The 5-formyl-tetrahydrofolate proteome links folates with C/N metabolism and reveals feedback regulation of folate biosynthesis. Issue 10 (5th August 2021)
- Record Type:
- Journal Article
- Title:
- The 5-formyl-tetrahydrofolate proteome links folates with C/N metabolism and reveals feedback regulation of folate biosynthesis. Issue 10 (5th August 2021)
- Main Title:
- The 5-formyl-tetrahydrofolate proteome links folates with C/N metabolism and reveals feedback regulation of folate biosynthesis
- Authors:
- Li, Weichao
Liang, Qiuju
Mishra, Ratnesh Chandra
Sanchez-Mu�oz, Raul
Wang, Huan
Chen, Xin
Van Der Straeten, Dominique
Zhang, Chunyi
Xiao, Youli - Abstract:
- Abstract: Folates are indispensable for plant development, but their molecular mode of action remains elusive. We synthesized a probe, "5-F-THF-Dayne, " comprising 5-formyl-tetrahydrofolate (THF) coupled to a photoaffinity tag. Exploiting this probe in an affinity proteomics study in Arabidopsis thaliana, we retrieved 51 hits. Thirty interactions were independently validated with in vitro expressed proteins to bind 5-F-THF with high or low affinity. Interestingly, the interactors reveal associations beyond one-carbon metabolism, covering also connections to nitrogen (N) metabolism, carbohydrate metabolism/photosynthesis, and proteostasis. Two of the interactions, one with the folate biosynthetic enzyme DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE 1 ( At DHFR-TS1) and another with N metabolism-associated glutamine synthetase 1;4 ( At GLN1;4), were further characterized. In silico and experimental analyses revealed G35/K36 and E330 as key residues for the binding of 5-F-THF in At DHFR-TS1 and At GLN1;4, respectively. Site-directed mutagenesis of At GLN1;4 E330, which co-localizes with the ATP-binding pocket, abolished 5-F-THF binding as well as At GLN1;4 activity. Furthermore, 5-F-THF was noted to competitively inhibit the activities of At DHFR-TS1 and At GLN1;4. In summary, we demonstrated a regulatory role for 5-F-THF in N metabolism, revealed 5-F-THF-mediated feedback regulation of folate biosynthesis, and identified a total of 14 previously unknown high-affinity bindingAbstract: Folates are indispensable for plant development, but their molecular mode of action remains elusive. We synthesized a probe, "5-F-THF-Dayne, " comprising 5-formyl-tetrahydrofolate (THF) coupled to a photoaffinity tag. Exploiting this probe in an affinity proteomics study in Arabidopsis thaliana, we retrieved 51 hits. Thirty interactions were independently validated with in vitro expressed proteins to bind 5-F-THF with high or low affinity. Interestingly, the interactors reveal associations beyond one-carbon metabolism, covering also connections to nitrogen (N) metabolism, carbohydrate metabolism/photosynthesis, and proteostasis. Two of the interactions, one with the folate biosynthetic enzyme DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE 1 ( At DHFR-TS1) and another with N metabolism-associated glutamine synthetase 1;4 ( At GLN1;4), were further characterized. In silico and experimental analyses revealed G35/K36 and E330 as key residues for the binding of 5-F-THF in At DHFR-TS1 and At GLN1;4, respectively. Site-directed mutagenesis of At GLN1;4 E330, which co-localizes with the ATP-binding pocket, abolished 5-F-THF binding as well as At GLN1;4 activity. Furthermore, 5-F-THF was noted to competitively inhibit the activities of At DHFR-TS1 and At GLN1;4. In summary, we demonstrated a regulatory role for 5-F-THF in N metabolism, revealed 5-F-THF-mediated feedback regulation of folate biosynthesis, and identified a total of 14 previously unknown high-affinity binding cellular targets of 5-F-THF. Together, this sets a landmark toward understanding the role of folates in plant development. Abstract : Exploration of proteins that interact or bind with folates reveals folate-modulated growth and development in Arabidopsis. … (more)
- Is Part Of:
- The Plant Cell. Volume 33:Issue 10(2021)
- Journal:
- The Plant Cell
- Issue:
- Volume 33:Issue 10(2021)
- Issue Display:
- Volume 33, Issue 10 (2021)
- Year:
- 2021
- Volume:
- 33
- Issue:
- 10
- Issue Sort Value:
- 2021-0033-0010-0000
- Page Start:
- 3367
- Page End:
- 3385
- Publication Date:
- 2021-08-05
- Journal URLs:
- http://www.oxfordjournals.org/ ↗
- DOI:
- 10.1093/plcell/koab198 ↗
- Languages:
- English
- ISSNs:
- 1040-4651
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25617.xml