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The Sequenced Genomes of Non-Flowering Land Plants Reveal the (R)Evolutionary History of Peptide Signaling

https://doi.org/10.1101/2020.06.02.130120

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Insights into Land Plant Evolution Garnered from the Marchantia polymorpha Genome

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Genomes of Subaerial Zygnematophyceae Provide Insights into Land Plant Evolution

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The Penium margaritaceum Genome: Hallmarks of the Origins of Land Plants

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A Novel Pollen-Pistil Interaction Conferring High-Temperature Tolerance during Reproduction via CLE45 Signaling

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CLAVATA Was a Genetic Novelty for the Morphological Innovation of 3D Growth in Land Plants

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Induction of Multichotomous Branching by CLAVATA Peptide in Marchantia polymorpha

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Phosphate Starvation-Dependent Iron Mobilization Induces CLE14 Expression to Trigger Root Meristem Differentiation through CLV2/PEPR2 Signaling

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Lateral Inhibition by a Peptide Hormone-Receptor Cascade during Arabidopsis Lateral Root Founder Cell Formation

inferredcites →https://doi.org/10.1016/j.molp.2016.10.002openalex-snapshot

Structural Insight into Recognition of Plant Peptide Hormones by Receptors

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Walkabout on the long branches of plant evolution

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SERKing Coreceptors for Receptors

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Basic Local Alignment Search Tool

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The CLAVATA1Gene Encodes a Putative Receptor Kinase That Controls Shoot and Floral Meristem Size in Arabidopsis

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ROS1, a Repressor of Transcriptional Gene Silencing in Arabidopsis, Encodes a DNA Glycosylase/Lyase

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Statistical methods for detecting molecular adaptation

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Anthoceros genomes illuminate the origin of land plants and the unique biology of hornworts

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One thousand plant transcriptomes and the phylogenomics of green plants

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Machine learning-guided discovery and design of non-hemolytic peptides

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Identification of tyrosylprotein sulfotransferase in Arabidopsis

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Identification of three LRR-RKs involved in perception of root meristem growth factor in Arabidopsis

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Receptor-like kinases from Arabidopsis form a monophyletic gene family related to animal receptor kinases

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The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

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trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses

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Tanglegrams for rooted phylogenetic trees and networks

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InterProScan 5: genome-scale protein function classification

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Sulfated plant peptide hormones

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MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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Protein sequence similarity searches using patterns as seeds

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MUSCLE: multiple sequence alignment with high accuracy and high throughput

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PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments

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The Arabidopsis Information Resource (TAIR): improved gene annotation and new tools

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SWISS-MODEL: homology modelling of protein structures and complexes

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Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference

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Phytosulfokine Stimulates Somatic Embryogenesis in Cryptomeria japonica

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Mechanisms and Strategies Shaping Plant Peptide Hormones

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WebLogo: A Sequence Logo Generator: Figure 1

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Developmental Evolution of the Sexual Process in Ancient Flowering Plant Lineages

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The EPIP Peptide of INFLORESCENCE DEFICIENT IN ABSCISSION Is Sufficient to Induce Abscission in Arabidopsis through the Receptor-Like Kinases HAESA and HAESA-LIKE2

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Tools and Strategies to Match Peptide-Ligand Receptor Pairs

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GASSHO1 and GASSHO2 encoding a putative leucine‐rich repeat transmembrane‐type receptor kinase are essential for the normal development of the epidermal surface in Arabidopsis embryos

inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00904.xopenalex-snapshot

Regulation of Vascular Development by CLE Peptide‐receptor Systems

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Why we need more non‐seed plant models

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Structural evolution drives diversification of the large LRR‐RLK gene family

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Regulation of plant peptide hormones and growth factors by post‐translational modification

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The Physcomitrella patens chromosome‐scale assembly reveals moss genome structure and evolution

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Leucine‐rich repeat receptor‐like kinase II phylogenetics reveals five main clades throughout the plant kingdom

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Origin and Radiation of the Earliest Vascular Land Plants

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Secreted Peptide Signals Required for Maintenance of Root Stem Cell Niche in Arabidopsis

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The Selaginella Genome Identifies Genetic Changes Associated with the Evolution of Vascular Plants

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The Amborella Genome and the Evolution of Flowering Plants

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Perception of root-derived peptides by shoot LRR-RKs mediates systemic N-demand signaling

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A peptide hormone required for Casparian strip diffusion barrier formation in Arabidopsis roots

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Root diffusion barrier control by a vasculature-derived peptide binding to the SGN3 receptor

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A two-way molecular dialogue between embryo and endosperm is required for seed development

inferredcites →https://doi.org/10.1126/stke.2001.113.re22openalex-snapshot

Plant Receptor-Like Kinase Gene Family: Diversity, Function, and Signaling

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Look Closely, the Beautiful May Be Small: Precursor-Derived Peptides in Plants

inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120122openalex-snapshot

Posttranslationally Modified Small-Peptide Signals in Plants

inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144204openalex-snapshot

PEPTIDE HORMONES IN PLANTS

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The Earliest Land Plants

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Bioinformatic analysis of the CLE signaling peptide family

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Origin and diversification of leucine-rich repeat receptor-like protein kinase (LRR-RLK) genes in plants

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Genome-wide identification and evolutionary analysis of leucine-rich repeat receptor-like protein kinase genes in soybean

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CLAVATA3 is a specific regulator of shoot and floral meristem development affecting the same processes as CLAVATA1

inferredcites →https://doi.org/10.1371/journal.pgen.1007997openalex-snapshot

Control of proliferation in the haploid meristem by CLE peptide signaling in Marchantia polymorpha

inferredcites →https://doi.org/10.1371/journal.pone.0021614openalex-snapshot

LRR Conservation Mapping to Predict Functional Sites within Protein Leucine-Rich Repeat Domains

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FLS2-BAK1 Extracellular Domain Interaction Sites Required for Defense Signaling Activation

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The Secreted Peptide PIP1 Amplifies Immunity through Receptor-Like Kinase 7

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Perception of root‐active CLE peptides requires CORYNE function in the phloem vasculature

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Conservation of the abscission signaling peptide IDA during Angiosperm evolution: withstanding genome duplications and gain and loss of the receptors HAE/HSL2

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Duplication and Divergence of Leucine-Rich Repeat Receptor-Like Protein Kinase (LRR-RLK) Genes in Basal Angiosperm Amborella trichopoda

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The Evolutionarily Conserved Serine Residues in BRI1 LRR Motifs Are Critical for Protein Secretion

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The LRR-RLK Protein HSL3 Regulates Stomatal Closure and the Drought Stress Response by Modulating Hydrogen Peroxide Homeostasis

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inferredcites →https://doi.org/10.3390/plants8070225openalex-snapshot

Control of Organ Abscission and Other Cell Separation Processes by Evolutionary Conserved Peptide Signaling

inferredcites →https://doi.org/10.3390/plants8110520openalex-snapshot

Cunninghamia lanceolata PSK Peptide Hormone Genes Promote Primary Root Growth and Adventitious Root Formation

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1093/jxb/erab233openalex-snapshot

Tyrosylprotein sulfotransferase-dependent and -independent regulation of root development and signaling by PSK LRR receptor kinases in Arabidopsis

inferred← citeshttps://doi.org/10.1111/ppl.14172openalex-snapshot

Land plant peptide signaling: What we know—and don't know—about its evolution

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