PXD048505-1
PXD048505 is an original dataset announced via ProteomeXchange.
Dataset Summary
Title | Mannose is crucial for mesoderm specification and symmetry breaking in gastruloids |
Description | Patterning and growth are fundamental features of embryonic development that must be tightly coordinated during morphogenesis. While metabolism is known to control cell growth, how it impacts patterning and links to morphogenesis is poorly understood. To understand how metabolism impacts early mesoderm specification during gastrulation, we used in vitro mouse embryonic stem (ES) cell-derived gastruloids, due to ease of metabolic manipulations and high-throughput nature. Gastruloids showed mosaic expression of glucose transporters co-expressing with the mesodermal marker T/Bra. To understand the significance of cellular glucose uptake in development, we used the glucose metabolism inhibitor 2-deoxy-D-glucose (2-DG). 2-DG blocked the expression of T/Bra and abolishes axial elongation in gastruloids. Surprisingly, removing glucose completely from the medium did not phenocopy 2-DG treatment despite a significant decline in glycolytic intermediates occurring under both conditions. As 2-DG can 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. We corroborated these results in vivomouse embryos where supplementing mannose rescued the 2-DG mediated phenotype of mesoderm specification and proximo-distal elongation of the primitive streak. We further showed that blocking production and intracellular recycling of mannose abrogated mesoderm specification. At molecular level, proteomics analysis revealed that mannose reversed glycosylation of the Wnt pathway regulator, Secreted Frizzled Receptor, Frzb, expressed in the primitive streak of the mouse embryo. Our study showed how mannose linked metabolism to glycosylation of a developmental pathway component, crucial in patterning of mesoderm and morphogenesis of gastruloids. |
HostingRepository | MassIVE |
AnnounceDate | 2024-03-12 |
AnnouncementXML | Submission_2024-03-12_01:37:44.047.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Adam Dowle |
SpeciesList | scientific name: Mus musculus; common name: house mouse; NCBI TaxID: 10090; |
ModificationList | Oxidation; Acetyl |
Instrument | timsTOF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
---|---|---|---|
0 | 2024-01-12 05:46:53 | ID requested | |
⏵ 1 | 2024-03-12 01:37:44 | announced |
Publication List
Chaitanya Dingare, Jenny Yang, Ben Steventon. Mannose is crucial for mesoderm specification and symmetry breaking in gastruloids. https://www.biorxiv.org/content/10.1101/2023.06.05.543730v2.full. |
Keyword List
submitter keyword: Gastruloids, Mesoderm, Mannose, N-glycosylation, Glycoprotein, Wnt |
Contact List
Benjamin Steventon | |
---|---|
contact affiliation | University of Cambridge |
contact email | bjs57@cam.ac.uk |
lab head | |
Adam Dowle | |
contact affiliation | University of York |
contact email | adam.dowle@york.ac.uk |
dataset submitter |
Full Dataset Link List
MassIVE dataset URI |
Dataset FTP location NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://massive.ucsd.edu/v06/MSV000093849/ |