Peptide signaling in plants.

I plants, only a few peptides have been identified that act as signaling molecules (1). In contrast, signaling peptides are major players in all aspects of the life cycle in animals and yeast (2), suggesting that signaling mechanisms across the eukaryotic kingdom are fundamentally different. In animals and yeast, signaling peptides are synthesized, in general, as part of longer biologically inactive preproproteins, from which they are released by specific proteases. The few signaling peptides studied in plants so far indicate that plants do not follow a similar approach to generate peptides. In a recent issue of PNAS, however, a tobacco polypeptide is described, showing the typical features of a stereotypical preproprotein from which an active signaling peptide, called rapid alkalinization factor (RALF), is released (3). RALF is a 5-kDa peptide that is located at the C terminus of a 115-aa long preproprotein. The peptide was identified in a bioassay involving a suspension culture of tobacco cells (3). Very recently (4), this assay also resulted in the identification of two other tobacco peptides, tobacco systemin I and II (Tob sysI and -II). Additionally, their synthesis revealed high similarities to peptide synthesis in animals and yeast. Our knowledge of peptide signaling in plants was built on the properties of the five peptides discovered so far: tomato systemin, PSK, ENOD40, CLV3, and SCR (1). The latter two are small proteins of 72–75 aa and 53–55 aa, respectively, of which the primary translation products contain an N-terminal hydrophobic stretch that serves as a leader sequence for secretion (5, 6). The ENOD40 primary translation product consists of 10–13 amino acids (7). It is unlikely that CLV3, SCR, or ENOD40 are subject to proteolytic processing to release the biologically active peptide. It has been shown that the active peptides for tomato systemin and Oryza sativa PSK are released from a preproprotein by proteolytic processing (8, 9). However, which proteases are involved and their specificity are not known yet. Only the OsPSK proprotein has an N-terminal leader sequence (9). With the discovery of RALF and Tob sysI and -II, examples of more stereotypical preproproteins in plants have now become available. Tomato systemin is the first identified plant signaling peptide. It is composed of 18 amino acids and is able to confer a systemic wounding response in tomato plants attacked by herbivores (8). Although more than 100 diverse plant species respond systemically to herbivore attacks (10), homologues of systemin could be identified only in some other Solanaceae (11), but strikingly, not in tobacco, which also belongs to the Solanaceae. It was known that tomato systemin could activate a mitogenactivated protein (MAP) kinase in suspension culture cells and induce an alkalinization of the medium (12). In tomato plants, tomato systemin is able to induce expression of proteinase-inhibitor protein-encoding genes (8). These properties of tomato systemin have been exploited to search for a peptide with systemin-like properties in extracts of herbivoreattacked tobacco leaves using a tobacco suspension culture. By using this assay, two peptides from tobacco were identified that matched all of the criteria for being tobacco systemin analogues and were, therefore, called Tob sysI and Tob sysII (4). Their sequence is not homologous to the tomato systemin, but their function is homologous. From these facts, it can be inferred that structurally diverse peptides in different plant species, although belonging to the same family, can have similar functions, an observation not yet made in animals and yeast. The two tobacco systemin peptides are integral parts of a single precursor preproprotein that has an N-terminal leader sequence for translocation via the secretory pathway. The presence of multiple peptides within one precursor molecule is common in animals and yeast, but tobacco systemin is the first example found in plants. During the purification of Tob sysI and -II, RALF was identified as a peptide; like systemin, RALF is able to activate MAP kinase and to induce alkalinization of the medium, albeit in a much faster way (3). Therefore, it was named rapid alkalinization factor. In contrast to Tob sysI and -II, RALF does not induce proteinase-inhibitor gene expression in plants (3) and, thus, is not a systemin. RALF is part of a preproprotein that contains the typical dibasic motif that, in animals and yeast hormone preproproteins, is recognized by specific Ser proteases for the release of the active peptide (13). Therefore, the RALF-containing preproprotein most likely is processed by a Ser protease. In plants, proteins homologous to subtilisin-like proteases, belonging to the super family of Ser proteases, are widespread, but for none of these is