Skip to main content
. 2019 Dec;7(24):797. doi: 10.21037/atm.2019.12.65

Table 1. m6A modulator families.

Family Abbreviation Name Function Forward primer Reverse primer
The “writers” of m6A modification METTL3 Methyltransferase-like 3 METTL14, METTL3 form m6A methyltransferase complex. WTAP guided and localized the METTL3–METTL14 complex into nuclear speckles to efficiently methylate target RNAs TTGTCTCCAACCTTCCGTAGT CCAGATCAGAGAGGTGGTGTAG
METTL14 Methyltransferase-like 14 GAACACAGAGCTTAAATCCCCA TGTCAGCTAAACCTACATCCCTG
The “readers” of m6A modification YTHDF1 YT521-B homology F1 YTHDF proteins directly bind and recognize m6A methylation on mRNAs, spatiotemporal control over RNA metabolism in a collaborative way; YTHDF1 can stimulate the translation of target mRNA, while YTHDF2 promotes mRNA decay; YTHDF3 regulates RNA metabolism ACCTGTCCAGCTATTACCCG TGGTGAGGTATGGAATCGGAG
YTHDF2 YT521-B homology F2 AGCCCCACTTCCTACCAGATG TGAGAACTGTTATTTCCCCATGC
YTHDF3 YT521B homology F3 GCTATCCACCTAGTTCTCTTGGG ATGCCAGGCACCTTACTCAAA
The “erasers” of m6A modification FTO Fat mass and obesity-associated protein FTO is the first enzyme identified to demethylate RNA m3U and m6A AACACCAGGCTCTTTACGGTC TGTCCGTTGTAGGATGAACCC
ALKBH5 AlkB homolog 5 ALKBH5 might serve as another demethylase and regulate m6A in mRNAs CGGCGAAGGCTACACTTACG CCACCAGCTTTTGGATCACCA

m6A, N6-methyladenosine; mRNA, messenger RNA; m3U, 3-methyluridine.