4.8 Article

Microbiota Diumal Rhythmicity Programs Host Transcriptome Oscillations

期刊

CELL
卷 167, 期 6, 页码 1495-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2016.11.003

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资金

  1. Boehringer Ingelheim Fonds PhD Fellowship
  2. Ministry of Science, Technology Space, Israel
  3. Gilead Sciences International Research Scholars Program in Liver Disease
  4. CREST, Japan Agency for Medical Research and Development
  5. Crown Human Genome Center
  6. Else Kroener Fresenius Foundation
  7. European Research Council
  8. Israel Science Foundation
  9. Leona M. and Harry B. Helmsley Charitable Trust
  10. Gurwin Family Fund for Scientific Research
  11. Crown Endowment Fund for Immunological Research
  12. estate of Jack Gitlitz
  13. estate of Lydia Hershkovich
  14. Benoziyo Endowment Fund for the Advancement of Science
  15. Adelis Foundation
  16. CNRS (Centre National de la Recherche Scientifique)
  17. estate of Samuel and Alwyn J. Weber
  18. German-Israel Binational Foundation
  19. Minerva Foundation
  20. Rising Tide Foundation
  21. Alon Foundation scholar award

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The intestinal microbiota undergoes diurnal compositional and functional oscillations that affect metabolic homeostasis, but the mechanisms by which the rhythmic microbiota influences host circadian activity remain elusive. Using integrated multi-omics and imaging approaches, we demonstrate that the gut microbiota features oscillating biogeographical localization and metabolome patterns that determine the rhythmic exposure of the intestinal epithelium to different bacterial species and their metabolites over the course of a day. This diurnal microbial behavior drives, in turn, the global programming of the host circadian transcriptional, epigenetic, and metabolite oscillations. Surprisingly, disruption of homeostatic microbiome rhythmicity not only abrogates normal chromatin and transcriptional oscillations of the host, but also incites genome-wide de novo oscillations in both intestine and liver, thereby impacting diurnal fluctuations of host physiology and disease susceptibility. As such, the rhythmic biogeography and metabolome of the intestinal microbiota regulates the temporal organization and functional outcome of host transcriptional and epigenetic programs.

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