S. C., & FitzGerald, G. A. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3007225 · Cited by 45
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Green, C. B. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a030692 · Cited by 46
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Fame, R. M., Kalugin, P. N., Petrova, B., Xu, H., Soden, P. A., Shipley, F. B., Dani, N., Grant, B. F., Pragana, A., Head, J. P., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39326-3 · Cited by 43
Molecular mechanisms of artificial light at night affecting circadian rhythm disturbance
Lei, T., Hua, H., Du, H., Xia, J., Xu, D., Liu, W., Wang, Y., & Yang, T. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03647-5 · Cited by 48
m6A mRNA Methylation: A New Circadian Pacesetter
Hastings, M. H. (2013) · Cell · doi:10.1016/j.cell.2013.10.028 · Cited by 44
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Metadata
- Authors
- Koike, N., Yoo, S.-H., Huang, H.-C., Kumar, V., Lee, C., Kim, T.-K., & Takahashi, J. S.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Florida State University (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Takahashi, Joseph S.
- Venue
- Science
- Published
- 2012-10-19
- Volume
- 338
- Issue
- 6105
- Pages
- 349-354
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3694775
- OpenAlex
- W2091531174
- Cited by
- 1,464
- References
- 80
- Citations by year
- 2026: 72 · 2025: 99 · 2024: 93 · 2023: 97 · 2022: 121 · 2021: 112 · 2020: 158 · 2019: 105 · 2018: 109 · 2017: 97 · 2016: 111 · 2015: 102 · 2014: 102 · 2013: 72 · 2012: 13
- FWCI
- 41.23
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Open Access System for Information Sharing (Pohang University of Science and Technology) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute on Drug Abuse (F32DA024556)
- National Institute of Neurological Disorders and Stroke (R01NS053616)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- circadian clock, transcriptional feedback loop, clocks, Bmal1, period gene, RNA polymerase II recruitment, chromatin remodeling, transcription factor binding, de novo transcription, post-transcriptional regulation, mouse liver, chromatin state
- MeSH terms
- Animals, Chromatin, Enhancer Elements, Genetic, Histones, Liver, Male, Mice, Inbred C57BL, RNA Polymerase II, RNA, Messenger, Transcription, Genetic, Transcriptional Activation, Gene Expression Profiling, DNA, Intergenic, Chromatin Assembly and Disassembly, Epigenesis, Genetic, Mice, Genetic Loci, CLOCK Proteins, ARNTL Transcription Factors, Cryptochromes, Period Circadian Proteins, Circadian Clocks
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