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Bioinformatic analysis of the CLE signaling peptide family

BACKGROUND: Plants encode a large number of leucine-rich repeat receptor-like kinases. Legumes encode several LRR-RLK linked to the process of root nodule formation, the ligands of which are unknown. To identify ligands for these receptors, we used a combination of profile hidden Markov models and p...

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Autores principales: Oelkers, Karsten, Goffard, Nicolas, Weiller, Georg F, Gresshoff, Peter M, Mathesius, Ulrike, Frickey, Tancred
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254619/
https://www.ncbi.nlm.nih.gov/pubmed/18171480
http://dx.doi.org/10.1186/1471-2229-8-1
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author Oelkers, Karsten
Goffard, Nicolas
Weiller, Georg F
Gresshoff, Peter M
Mathesius, Ulrike
Frickey, Tancred
author_facet Oelkers, Karsten
Goffard, Nicolas
Weiller, Georg F
Gresshoff, Peter M
Mathesius, Ulrike
Frickey, Tancred
author_sort Oelkers, Karsten
collection PubMed
description BACKGROUND: Plants encode a large number of leucine-rich repeat receptor-like kinases. Legumes encode several LRR-RLK linked to the process of root nodule formation, the ligands of which are unknown. To identify ligands for these receptors, we used a combination of profile hidden Markov models and position-specific iterative BLAST, allowing us to detect new members of the CLV3/ESR (CLE) protein family from publicly available sequence databases. RESULTS: We identified 114 new members of the CLE protein family from various plant species, as well as five protein sequences containing multiple CLE domains. We were able to cluster the CLE domain proteins into 13 distinct groups based on their pairwise similarities in the primary CLE motif. In addition, we identified secondary motifs that coincide with our sequence clusters. The groupings based on the CLE motifs correlate with known biological functions of CLE signaling peptides and are analogous to groupings based on phylogenetic analysis and ectopic overexpression studies. We tested the biological function of two of the predicted CLE signaling peptides in the legume Medicago truncatula. These peptides inhibit the activity of the root apical and lateral root meristems in a manner consistent with our functional predictions based on other CLE signaling peptides clustering in the same groups. CONCLUSION: Our analysis provides an identification and classification of a large number of novel potential CLE signaling peptides. The additional motifs we found could lead to future discovery of recognition sites for processing peptidases as well as predictions for receptor binding specificity.
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spelling pubmed-22546192008-02-27 Bioinformatic analysis of the CLE signaling peptide family Oelkers, Karsten Goffard, Nicolas Weiller, Georg F Gresshoff, Peter M Mathesius, Ulrike Frickey, Tancred BMC Plant Biol Research Article BACKGROUND: Plants encode a large number of leucine-rich repeat receptor-like kinases. Legumes encode several LRR-RLK linked to the process of root nodule formation, the ligands of which are unknown. To identify ligands for these receptors, we used a combination of profile hidden Markov models and position-specific iterative BLAST, allowing us to detect new members of the CLV3/ESR (CLE) protein family from publicly available sequence databases. RESULTS: We identified 114 new members of the CLE protein family from various plant species, as well as five protein sequences containing multiple CLE domains. We were able to cluster the CLE domain proteins into 13 distinct groups based on their pairwise similarities in the primary CLE motif. In addition, we identified secondary motifs that coincide with our sequence clusters. The groupings based on the CLE motifs correlate with known biological functions of CLE signaling peptides and are analogous to groupings based on phylogenetic analysis and ectopic overexpression studies. We tested the biological function of two of the predicted CLE signaling peptides in the legume Medicago truncatula. These peptides inhibit the activity of the root apical and lateral root meristems in a manner consistent with our functional predictions based on other CLE signaling peptides clustering in the same groups. CONCLUSION: Our analysis provides an identification and classification of a large number of novel potential CLE signaling peptides. The additional motifs we found could lead to future discovery of recognition sites for processing peptidases as well as predictions for receptor binding specificity. BioMed Central 2008-01-03 /pmc/articles/PMC2254619/ /pubmed/18171480 http://dx.doi.org/10.1186/1471-2229-8-1 Text en Copyright © 2008 Oelkers et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oelkers, Karsten
Goffard, Nicolas
Weiller, Georg F
Gresshoff, Peter M
Mathesius, Ulrike
Frickey, Tancred
Bioinformatic analysis of the CLE signaling peptide family
title Bioinformatic analysis of the CLE signaling peptide family
title_full Bioinformatic analysis of the CLE signaling peptide family
title_fullStr Bioinformatic analysis of the CLE signaling peptide family
title_full_unstemmed Bioinformatic analysis of the CLE signaling peptide family
title_short Bioinformatic analysis of the CLE signaling peptide family
title_sort bioinformatic analysis of the cle signaling peptide family
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254619/
https://www.ncbi.nlm.nih.gov/pubmed/18171480
http://dx.doi.org/10.1186/1471-2229-8-1
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