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However, Medicago lacks <jats:italic>FLC<\/jats:italic> and <jats:italic>CO<\/jats:italic>, key regulators of Arabidopsis VLD flowering<jats:italic>.<\/jats:italic> Most plants have two <jats:italic>INHIBITOR OF GROWTH<\/jats:italic> (<jats:italic>ING<\/jats:italic>) genes (<jats:italic>ING1<\/jats:italic> and <jats:italic>ING2<\/jats:italic>), encoding proteins with an ING domain with two anti\u2010parallel alpha\u2010helices and a plant homeodomain (PHD) finger, but their genetic role has not been previously described<jats:italic>.<\/jats:italic> In Medicago, <jats:italic>Mting1<\/jats:italic> gene\u2010edited mutants developed and flowered normally, but an <jats:italic>Mting2\u20101 Tnt1<\/jats:italic> insertion mutant and gene\u2010edited <jats:italic>Mting2<\/jats:italic> mutants had developmental abnormalities including delayed flowering particularly in VLD, compact architecture, abnormal leaves with extra leaflets but no trichomes, and smaller seeds and barrels. <jats:italic>Mting2<\/jats:italic> mutants had reduced expression of activators of flowering, including the <jats:italic>FT<\/jats:italic>\u2010like gene <jats:italic>MtFTa1<\/jats:italic>, and increased expression of the candidate repressor <jats:italic>MtTFL1c<\/jats:italic>, consistent with the delayed flowering of the mutant. <jats:italic>MtING2<\/jats:italic> overexpression complemented <jats:italic>Mting2\u20101<\/jats:italic>, but did not accelerate flowering in wild type. The MtING2 PHD finger bound H3K4me2\/3 peptides weakly <jats:italic>in\u2009vitro<\/jats:italic>, but analysis of gene\u2010edited mutants indicated that it was dispensable to MtING2 function in wild\u2010type plants. RNA sequencing experiments indicated that &gt;7000 genes are mis\u2010expressed in the <jats:italic>Mting2\u20101<\/jats:italic> mutant, consistent with its strong mutant phenotypes. Interestingly, ChIP\u2010seq analysis identified &gt;5000 novel H3K4me3 locations in the genome of <jats:italic>Mting2\u20101<\/jats:italic> mutants compared to wild type R108. 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