Dietary-derived vitamin B12 protects Caenorhabditis elegans from thiol-reducing agents.
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
/ genetics
Animals
Caenorhabditis elegans
/ metabolism
Carbon
/ metabolism
Dithiothreitol
/ metabolism
Folic Acid
/ metabolism
Homocysteine
/ metabolism
Hydrogen Sulfide
/ metabolism
Ligases
/ metabolism
Lipids
Mercaptoethanol
/ metabolism
Methionine
/ metabolism
Methyltransferases
/ genetics
Nucleic Acids
Oxygen
/ metabolism
Reducing Agents
/ metabolism
S-Adenosylmethionine
/ metabolism
Sulfhydryl Compounds
/ metabolism
Vitamin B 12
/ metabolism
Vitamins
/ metabolism
DTT
Methionine
Methyltransferase
Reductive stress
Vitamin B12
Journal
BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720
Informations de publication
Date de publication:
08 10 2022
08 10 2022
Historique:
received:
03
05
2022
accepted:
20
09
2022
entrez:
8
10
2022
pubmed:
9
10
2022
medline:
12
10
2022
Statut:
epublish
Résumé
One-carbon metabolism, which includes the folate and methionine cycles, involves the transfer of methyl groups which are then utilised as a part of multiple physiological processes including redox defence. During the methionine cycle, the vitamin B12-dependent enzyme methionine synthetase converts homocysteine to methionine. The enzyme S-adenosylmethionine (SAM) synthetase then uses methionine in the production of the reactive methyl carrier SAM. SAM-binding methyltransferases then utilise SAM as a cofactor to methylate proteins, small molecules, lipids, and nucleic acids. We describe a novel SAM methyltransferase, RIPS-1, which was the single gene identified from forward genetic screens in Caenorhabditis elegans looking for resistance to lethal concentrations of the thiol-reducing agent dithiothreitol (DTT). As well as RIPS-1 mutation, we show that in wild-type worms, DTT toxicity can be overcome by modulating vitamin B12 levels, either by using growth media and/or bacterial food that provide higher levels of vitamin B12 or by vitamin B12 supplementation. We show that active methionine synthetase is required for vitamin B12-mediated DTT resistance in wild types but is not required for resistance resulting from RIPS-1 mutation and that susceptibility to DTT is partially suppressed by methionine supplementation. A targeted RNAi modifier screen identified the mitochondrial enzyme methylmalonyl-CoA epimerase as a strong genetic enhancer of DTT resistance in a RIPS-1 mutant. We show that RIPS-1 is expressed in the intestinal and hypodermal tissues of the nematode and that treating with DTT, β-mercaptoethanol, or hydrogen sulfide induces RIPS-1 expression. We demonstrate that RIPS-1 expression is controlled by the hypoxia-inducible factor pathway and that homologues of RIPS-1 are found in a small subset of eukaryotes and bacteria, many of which can adapt to fluctuations in environmental oxygen levels. This work highlights the central importance of dietary vitamin B12 in normal metabolic processes in C. elegans, defines a new role for this vitamin in countering reductive stress, and identifies RIPS-1 as a novel methyltransferase in the methionine cycle.
Sections du résumé
BACKGROUND
One-carbon metabolism, which includes the folate and methionine cycles, involves the transfer of methyl groups which are then utilised as a part of multiple physiological processes including redox defence. During the methionine cycle, the vitamin B12-dependent enzyme methionine synthetase converts homocysteine to methionine. The enzyme S-adenosylmethionine (SAM) synthetase then uses methionine in the production of the reactive methyl carrier SAM. SAM-binding methyltransferases then utilise SAM as a cofactor to methylate proteins, small molecules, lipids, and nucleic acids.
RESULTS
We describe a novel SAM methyltransferase, RIPS-1, which was the single gene identified from forward genetic screens in Caenorhabditis elegans looking for resistance to lethal concentrations of the thiol-reducing agent dithiothreitol (DTT). As well as RIPS-1 mutation, we show that in wild-type worms, DTT toxicity can be overcome by modulating vitamin B12 levels, either by using growth media and/or bacterial food that provide higher levels of vitamin B12 or by vitamin B12 supplementation. We show that active methionine synthetase is required for vitamin B12-mediated DTT resistance in wild types but is not required for resistance resulting from RIPS-1 mutation and that susceptibility to DTT is partially suppressed by methionine supplementation. A targeted RNAi modifier screen identified the mitochondrial enzyme methylmalonyl-CoA epimerase as a strong genetic enhancer of DTT resistance in a RIPS-1 mutant. We show that RIPS-1 is expressed in the intestinal and hypodermal tissues of the nematode and that treating with DTT, β-mercaptoethanol, or hydrogen sulfide induces RIPS-1 expression. We demonstrate that RIPS-1 expression is controlled by the hypoxia-inducible factor pathway and that homologues of RIPS-1 are found in a small subset of eukaryotes and bacteria, many of which can adapt to fluctuations in environmental oxygen levels.
CONCLUSIONS
This work highlights the central importance of dietary vitamin B12 in normal metabolic processes in C. elegans, defines a new role for this vitamin in countering reductive stress, and identifies RIPS-1 as a novel methyltransferase in the methionine cycle.
Identifiants
pubmed: 36209095
doi: 10.1186/s12915-022-01415-y
pii: 10.1186/s12915-022-01415-y
pmc: PMC9548181
doi:
Substances chimiques
Lipids
0
Nucleic Acids
0
Reducing Agents
0
Sulfhydryl Compounds
0
Vitamins
0
Homocysteine
0LVT1QZ0BA
Mercaptoethanol
60-24-2
Carbon
7440-44-0
S-Adenosylmethionine
7LP2MPO46S
Folic Acid
935E97BOY8
Methionine
AE28F7PNPL
Methyltransferases
EC 2.1.1.-
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
EC 2.1.1.13
Ligases
EC 6.-
Vitamin B 12
P6YC3EG204
Oxygen
S88TT14065
Dithiothreitol
T8ID5YZU6Y
Hydrogen Sulfide
YY9FVM7NSN
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
228Subventions
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/K006983/1
Pays : United Kingdom
Informations de copyright
© 2022. The Author(s).
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