<P>ATMS1 plays a key role in regulating DNA and histone methylations by its function in the one-carbon metabolism pathway.</P><P>DNA methylation and histone modification are important epigenetic marks that coregulate gene expression and genome stability. To identify factors involved in chromatin silencing, we carried out a forward genetic screen for mutants that release the silenced <I>Pro-35S</I>:<I>LUCIFERASE</I> (<I>35SP-LUC</I>) in Arabidopsis (<I>Arabidopsis thaliana</I>). We identified an epigenetic regulator, METHIONINE SYNTHASE1 (ATMS1), which catalyzes the synthesis of methionine (Met) in the one-carbon metabolism pathway. The <I>ATMS1</I> mutation releases the silenced <I>35SP-LUC</I> and the majority of endogenous genes and transposons. The effect of <I>ATMS1</I> on chromatin silencing is related to decreased levels of DNA methylation (CG, CHG, and CHH) and histone-3 lysine-9 dimethylation. The <I>ATMS1</I> mutation caused a significant decrease in the ratio of <I>S</I>-adenosylmethionine to <I>S</I>-adenosylhomocysteine. Exogenous application of Met rescued the phenotype of <I>atms1-1</I>. ATMS1 plays a predominant role in DNA and histone methylations among the three Met synthetase homologs. These results suggest that ATMS1 is required for DNA and histone methylations through its function in the one-carbon metabolism pathway, indicating the complex interplay between metabolism and epigenetic regulation.</P>