“…A common defect of the reproductive branch is that its subtending leaf (bract) is de-repressed, which can be taken as the marker event to evaluate the heterochronic-vegetative growth during reproductive organogenesis (Kawakatsu et al, 2009). Several genes underlying bract suppression have been isolated in Arabidopsis, maize, rice, barley, and wheat; these genes differ between monocotyledon and dicotyledon plants (Chuck et al, 2007(Chuck et al, , 2010Ferrandiz et al, 2000;Hepworth et al, 2006;Houston et al, 2012;Ikeda et al, 2019;Karim et al, 2009;Kawakatsu et al, 2006Kawakatsu et al, , 2009Li et al, 2019;Miyoshi et al, 2004;Muller-Xing et al, 2014;Ohno et al, 2004;Park et al, 2007;Sauret-Gueto et al, 2013;Walla et al, 2020;Wang et al, 2009b;Weigel et al, 1992;Whipple et al, 2010), indicating that the transition between vegetative and reproductive branches may be controlled by lineage-specific genes. Besides leaf outgrowth, flowers are converted into the leafy shoots in the bract de-repression mutants ap1 cal ful, puchi bop1 bop2, and lfy in Arabidopsis (Ferrandiz et al, 2000;Karim et al, 2009;Weigel et al, 1992), while panicle branches are transformed into the leafy shoots in the bract derepression mutants plastochron1 (pla1), pla2/leafy head2 (lhd2), and pla3 in rice (supplemental Figure 1D and 1E) (Itoh et al, 1998;Miyoshi et al, 2004;Kawakatsu et al, 2006Kawakatsu et al, , 2009Xiong et al, 2006), implying that bract suppression is in general tightly linked to the irreversible developmental patterns of the reproductive branches.…”