Cargando…

Harmonics of Circadian Gene Transcription in Mammals

The circadian clock is a molecular and cellular oscillator found in most mammalian tissues that regulates rhythmic physiology and behavior. Numerous investigations have addressed the contribution of circadian rhythmicity to cellular, organ, and organismal physiology. We recently developed a method t...

Descripción completa

Detalles Bibliográficos
Autores principales: Hughes, Michael E., DiTacchio, Luciano, Hayes, Kevin R., Vollmers, Christopher, Pulivarthy, S., Baggs, Julie E., Panda, Satchidananda, Hogenesch, John B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654964/
https://www.ncbi.nlm.nih.gov/pubmed/19343201
http://dx.doi.org/10.1371/journal.pgen.1000442
_version_ 1782165425365188608
author Hughes, Michael E.
DiTacchio, Luciano
Hayes, Kevin R.
Vollmers, Christopher
Pulivarthy, S.
Baggs, Julie E.
Panda, Satchidananda
Hogenesch, John B.
author_facet Hughes, Michael E.
DiTacchio, Luciano
Hayes, Kevin R.
Vollmers, Christopher
Pulivarthy, S.
Baggs, Julie E.
Panda, Satchidananda
Hogenesch, John B.
author_sort Hughes, Michael E.
collection PubMed
description The circadian clock is a molecular and cellular oscillator found in most mammalian tissues that regulates rhythmic physiology and behavior. Numerous investigations have addressed the contribution of circadian rhythmicity to cellular, organ, and organismal physiology. We recently developed a method to look at transcriptional oscillations with unprecedented precision and accuracy using high-density time sampling. Here, we report a comparison of oscillating transcription from mouse liver, NIH3T3, and U2OS cells. Several surprising observations resulted from this study, including a 100-fold difference in the number of cycling transcripts in autonomous cellular models of the oscillator versus tissues harvested from intact mice. Strikingly, we found two clusters of genes that cycle at the second and third harmonic of circadian rhythmicity in liver, but not cultured cells. Validation experiments show that 12-hour oscillatory transcripts occur in several other peripheral tissues as well including heart, kidney, and lungs. These harmonics are lost ex vivo, as well as under restricted feeding conditions. Taken in sum, these studies illustrate the importance of time sampling with respect to multiple testing, suggest caution in use of autonomous cellular models to study clock output, and demonstrate the existence of harmonics of circadian gene expression in the mouse.
format Text
id pubmed-2654964
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26549642009-04-03 Harmonics of Circadian Gene Transcription in Mammals Hughes, Michael E. DiTacchio, Luciano Hayes, Kevin R. Vollmers, Christopher Pulivarthy, S. Baggs, Julie E. Panda, Satchidananda Hogenesch, John B. PLoS Genet Research Article The circadian clock is a molecular and cellular oscillator found in most mammalian tissues that regulates rhythmic physiology and behavior. Numerous investigations have addressed the contribution of circadian rhythmicity to cellular, organ, and organismal physiology. We recently developed a method to look at transcriptional oscillations with unprecedented precision and accuracy using high-density time sampling. Here, we report a comparison of oscillating transcription from mouse liver, NIH3T3, and U2OS cells. Several surprising observations resulted from this study, including a 100-fold difference in the number of cycling transcripts in autonomous cellular models of the oscillator versus tissues harvested from intact mice. Strikingly, we found two clusters of genes that cycle at the second and third harmonic of circadian rhythmicity in liver, but not cultured cells. Validation experiments show that 12-hour oscillatory transcripts occur in several other peripheral tissues as well including heart, kidney, and lungs. These harmonics are lost ex vivo, as well as under restricted feeding conditions. Taken in sum, these studies illustrate the importance of time sampling with respect to multiple testing, suggest caution in use of autonomous cellular models to study clock output, and demonstrate the existence of harmonics of circadian gene expression in the mouse. Public Library of Science 2009-04-03 /pmc/articles/PMC2654964/ /pubmed/19343201 http://dx.doi.org/10.1371/journal.pgen.1000442 Text en Hughes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hughes, Michael E.
DiTacchio, Luciano
Hayes, Kevin R.
Vollmers, Christopher
Pulivarthy, S.
Baggs, Julie E.
Panda, Satchidananda
Hogenesch, John B.
Harmonics of Circadian Gene Transcription in Mammals
title Harmonics of Circadian Gene Transcription in Mammals
title_full Harmonics of Circadian Gene Transcription in Mammals
title_fullStr Harmonics of Circadian Gene Transcription in Mammals
title_full_unstemmed Harmonics of Circadian Gene Transcription in Mammals
title_short Harmonics of Circadian Gene Transcription in Mammals
title_sort harmonics of circadian gene transcription in mammals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654964/
https://www.ncbi.nlm.nih.gov/pubmed/19343201
http://dx.doi.org/10.1371/journal.pgen.1000442
work_keys_str_mv AT hughesmichaele harmonicsofcircadiangenetranscriptioninmammals
AT ditacchioluciano harmonicsofcircadiangenetranscriptioninmammals
AT hayeskevinr harmonicsofcircadiangenetranscriptioninmammals
AT vollmerschristopher harmonicsofcircadiangenetranscriptioninmammals
AT pulivarthys harmonicsofcircadiangenetranscriptioninmammals
AT baggsjuliee harmonicsofcircadiangenetranscriptioninmammals
AT pandasatchidananda harmonicsofcircadiangenetranscriptioninmammals
AT hogeneschjohnb harmonicsofcircadiangenetranscriptioninmammals