Global daily dynamics of the pineal transcriptome

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Standard

Global daily dynamics of the pineal transcriptome. / Bustos, Diego M; Bailey, Michael J; Sugden, David; Carter, David A; Rath, Martin F; Møller, Morten; Coon, Steven L; Weller, Joan L; Klein, David C.

I: Cell and Tissue Research, Bind 344, Nr. 1, 01.04.2011, s. 1-11.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bustos, DM, Bailey, MJ, Sugden, D, Carter, DA, Rath, MF, Møller, M, Coon, SL, Weller, JL & Klein, DC 2011, 'Global daily dynamics of the pineal transcriptome', Cell and Tissue Research, bind 344, nr. 1, s. 1-11. https://doi.org/10.1007/s00441-010-1094-1

APA

Bustos, D. M., Bailey, M. J., Sugden, D., Carter, D. A., Rath, M. F., Møller, M., Coon, S. L., Weller, J. L., & Klein, D. C. (2011). Global daily dynamics of the pineal transcriptome. Cell and Tissue Research, 344(1), 1-11. https://doi.org/10.1007/s00441-010-1094-1

Vancouver

Bustos DM, Bailey MJ, Sugden D, Carter DA, Rath MF, Møller M o.a. Global daily dynamics of the pineal transcriptome. Cell and Tissue Research. 2011 apr. 1;344(1):1-11. https://doi.org/10.1007/s00441-010-1094-1

Author

Bustos, Diego M ; Bailey, Michael J ; Sugden, David ; Carter, David A ; Rath, Martin F ; Møller, Morten ; Coon, Steven L ; Weller, Joan L ; Klein, David C. / Global daily dynamics of the pineal transcriptome. I: Cell and Tissue Research. 2011 ; Bind 344, Nr. 1. s. 1-11.

Bibtex

@article{b7677a4d12504e4fb122900265787146,
title = "Global daily dynamics of the pineal transcriptome",
abstract = "Transcriptome profiling of the pineal gland has revealed night/day differences in the expression of a major fraction of the genes active in this tissue, with two-thirds of these being nocturnal increases. A set of over 600 transcripts exhibit two-fold to >100-fold daily differences in abundance. These changes appear to be primarily attributable to adrenergic-cyclic-AMP-dependent mechanisms, which are controlled via a neural pathway that includes the suprachiasmatic nucleus, the master circadian oscillator. In addition to melatonin synthesis, night/day differences in gene expression impact genes associated with several specialized functions, including the immune/inflammation response, photo-transduction, and thyroid hormone/retinoic acid biology. The following nonspecialized cellular features are also affected: adhesion, cell cycle/cell death, cytoskeleton, DNA modification, endothelium, growth, RNA modification, small molecule biology, transcription factors, vesicle biology, signaling involving Ca(2+), cyclic nucleotides, phospholipids, mitogen-activated protein kinases, the Wnt signaling pathway, and protein phosphorylation.",
keywords = "Animals, Circadian Rhythm, Gene Expression Profiling, Gene Expression Regulation, Humans, Pineal Gland, Neurobiology. gene ekspression",
author = "Bustos, {Diego M} and Bailey, {Michael J} and David Sugden and Carter, {David A} and Rath, {Martin F} and Morten M{\o}ller and Coon, {Steven L} and Weller, {Joan L} and Klein, {David C}",
year = "2011",
month = apr,
day = "1",
doi = "10.1007/s00441-010-1094-1",
language = "English",
volume = "344",
pages = "1--11",
journal = "Cell and Tissue Research",
issn = "0302-766X",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - Global daily dynamics of the pineal transcriptome

AU - Bustos, Diego M

AU - Bailey, Michael J

AU - Sugden, David

AU - Carter, David A

AU - Rath, Martin F

AU - Møller, Morten

AU - Coon, Steven L

AU - Weller, Joan L

AU - Klein, David C

PY - 2011/4/1

Y1 - 2011/4/1

N2 - Transcriptome profiling of the pineal gland has revealed night/day differences in the expression of a major fraction of the genes active in this tissue, with two-thirds of these being nocturnal increases. A set of over 600 transcripts exhibit two-fold to >100-fold daily differences in abundance. These changes appear to be primarily attributable to adrenergic-cyclic-AMP-dependent mechanisms, which are controlled via a neural pathway that includes the suprachiasmatic nucleus, the master circadian oscillator. In addition to melatonin synthesis, night/day differences in gene expression impact genes associated with several specialized functions, including the immune/inflammation response, photo-transduction, and thyroid hormone/retinoic acid biology. The following nonspecialized cellular features are also affected: adhesion, cell cycle/cell death, cytoskeleton, DNA modification, endothelium, growth, RNA modification, small molecule biology, transcription factors, vesicle biology, signaling involving Ca(2+), cyclic nucleotides, phospholipids, mitogen-activated protein kinases, the Wnt signaling pathway, and protein phosphorylation.

AB - Transcriptome profiling of the pineal gland has revealed night/day differences in the expression of a major fraction of the genes active in this tissue, with two-thirds of these being nocturnal increases. A set of over 600 transcripts exhibit two-fold to >100-fold daily differences in abundance. These changes appear to be primarily attributable to adrenergic-cyclic-AMP-dependent mechanisms, which are controlled via a neural pathway that includes the suprachiasmatic nucleus, the master circadian oscillator. In addition to melatonin synthesis, night/day differences in gene expression impact genes associated with several specialized functions, including the immune/inflammation response, photo-transduction, and thyroid hormone/retinoic acid biology. The following nonspecialized cellular features are also affected: adhesion, cell cycle/cell death, cytoskeleton, DNA modification, endothelium, growth, RNA modification, small molecule biology, transcription factors, vesicle biology, signaling involving Ca(2+), cyclic nucleotides, phospholipids, mitogen-activated protein kinases, the Wnt signaling pathway, and protein phosphorylation.

KW - Animals

KW - Circadian Rhythm

KW - Gene Expression Profiling

KW - Gene Expression Regulation

KW - Humans

KW - Pineal Gland

KW - Neurobiology. gene ekspression

U2 - 10.1007/s00441-010-1094-1

DO - 10.1007/s00441-010-1094-1

M3 - Journal article

C2 - 21302120

VL - 344

SP - 1

EP - 11

JO - Cell and Tissue Research

JF - Cell and Tissue Research

SN - 0302-766X

IS - 1

ER -

ID: 33855090