SHM1 (At4g37930, UniProt Q9SZJ5) - curation notes
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These notes are a manual literature summary built only from the cached
publications in publications/, the UniProt record (SHM1-uniprot.txt) and
PubMed searches. No -deep-research-*.md file exists for this gene.
Identity
- UniProt Q9SZJ5 (GLYM1_ARATH), "Serine hydroxymethyltransferase 1, mitochondrial";
gene SHM1, synonyms SHMT1 and STM (the historical stm/shm mutant); locus At4g37930.
- EC 2.1.2.1, RHEA:15481; PLP cofactor; SHMT family (PANTHER PTHR11680:SF61,
"SERINE HYDROXYMETHYLTRANSFERASE 1, MITOCHONDRIAL"); N-terminal transit peptide.
- Seven SHM genes in Arabidopsis; SHM1 and SHM2 are predicted to be mitochondrial
PMID:16339799.
Core function: photorespiratory glycine-to-serine conversion
- Mitochondrial SHMT, together with GDC, converts 2 glycine into CO2, NH4+ and
serine PMID:16339799.
- SHM uses the GDC-derived 5,10-methylene-THF to convert another glycine into serine
PMID:22303256.
- SHM1 is the photorespiratory isozyme, encoded by a single gene
PMID:22303256.
- Genetics: shm1-1 (the classical
stm) lacks mitochondrial SHMT activity and is
conditionally lethal in air; the defect maps to SHM1; SHM1 (35S or native
promoter) complements, SHM2 does not
PMID:16339799
PMID:16339799.
- SHM2 is excluded from mesophyll mitochondria, so it cannot replace SHM1 in
photorespiration; SHM1 and SHM2 act redundantly in one-carbon metabolism of
vascular cells; the shm1 shm2 double mutant is lethal even at high CO2
PMID:21976482
PMID:21976482.
Regulation and partners
- Fd-GOGAT (GLU1) is dual-targeted to mitochondria and physically interacts with
SHMT1; the interaction is needed for photorespiratory SHMT activity
PMID:19223513.
- UBP16 deubiquitinates and stabilizes SHM1; SHM1 is degraded by the 26S
proteasome PMID:23232097.
- FERONIA phosphorylates SHM1, affecting its stability, during salt stress
PMID:39197037.
- Ser31 phosphorylation mimic reduces SHMT1 protein and salt/drought tolerance
PMID:31134633.
- Circadian and light regulation of SHM1 mRNA
PMID:10806255
PMID:10806255.
- SHM transcript is overexpressed in the stm mutant, suggesting feedback regulation
(PMID:9232907).
Stress and defence phenotypes (indirect)
- shmt1-1 (weak allele, later called shm1-3): lesion formation, constitutive SA and
H2O2-detoxification gene expression, higher susceptibility to biotrophic and
necrotrophic pathogens, salt sensitivity
PMID:15659103
PMID:15659103.
These phenotypes are best explained by impaired photorespiratory flux causing ROS
accumulation, i.e. they are downstream consequences of the core enzymatic role.
- Photorespiratory mutants including SHMT-deficient lines show accelerated PSII
photoinhibition through impaired D1 repair (PMID:17400706).
Localization
- Mitochondrion: multiple proteomics and IDA (PMID:19223513, PMID:23232097),
predicted matrix targeting PMID:10806255.
- Cytosol (IDA, PMID:23232097; UniProt "Cytoplasm") might reflect a pre-import or
degradation pool, which fits proteasome-dependent turnover, but the full text is not
cached.
- Chloroplast stroma/thylakoid/stromule, nucleus, plasma membrane, apoplast and
cytosolic ribosome come from proteome datasets and are best treated as
contamination by an abundant leaf mitochondrial enzyme. The complex I study lists
"Ser hydroxymethyltransferase" among its contaminants (PMID:20197505), which
shows that SHMT carries over into other fractions.
Module cross-check
modules/photorespiration_c2_cycle.yaml step 6 (shmt_step) uses SHM1
(Q9SZJ5) with GO:0004372, process GO:0009853 and location GO:0005759.
This review agrees: core MF GO:0004372, photorespiration, mitochondrion /
mitochondrial matrix. No disagreement.