bioRxiv Science⌕ Search

Biology subjects

Bauwe, H.

Publications and source records attributed to Bauwe, H..

2 recordsLinked to original sources

GCS-H2 is essential for growth as it acts as the main relay for mitochondrial lipoylation in heterotrophic tissues of Arabidopsis thaliana

H-protein is part of the multi-protein glycine cleavage system found in both prokaryotes and eukaryotes. The Arabidopsis thaliana genome contains three loci for genes encoding H-protein. We show that in land plants, there are two clades of mitochondrial H-proteins; one that clusters with H1 and H3, and another that clusters with H2, an isoform mostly expressed in heterotrophic tissue and for which a null mutation results in a >99% impeded growth. After showing that all three isoforms fulfill the same metabolic function, we evidenced that the impaired root growth in h2 results from an altered cell cycle progression concomitant to a lower Target Of Rapamycin kinase activity. Subsequent metabolomic approaches revealed an accumulation of storage sugars and a significant decrease of the TCA intermediates and several vitamins in the h2 root cells as compared to the wild-type ones. Additional investigations evidenced that H2 acts as the main relay for lipoylation in root mitochondria, which diverges from the current lipoylation model proposed for photosynthetic tissues. Together, this work provides new insight on the control of the cell cycle by mitochondrial metabolism, and also challenges the current dogma for lipoylation in mitochondria of plant cells. Once sentence summaryThe absence of GCS-H2, an isoform of H-protein found in heterotrophic tissue, impedes the cell cycle, and drastically affects plant growth as it acts as the main relay for mitochondrial lipoylation.

plant biology↗

Stoichiometry of two plant glycine decarboxylase complexes and comparison with a cyanobacterial glycine cleavage system

The multienzyme glycine cleavage system (GCS) converts glycine and tetrahydrofolate to the one-carbon compound 5,10-methylenetetrahydrofolate, which is of vital importance for most if not all organisms. Photorespiring plant mitochondria contain very high levels of GCS proteins organised as a fragile glycine decarboxylase complex (GDC). The aim of this study is to provide mass spectrometry-based stoichiometric data for the plant leaf GDC and examine whether complex formation could be a general property of the GCS in photosynthesizing organisms. The molar ratios of the leaf GDC component proteins are 1L2-4P2-8T-26H and 1L2-4P2-8T-20H for pea and Arabidopsis, respectively, as determined by mass spectrometry. The minimum mass of the plant leaf GDC ranges from 1,550-1,650 kDa, which is larger than previously assumed. The Arabidopsis GDC contains four times more of the isoforms GCS-P1 and GCS-L1 in comparison with GCS-P2 and GCS-L2, respectively, whereas the H-isoproteins GCS-H1 and GCS-H3 are fully redundant as indicated by their about equal amounts. Isoform GCS-H2 is not present in leaf mitochondria. In the cyanobacterium Synechocystis sp. PCC 6803, GCS proteins are present at low concentration but above the complex formation threshold reported for pea leaf GDC. Indeed, formation of a cyanobacterial GDC from the individual recombinant GCS proteins in vitro could be demonstrated. Presence and metabolic significance of a Synechocystis GDC in vivo remain to be examined but could involve multimers of the GCS H-protein that dynamically crosslink the three GCS enzyme proteins, facilitating glycine metabolism by the formation of multienzyme metabolic complexes.

plant biology↗