CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development

The CLAVATA pathway plays a key role in the regulation of multicellular shoot and root meristems in flowering plants. In Arabidopsis, CLAVATA 3-like signaling peptides (CLEs) act via receptor-like kinases CLAVATA 1 and CRINKLY 4 (CR4). In the moss Physcomitrium patens, PpCLAVATA and PpCR4 were previ...

Full description

Saved in:
Bibliographic Details
Main Authors: Alain Shumbusho, C. Jill Harrison, Viktor Demko
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Plant Signaling & Behavior
Subjects:
Online Access:http://dx.doi.org/10.1080/15592324.2024.2386502
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846095052183437312
author Alain Shumbusho
C. Jill Harrison
Viktor Demko
author_facet Alain Shumbusho
C. Jill Harrison
Viktor Demko
author_sort Alain Shumbusho
collection DOAJ
description The CLAVATA pathway plays a key role in the regulation of multicellular shoot and root meristems in flowering plants. In Arabidopsis, CLAVATA 3-like signaling peptides (CLEs) act via receptor-like kinases CLAVATA 1 and CRINKLY 4 (CR4). In the moss Physcomitrium patens, PpCLAVATA and PpCR4 were previously studied independently and shown to play conserved roles in the regulation of cell proliferation and differentiation. The plant calpain DEFECTIVE KERNEL 1 (DEK1) has been identified as another key regulator of cell division and cell fate in vascular plants and bryophytes. The functional interaction between CLAVATA, CR4, and DEK1 remains unknown. Here, we show that P. patens crinkly4 and dek1 mutants respond differently to CLE peptide treatments suggesting their distinct roles in the CLAVATA pathway. Reduced CLAVATA-mediated suppression of leafy shoot growth in Δcr4 mutants indicates that PpCR4 is involved in CLV3p perception, most likely as a receptor. The CLV3p strongly suppressed leaf vein development in Δcr4 mutants, suggesting that other receptors are involved in these processes and indicating a potential role of PpCR4 in organ sensitization to CLEs.
format Article
id doaj-art-d60c4c2a255240749aed6f9fc4200e82
institution Kabale University
issn 1559-2316
1559-2324
language English
publishDate 2024-12-01
publisher Taylor & Francis Group
record_format Article
series Plant Signaling & Behavior
spelling doaj-art-d60c4c2a255240749aed6f9fc4200e822025-01-02T11:44:27ZengTaylor & Francis GroupPlant Signaling & Behavior1559-23161559-23242024-12-0119110.1080/15592324.2024.23865022386502CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore developmentAlain Shumbusho0C. Jill Harrison1Viktor Demko2Comenius University in BratislavaUniversity of BristolComenius University in BratislavaThe CLAVATA pathway plays a key role in the regulation of multicellular shoot and root meristems in flowering plants. In Arabidopsis, CLAVATA 3-like signaling peptides (CLEs) act via receptor-like kinases CLAVATA 1 and CRINKLY 4 (CR4). In the moss Physcomitrium patens, PpCLAVATA and PpCR4 were previously studied independently and shown to play conserved roles in the regulation of cell proliferation and differentiation. The plant calpain DEFECTIVE KERNEL 1 (DEK1) has been identified as another key regulator of cell division and cell fate in vascular plants and bryophytes. The functional interaction between CLAVATA, CR4, and DEK1 remains unknown. Here, we show that P. patens crinkly4 and dek1 mutants respond differently to CLE peptide treatments suggesting their distinct roles in the CLAVATA pathway. Reduced CLAVATA-mediated suppression of leafy shoot growth in Δcr4 mutants indicates that PpCR4 is involved in CLV3p perception, most likely as a receptor. The CLV3p strongly suppressed leaf vein development in Δcr4 mutants, suggesting that other receptors are involved in these processes and indicating a potential role of PpCR4 in organ sensitization to CLEs.http://dx.doi.org/10.1080/15592324.2024.2386502cell-to-cell signalingclavataleaf developmentphyscomitrium patenscrinkly4 kinasedefective kernel
spellingShingle Alain Shumbusho
C. Jill Harrison
Viktor Demko
CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
Plant Signaling & Behavior
cell-to-cell signaling
clavata
leaf development
physcomitrium patens
crinkly4 kinase
defective kernel
title CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
title_full CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
title_fullStr CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
title_full_unstemmed CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
title_short CLE peptides act via the receptor-like kinase CRINKLY 4 in Physcomitrium patens gametophore development
title_sort cle peptides act via the receptor like kinase crinkly 4 in physcomitrium patens gametophore development
topic cell-to-cell signaling
clavata
leaf development
physcomitrium patens
crinkly4 kinase
defective kernel
url http://dx.doi.org/10.1080/15592324.2024.2386502
work_keys_str_mv AT alainshumbusho clepeptidesactviathereceptorlikekinasecrinkly4inphyscomitriumpatensgametophoredevelopment
AT cjillharrison clepeptidesactviathereceptorlikekinasecrinkly4inphyscomitriumpatensgametophoredevelopment
AT viktordemko clepeptidesactviathereceptorlikekinasecrinkly4inphyscomitriumpatensgametophoredevelopment