MassIVE MSV000080766

Imported Reanalysis Dataset Public PXD001085

PHD3 and FIH substrates cluster in distinct signalling pathways

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Description

Amino acid hydroxylation is a common post-translational modification which regulates intra and inter-molecular protein-protein interactions. The modifications are regulated by a family of 2-oxoglutarate (2OG) dependent enzymes and although the biochemistry is well understood, until now only a few substrates have been described for these enzymes. We present here a sensitive method which specifically enriches and identifies hydroxylase substrates. We screened for substrates of PHD3 and FIH, a proline and asparagine hydroxylase respectively which regulate the HIF-mediated hypoxic response and were able to confirm known substrates as well as identifying hundreds of potential novel ones. Enrichment analysis revealed that the substrates of both hydroxylases cluster in the same pathways but frequently modify different nodes of these networks. We confirm that two proteins identified in this screen, MAPK6 and RIPK4, are indeed hydroxylated in a FIH or PHD3 dependent mechanism and explore the biological consequences of the hydroxylation. [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Hypoxia ; Hydroxylases ; DMOG ; RIPK4 ; ERK3 ; MAPK6

Contact

Principal Investigators:
(in alphabetical order) 		Alex von Kriegsheim, systems biology Ireland, UCD, N/A
Submitting User: ccms

Publications

Rodriguez J, Pilkington R, Garcia Munoz A, Nguyen LK, Rauch N, Kennedy S, Monsefi N, Herrero A, Taylor CT, von Kriegsheim A.
Substrate-Trapped Interactors of PHD3 and FIH Cluster in Distinct Signaling Pathways.
Cell Rep. 2016 Mar 22;14(11):2745-60. Epub 2016 Mar 10.

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