Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
-
SwissProt keyword-derived (SPKW) annotations present in the Sept 2025 goa_uniprot_gcrp snapshot but removed from the current GOA release after GOA retired the keyword2GO pipeline for cellular organisms.
-
For MET1A, the keyword "Methyltransferase" mapped to the bare process term "methylation" (GO:0032259), which drops the substrate (DNA) and the C5-cytosine / maintenance specificity; the substrate-specific process is GO:0141119.
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Characterization of two rice DNA methyltransferase genes and RNAi-mediated reactivation of a silenced transgene in rice callus.
-
OsMET1-1 (MET1A) and OsMET1-2 each encode a cytosine-5 DNA methyltransferase of the Dnmt1/MET1 class, with two-thirds regulatory and one-third catalytic domain.
-
Steady-state OsMET1-2 mRNA is 7- to 12-fold higher than OsMET1-1 in callus, root and inflorescence, indicating OsMET1a is the minor, lower-expressed paralog.
-
RNAi knockdown of OsMET1-1 reactivated a silenced 35S-uidA-nos transgene in rice callus, consistent with inactivation of maintenance methylation and the involvement of methylation in transcriptional silencing.
Collection, mapping, and annotation of over 28,000 cDNA clones from japonica rice.
Deep-research report (falcon / Edison Scientific Literature) - functional annotation of rice MET1A (Q7Y1I7).
-
MET1A (OsMET1a / OsMET1-1; LOC_Os03g58400) is a DNMT1-like maintenance DNA (cytosine-5) methyltransferase (EC 2.1.1.37) that transfers a methyl group to the C5 position of cytosine in DNA, primarily maintaining symmetric CG methylation after replication.
-
Rice CG methylation is mainly maintained by MET1 enzymes (OsMET1a and OsMET1b); OsMET1b is the dominant, more highly expressed paralog, and an OsMET1-1 knock-in mutant showed no discernible developmental phenotype, indicating a minor/redundant role for OsMET1a.
-
Loss of the major paralog OsMET1b collapses gene-body mCG from 27.35% to 3.95% (~86% loss), reduces transposon mCG ~77%, derepresses transposons, and co-induces OsMET1a ~2.5-fold and a VIM-family cofactor ~4.5-fold, placing OsMET1a in the CG-maintenance machinery and its buffering responses.
-
A maintenance DNA methyltransferase acting on chromosomal DNA is most plausibly nuclear; no direct OsMET1a localization or in vitro substrate-preference assay was retrieved, so these are inferences from enzyme class and orthology.