Summary of Study ST002079

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001319. The data can be accessed directly via it's Project DOI: 10.21228/M87125 This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002079
Study TitleDefining the mammalian coactivation of hepatic 12-hour clock and lipid metabolism
Study SummaryThe 12-hour clock coordinates lipid homeostasis, energy metabolism and stress rhythms via the transcriptional regulator XBP1. However, the biochemical and physiological basis for integrated control of the 12-hour clock and diverse metabolic pathways remains unclear. Here, we show that steroid receptor coactivator SRC-3 coactivates XBP1 transcription and regulates hepatic 12-hour cistrome and gene rhythmicity. Mice lacking SRC-3 show abnormal 12-hour rhythms in hepatic transcription, metabolic functions, systemic energetics, and rate-limiting lipid metabolic processes including triglyceride, phospholipid and cardiolipin pathways. Notably, 12-hour clock coactivation is not only preserved, with its cistromic activation priming ahead of the zeitgeber cue of light, but concomitant with rhythmic remodeling in the absence of food. These findings reveal that SRC-3 integrates the mammalian 12-hour clock, energy metabolism, and membrane and lipid homeostasis, and demonstrates a role for the 12-hour clock machinery as an active transcriptional mechanism in anticipating physiological and metabolic energy needs and stresses.
Institute
Baylor College of Medicine
Last NameMeng
First NameHuan
AddressOne Baylor Plaza BCM 130 Houston, TX 77030
Emailhuanm@bcm.edu
Phone5127729532
Submit Date2022-02-04
Num Groups12
Total Subjects24
Num Males24
Raw Data AvailableYes
Raw Data File Type(s)wiff
Analysis Type DetailOther
Release Date2022-02-22
Release Version1
Huan Meng Huan Meng
https://dx.doi.org/10.21228/M87125
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN003391 AN003392
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Shimadzu CTO-20A Nexera X2 UHPLC systems Shimadzu CTO-20A Nexera X2 UHPLC systems
Column Waters Acquity BEH HSS T3 (50 x 2.1mm,1.8um) Waters Acquity BEH HSS T3 (50 x 2.1mm,1.8um)
MS Type ESI ESI
MS instrument type Triple TOF Triple TOF
MS instrument name ABI Sciex 5600+ TripleTOF ABI Sciex 5600+ TripleTOF
Ion Mode POSITIVE NEGATIVE
Units Normalized intensity Normalized intensity

MS:

MS ID:MS003158
Analysis ID:AN003391
Instrument Name:ABI Sciex 5600+ TripleTOF
Instrument Type:Triple TOF
MS Type:ESI
MS Comments:The data acquisition of each sample was performed in both positive and negative ionization modes using a TripleTOF 5600 equipped with a Turbo VTM ion source (AB Sciex, Concord, Canada).
Ion Mode:POSITIVE
  
MS ID:MS003159
Analysis ID:AN003392
Instrument Name:ABI Sciex 5600+ TripleTOF
Instrument Type:Triple TOF
MS Type:ESI
MS Comments:The data acquisition of each sample was performed in both positive and negative ionization modes using a TripleTOF 5600 equipped with a Turbo VTM ion source (AB Sciex, Concord, Canada).
Ion Mode:NEGATIVE
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