Abstract
Shoot apical meristem is a well organized undifferentiated tissue which produces plant body. CLV3 peptide hormone regulates SAM homeostasis, and is perceived by several receptor complexes, CLV1, CLV2-SOL2/CRN and RPK2. CLV1 homologues are encoded in various plants genome. However CLV2 and SOL2/CRN homologues are found only in higher plants. Here we show that the RPK2 homologues were found not only in moss, Physcomitrella patens, but also in liverwort, Marchantia polymorpha. Although CLV2-SOL2/CRN might have specific function in SAM homeostasis, CLV1 and RPK2 may regulate various plant physiological events during plant evolution.
Key words: RPK2, SOL2, CLE, CLV, CRN, meristem, receptor kinase
In higher plants, the CLV signaling pathway regulates meristem fate in a noncellautonomous manner. CLV3 is one of the 32 members of the CLV3/ESR-related (CLE) gene family in Arabidopsis, and CLV3 functions as a dodecapeptide1,2 that functions as an intercellular signaling molecule to repress the expression of the homeobox transcription factor WUS in the organization center. In this signaling pathway, receptor complexes CLV1 and CLV2-SOL2/CRN perceive the CLV3 peptide ligand. The suppression of WUS expression leads to the restriction of the stem cell population in the SAM and balances cell proliferation and differentiation. Recently we isolated RPK2 as a third receptor of the CLV3 signal in Arabidopsis. So, at least three receptors, CLV1, CLV2-SOL2/CRN and RPK2 are responsible for CLV3 perception for SAM maintenance system in Arabidopsis.3–7
CLE peptides are considered to function in plant morphogenesis as intercellular signaling molecules,8–14 and CLE genes have been found in various seed plants and even in the moss Physcomitrella patens.2,15–18 As for the receptors, CLV1 homologues were identified not only in vascular plants but also in the bryophyte Physcomitrella.18 However, CLV2 and SOL2/CRN homologues were found only in higher plants, and were not found in the genomes of Selaginella moelendorffii or Physcomitrella patens.18
To identify RPK2 homologues in plants, we performed BLAST search. RPK2 homologues were found not only from seed plants but also from moss, Physcomitrella patens, and from liverwort, Marchantia polymorpha. Only one homolog was found from moss and liverwort. However, most of other higher plants have multiple homologues. This result indicates that the RPK2 homologues are responsible for many physiological events in higher plants.
Our phylogenetic analysis indicates that RPK2 and CLV1 have evolved from early evolutional steps in plants. On the other hand, CLV2 and SOL2/CRN homologues were found as a single gene only in higher plants, indicating that they have specific functions in multicellular organisms. CLV2 and SOL2/CRN might be necessary to evolve complex multicellular SAM structure in plants.
Functional diversity of RPK2 and CLV1 homologues remains to be resolved. The existence of a number of RPK2 and CLV1 homologues among higher plants implies a functional diversity among them. Except for the functions of CLV3 and TDIF, the functions of most CLE peptides are largely unknown. The direct interaction between CLE peptides and their cognate receptors will be examined with a biochemical approach because it is possible that these receptors bind other ligands. Further genetic and biochemical studies of these receptor-like proteins in various plant species will provide further evidence for CLE peptide and receptor functions in various aspects of plant development.
Figure 1.

A neighbor-joining tree of RPK2. Protein sequence of RPK2 homologues of Arabidopsis thaliana (RPK2 and CLV1 as an out group), Musa acuminata (MaRPK2: ABF72006.1), Oryza sativa Indica Group (OsIRPK21: EAY91907.1, OsIRPK22: EAZ04623.1), Oryza sativa Japonica Group (OsJRPK21: NP_001051315.1, OsJRPK22: NP_001060207.1), Populus trichocarpa (PtRPK21: XP_002305358.1, PtRPK22: XP_002311344.1, PtRPK23: XP_002321080.1, PtRPK24: XP_002323902.1), Vitis vinifera (VvRPK21: CAN67126.1, VvRPK22: CAN77668.1, VvRPK23: CAO40245.1, VvRPK24: CAO41857.1, VvRPK25: CAO49170.1, VvRPK26: XP_002274047.1, VvRPK27: XP_002274211.1, VvRPK28: XP_002276030.1, VvRPK29: XP_002279979.1), Sorghum bicolor (SbRPK21: XP_002460974.1, SbRPK22: XP_002462751.1, SbRPK23 XP_002463860.1), Ricinus communis (RcRPK21: XP_002512071.1, RcRPK22: XP_002512822.1, RcRPK23: XP_002515143.1, RcRPK24: XP_002527617.1), Physcomitrella patens (PpRPK2: XP_001781758.1) and Marchantia polymorpha (MpRPK2: isotig22424), were used to construct the phylogenic tree. Bootstrap values of 60% and above, from the neighbor-joining method with Kimura's correction, are shown. The scale bar indicates the number of amino acid substitutions per site.
Abbreviations
- CLE
CLAVATA3/ESR-related
- SAM
shoot apical meristem
- RAM
root apical meristem
- WUS
wuschel
- CLV
clavata
- LRR
leucin rich repeat
- CRN
coryne
- SOL2
suppressor of LLP1 2
- RPK2
receptor like protein kinase 2
- MaRPK2
Musa acuminata RPK2-like protein
- OsIRPK2
Oryza sativa indica group RPK2-like protein
- OsJRPK2
Oryza sativa japonica group RPK2-like protein
- PtRPK2
Populus trichocarpa RPK2-like protein
- VvRPK21
Vitis vinifera RPK2-like protein
- SbRPK2
Sorghum bicolor RPK2-like protein
- RcRPK2
Ricinus communis RPK2-like protein
- PpRPK2
Physcomitrella patens RPK2-like protein
- MpRPK2
Marchantia polymorpha RPK2-like protein
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