Summary of Study ST003120

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 PR001938. The data can be accessed directly via it's Project DOI: 10.21228/M86T69 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

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.

Show all samples  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST003120
Study TitleMannose is crucial for mesoderm specification and symmetry breaking in gastruloids.
Study SummaryPatterning and growth are fundamental features of embryonic development that must be tightly coordinated. To understand how metabolism impacts early mesoderm development, we used mouse embryonic stem cell-derived gastruloids, that co-expressed glucose transporters with the mesodermal marker T/Bra. While the glucose mimic, 2-deoxy-D-glucose (2-DG), blocked T/Bra expression and abolished axial elongation in gastruloids, removal of glucose did not phenocopy 2-DG treatment despite a decline in glycolytic intermediates occurring under both conditions. As 2-DG could also act as a competitive inhibitor of mannose in protein glycosylation, we added mannose together with 2-DG and found that it could rescue the mesoderm specification both in vivo and in vitro. We further showed that blocking production and intracellular recycling of mannose abrogated mesoderm specification. Proteomics analysis revealed that mannose reversed glycosylation of the Wnt pathway regulator, Secreted Frizzled Receptor, Frzb. Our study showed how mannose is crucial for mesoderm specification in gastruloids.
Institute
Dept of Genetics, University of Cambridge
Last NameDingare
First NameChaitanya
AddressDowning Site, Cambridge, Cambridgeshire, CB2 3EH, United Kingdom
Emailcd705@cam.ac.uk
Phone+447916677460
Submit Date2024-02-24
Publicationshttps://doi.org/10.1101/2023.06.05.543730
Raw Data AvailableYes
Raw Data File Type(s)mzML, raw(Thermo)
Analysis Type DetailLC-MS
Release Date2024-03-13
Release Version1
Chaitanya Dingare Chaitanya Dingare
https://dx.doi.org/10.21228/M86T69
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Factors:

Subject type: Cultured cells; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Treatment
SA338087CD044_002Mouse Embryonic Stem Cells 1X Glucose
SA338088CD043_002Mouse Embryonic Stem Cells 1X Glucose
SA338089CD042_002Mouse Embryonic Stem Cells 1X Glucose
SA338090CD041_002Mouse Embryonic Stem Cells 1X Glucose
SA338091CD044_004Mouse Embryonic Stem Cells 2DG_5mM
SA338092CD042_004Mouse Embryonic Stem Cells 2DG_5mM
SA338093CD043_004Mouse Embryonic Stem Cells 2DG_5mM
SA338094CD041_004Mouse Embryonic Stem Cells 2DG_5mM
SA338095CD042_003Mouse Embryonic Stem Cells 3X Glucose
SA338096CD044_003Mouse Embryonic Stem Cells 3X Glucose
SA338097CD041_003Mouse Embryonic Stem Cells 3X Glucose
SA338098CD043_003Mouse Embryonic Stem Cells 3X Glucose
SA338099Proc_Blank_startMouse Embryonic Stem Cells Blank
SA338100CD043_001Mouse Embryonic Stem Cells No Glucose
SA338101CD042_001Mouse Embryonic Stem Cells No Glucose
SA338102CD044_001Mouse Embryonic Stem Cells No Glucose
SA338103CD041_001Mouse Embryonic Stem Cells No Glucose
SA338104QC12Mouse Embryonic Stem Cells Quality Control
SA338105QC10Mouse Embryonic Stem Cells Quality Control
SA338106QC08Mouse Embryonic Stem Cells Quality Control
SA338107QC09Mouse Embryonic Stem Cells Quality Control
SA338108QC11Mouse Embryonic Stem Cells Quality Control
Showing results 1 to 22 of 22
  logo