Mobility of Antiflorigen and PEBP mRNAs in Tomato-Tobacco Heterografts

Abstract

Photoperiodic floral induction is controlled by the leaf-derived and antagonistic mobile signals florigen and antiflorigen. In response to photoperiodic variations, florigen and antiflorigen are produced in leaves and translocated through phloem to the apex, where they counteract floral initiation. Florigen and antiflorigen are encoded by a pair of homologs belonging to FLOWERING LOCUS T (FT)- or TERMINAL FLOWER1 (TFL1)-like clades in the phosphatidylethanolamine-binding domain protein (PEBP) family. The PEBP gene family contains FT-, TFL1-, and MOTHER OF FT AND TFL1 (MFT)-like clades. Evolutionary analysis suggests that FT- and TFL1-like clades arose from an ancient MFT-like clade. The protein movement of the PEBP family is an evolutionarily conserved mechanism in many plants; however, the mRNA movement of the PEBP family remains controversial. Here, we examined the mRNA movement of PEBP genes in different plant species. We identified a tobacco (Nicotiana sylvestris) CENTRORADIALIS-like1 gene, denoted NsCET1, and showed that NsCET1 is an ortholog of the Arabidopsis (Arabidopsis thaliana) antiflorigen ATC In tobacco, NsCET1 acts as a mobile molecule that non-cell-autonomously inhibits flowering. Grafting experiments showed that endogenous and ectopically expressed NsCET1 mRNAs move long distances in tobacco and Arabidopsis. Heterografts of tobacco and tomato (Solanum lycopersicum) showed that, in addition to NsCET1, multiple members of the FT-, TFL1-, and MFT-like clades of tobacco and tomato PEBP gene families are mobile mRNAs. Our results suggest that the mRNA mobility is a common feature of the three clades of PEBP-like genes among different plant species.