the shoot apex and activates transcription of meristem identity genes such as APETALA1 (AP1). 10,11 Recent studies from several laboratories have provided strong evidence for the FT protein in Arabidopsis and corresponding proteins in other species being an important part of the florigen. [12][13][14][15][16] These were mainly based on (1) detection in the shoot apex or its vicinity of GFP-fusion or Myc-tagged proteins expressed by promoters with preferential activity in the phloem tissues in Arabidopsis and rice, 12-14 (2) detection of FT-like proteins in the phloem sap from cucurbits, 16 and (3) transmission of FT:GFP protein through a graft junction from donor transgenic plants expressing the fusion protein in the vasculature to recipient ft plants with concomitant promotion of flowering. 12 Because key observations in Arabidopsis 12,14 were based on the effect of cumulative expression by SUCROSE TRANSPORTER 2 (SUC2) promoter which has strong activity in the vasculature within a short distance from the shoot, 12,14,17 it is difficult to analyze the temporal aspects of the transport and to exclude the possibility of short-distance, cellto-cell transport without entering into the phloem. In addition, the ability of GFP for long-distance transport via the phloem and a graft junction 18,19 makes an independent confirmation based on methods other than GFP-fusion protein desirable.Our recent work aimed to resolve these difficulties by the combined use of FT-T7 protein, a local transient induction system, and a two-shoot "Y-grafting" technique originally described by Turnbull and colleagues. 20 Since graft-transmission has been an important criterion of florigen, we first demonstrated the grafttransmissible action of FT both from the endogenous gene and transgenes under the control of 35S promoter and SULPHATE TRANSPORTER 2;1 (SULTR2;1) promoter with preferential expression in the phloem. 19,21 Grafting of a wild-type scion resulted in small but significant reduction in both days to flowering and the number of leaves at flowering of recipient ft-1 stock plants, while grafting of a strong 35S::FT scion caused much greater (more than 20 leaves) reduction (Fig. 1A). Even in the latter case, rescue may sound rather modest, since the recipient ft-1 stock plants still had 20 more leaves than the intact wild-type plants grown in the same conditions. 21 However, given that functional connection of phloem capable of trafficking tracer dyes and enhanced GFP (EGFP) were established about 2 weeks after grafting, by which time wild-type plants made [Plant Signaling & Behavior 4:2, 123-125; February 2009] Seasonal flowering is an important adaptive trait in plants for reproductive success. Plants monitor day length in the leaf to anticipate upcoming seasonal changes and initiate floral morphogenesis at the shoot apex by the action of the leaf-generated mobile florigen. 1-3 FT, a 20-kDa protein, is a conserved potent promoter of flowering. [4][5][6][7] In Arabidopsis, transcription of FT is induced by long days in the phloem tissu...