Abstract

BackgroundIn flowering plants, precise timing of the floral transition is crucial to maximize chances of reproductive success, and as such, this process has been intensively studied. FLOWERING LOCUS T (FT) and TERMINAL FLOWER1 (TFL1) have been identified as closely related eukaryotic phosphatidylethanolamine-binding proteins (‘EuPEBPs’) that integrate multiple environmental stimuli, and act antagonistically to determine the optimal timing of the floral transition. Extensive research has demonstrated that FT acts similar to hormonal signals, being transported in the phloem from its primary site of expression in leaves to its primary site of action in the shoot meristem; TFL1 also appears to act as a mobile signal. Recent work implicates FT, TFL1, and the other members of the EuPEBP family, in the control of other important processes, suggesting that the EuPEBP family may be key general regulators of developmental transitions in flowering plants. In eudicots, there are a small number of EuPEBP proteins, but in monocots, and particularly grasses, there has been a large, but uncharacterized expansion of EuPEBP copy number, with unknown consequences for the EuPEBP function.ResultsTo systematically characterize the evolution of EuPEBP proteins in flowering plants, and in land plants more generally, we performed a high-resolution phylogenetic analysis of 701 PEBP sequences from 208 species. We refine previous models of EuPEBP evolution in early land plants, demonstrating the algal origin of the family, and pin-pointing the origin of the FT/TFL1 clade at the base of monilophytes. We demonstrate how a core set of genes (MFT1, MFT2, FT, and TCB) at the base of flowering plants has undergone differential evolution in the major angiosperm lineages. This includes the radical expansion of the FT family in monocots into 5 core lineages, further re-duplicated in the grass family to 12 conserved clades.ConclusionsWe show that many grass FT proteins are strongly divergent from other FTs and are likely neo-functional regulators of development. Our analysis shows that monocots and eudicots have strongly divergent patterns of EuPEBP evolution.

Highlights

  • In flowering plants, precise timing of the floral transition is crucial to maximize chances of reproductive success, and as such, this process has been intensively studied

  • We have investigated the complex patterns of eukaryotic phosphatidylethanolamine-binding proteins (EuPEBPs) evolution in angiosperms and how these differ between monocots and eudicots

  • Canonical EuPEBP proteins are found across the streptophyte lineage To understand the evolution of the EuPEBP family with greater resolution, we obtained 701 sequences from 208 species, covering all major land plants groups, including charophyte algae

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Summary

Introduction

Precise timing of the floral transition is crucial to maximize chances of reproductive success, and as such, this process has been intensively studied. Extensive research has demonstrated that FT acts similar to hormonal signals, being transported in the phloem from its primary site of expression in leaves to its primary site of action in the shoot meristem; TFL1 appears to act as a mobile signal. Extensive research has demonstrated that FT acts similar to a hormone, being transported in the phloem from its primary site of expression in leaves to its primary site of action in the shoot meristem [3] As such, it has been identified as a key contributor to the mobile ‘florigen’ signal, identified in the 1930s by grafting studies [4]. The FT gene acts as a hub for environmental signal integration in leaves, while the FT protein acts in shoot meristems to induce the change from the vegetative to the reproductive developmental program in newly formed tissues

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