The TRM10 family includes three distinct homologs in humans: TRMT10A, TRMT10B, and TRMT10C. Each homolog exhibits unique substrate specificities and subcellular localizations, necessitating specialized antibodies for their detection.
TRMT10A is the primary enzyme responsible for m1G9 modifications in cytosolic tRNAs, critical for translation fidelity . Its deficiency correlates with impaired glucose metabolism and microcephaly .
TRMT10B uniquely catalyzes m1A9 modifications in tRNA Asp, as demonstrated by HPLC-MS/MS analysis .
TRMT10C is essential for mitochondrial tRNA 5'-end processing and respiration. Mutations in TRMT10C are linked to mitochondrial diseases .
Deletion of TRMT10A in yeast leads to hypersensitivity to 5-fluorouracil (5FU), a chemotherapeutic agent, due to reduced tRNA Trp levels .
TRMT10C mutations impair mitochondrial translation, highlighting its role in energy metabolism .
TRM10 antibodies enable:
KEGG: sce:YOL093W
STRING: 4932.YOL093W