TY - JOUR
T1 - Circadian rhythms in the tissue-specificity from metabolism to immunity
T2 - insights from omics studies
AU - Kinouchi, Kenichiro
AU - Mikami, Yohei
AU - Kanai, Takanori
AU - Itoh, Hiroshi
N1 - Funding Information:
This study was funded by Japan Society for the Promotion of Science ( JSPS ) KAKENHI (C) 19K09012 for KK, (B) 20H03666 for YM, and (A) 20H00536 for TK; Advanced Research and Development Programs for Medical Innovation (AMED-CREST ; 16gm1010003h0001 for TK and 20gm1210001h0002 for YM, Practical Research Project for Rare/Intractable Diseases; 21ek0109556h0001 for YM); Takeda Science Foundation; Kanae Foundation for The Promotion of Medical Science; Mishima Kaiun Memorial Foundation Resaerch Grant; Yakult Bio-Science Foundation; The NOVARTIS Foundation (Japan) for the Promotion of Science; The Japan Diabetes Society; Yamaguchi Endocrine Research Foundation; Mochida Memorial Foundation for Medical and Pharmaceutical Research; The Sumitomo Foundation; Keio University Medical Fund.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/8
Y1 - 2021/8
N2 - Creatures on earth have the capacity to preserve homeostasis in response to changing environments. The circadian clock enables organisms to adapt to daily predictable rhythms in surrounding conditions. In mammals, circadian clocks constitute hierarchical network, where the central pacemaker in hypothalamic suprachiasmatic nucleus (SCN) serves as a time-keeping machinery and governs peripheral clocks in every other organ through descending neural and humoral factors. The central clock in SCN is reset by light, whilst peripheral clocks are entrained by feeding-fasting rhythms, emphasizing the point that temporal patterns of nutrient availability specifies peripheral clock functions. Indeed, emerging evidence revealed various types of diets or timing of food intake reprogram circadian rhythms in a tissue specific manner. This advancement in understanding of mechanisms underlying tissue specific responsiveness of circadian oscillators to nutrients at the genomic and epigenomic levels is largely owing to employment of state-of-the-art technologies. Specifically, high-throughput transcriptome, proteome, and metabolome have provided insights into how genes, proteins, and metabolites behave over circadian cycles in a given tissue under a certain dietary condition in an unbiased fashion. Additionally, combinations with specialized types of sequencing such as nascent-seq and ribosomal profiling allow us to dissect how circadian rhythms are generated or obliterated at each step of gene regulation. Importantly, chromatin immunoprecipitation followed by deep sequencing methods provide chromatin landscape in terms of regulatory mechanisms of circadian gene expression. In this review, we outline recent discoveries on temporal genomic and epigenomic regulation of circadian rhythms, discussing entrainment of the circadian rhythms by feeding as a fundamental new comprehension of metabolism and immune response, and as a potential therapeutic strategy of metabolic and inflammatory diseases.
AB - Creatures on earth have the capacity to preserve homeostasis in response to changing environments. The circadian clock enables organisms to adapt to daily predictable rhythms in surrounding conditions. In mammals, circadian clocks constitute hierarchical network, where the central pacemaker in hypothalamic suprachiasmatic nucleus (SCN) serves as a time-keeping machinery and governs peripheral clocks in every other organ through descending neural and humoral factors. The central clock in SCN is reset by light, whilst peripheral clocks are entrained by feeding-fasting rhythms, emphasizing the point that temporal patterns of nutrient availability specifies peripheral clock functions. Indeed, emerging evidence revealed various types of diets or timing of food intake reprogram circadian rhythms in a tissue specific manner. This advancement in understanding of mechanisms underlying tissue specific responsiveness of circadian oscillators to nutrients at the genomic and epigenomic levels is largely owing to employment of state-of-the-art technologies. Specifically, high-throughput transcriptome, proteome, and metabolome have provided insights into how genes, proteins, and metabolites behave over circadian cycles in a given tissue under a certain dietary condition in an unbiased fashion. Additionally, combinations with specialized types of sequencing such as nascent-seq and ribosomal profiling allow us to dissect how circadian rhythms are generated or obliterated at each step of gene regulation. Importantly, chromatin immunoprecipitation followed by deep sequencing methods provide chromatin landscape in terms of regulatory mechanisms of circadian gene expression. In this review, we outline recent discoveries on temporal genomic and epigenomic regulation of circadian rhythms, discussing entrainment of the circadian rhythms by feeding as a fundamental new comprehension of metabolism and immune response, and as a potential therapeutic strategy of metabolic and inflammatory diseases.
KW - Bmal1
KW - Circadian clock
KW - Circadian rhythm
KW - Epigenetics
KW - Immunity
KW - Innate lymphoid cells
KW - Metabolism
UR - http://www.scopus.com/inward/record.url?scp=85108272188&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85108272188&partnerID=8YFLogxK
U2 - 10.1016/j.mam.2021.100984
DO - 10.1016/j.mam.2021.100984
M3 - Article
C2 - 34158177
AN - SCOPUS:85108272188
SN - 0098-2997
VL - 80
JO - Molecular Aspects of Medicine
JF - Molecular Aspects of Medicine
M1 - 100984
ER -