Identification of a novel conserved signaling motif in CD200 receptor required for its inhibitory function

The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein families and are mostly known to mediate protein trafficking between subcellular locations rather than signaling. Therefore, we investigated whe...

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Published inPloS one Vol. 16; no. 3; p. e0244770
Main Authors Timmerman, Laura M, de Graaf, J Fréderique, Satravelas, Nikolaos, Kesmir, Çan, Meyaard, Linde, van der Vlist, Michiel
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 29.03.2021
Public Library of Science (PLoS)
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Abstract The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein families and are mostly known to mediate protein trafficking between subcellular locations rather than signaling. Therefore, we investigated whether additional motifs specify the inhibitory function of CD200R. We performed phylogenetic analysis of the intracellular domain of CD200R in mammals, birds, bony fish, amphibians and reptiles. Indeed, the tyrosine of the NPxY-motif is fully conserved across species, in line with its central role in CD200R signaling. In contrast, P295 of the NPxY-motif is not conserved. Instead, a conserved stretch of negatively charged amino acids, EEDE279, and two conserved residues P285 and K292 in the flanking region prior to the NPxY-motif are required for CD200R mediated inhibition of p-Erk, p-Akt308, p-Akt473, p-rpS6 and LPS-induced IL-8 secretion. Altogether, we show that instead of the more common NPxY-motif, CD200R signaling can be assigned to a unique signaling motif in mammals defined by: EEDExxPYxxYxxKxNxxY.
AbstractList The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein families and are mostly known to mediate protein trafficking between subcellular locations rather than signaling. Therefore, we investigated whether additional motifs specify the inhibitory function of CD200R. We performed phylogenetic analysis of the intracellular domain of CD200R in mammals, birds, bony fish, amphibians and reptiles. Indeed, the tyrosine of the NPxY-motif is fully conserved across species, in line with its central role in CD200R signaling. In contrast, P295 of the NPxY-motif is not conserved. Instead, a conserved stretch of negatively charged amino acids, EEDE279, and two conserved residues P285 and K292 in the flanking region prior to the NPxY-motif are required for CD200R mediated inhibition of p-Erk, p-Akt308, p-Akt473, p-rpS6 and LPS-induced IL-8 secretion. Altogether, we show that instead of the more common NPxY-motif, CD200R signaling can be assigned to a unique signaling motif in mammals defined by: EEDExxPYxxYxxKxNxxY.
CD200R signaling is shown to suppress anti-tumor immunity [8–16], and CD200R expression and function is altered in autoimmunity [17]. Besides autoimmunity and cancer, CD200R is implicated in both viral and bacterial immunity. In mouse hepatitis coronavirus, CD200R inhibits TLR7 signaling, dampening type I IFN production in response to TLR7 ligands [18], and in mouse influenza CD200R decreases inflammation during pulmonary infection [19]. [...]CD200R limits colonisation and proliferation of the bacterium Francisella tularensis by mediating the production of reactive oxygen species in neutrophils [20]. Here, we hypothesize that additional motifs or residues in the intracellular tail of the CD200R are required to exert the full inhibitory function of the CD200R. [...]we assessed conservation of the CD200R signaling domain by sequence analysis in five animal classes and functionally determined the contribution of conserved residues to CD200R signaling. For the phylogenetic analysis all sequences with an annotation “partial” were “low quality” discarded. [...]for every species we took only one isoform of CD200R sequences.
CD200R signaling is shown to suppress anti-tumor immunity [8–16], and CD200R expression and function is altered in autoimmunity [17]. Besides autoimmunity and cancer, CD200R is implicated in both viral and bacterial immunity. In mouse hepatitis coronavirus, CD200R inhibits TLR7 signaling, dampening type I IFN production in response to TLR7 ligands [18], and in mouse influenza CD200R decreases inflammation during pulmonary infection [19]. [...]CD200R limits colonisation and proliferation of the bacterium Francisella tularensis by mediating the production of reactive oxygen species in neutrophils [20]. Here, we hypothesize that additional motifs or residues in the intracellular tail of the CD200R are required to exert the full inhibitory function of the CD200R. [...]we assessed conservation of the CD200R signaling domain by sequence analysis in five animal classes and functionally determined the contribution of conserved residues to CD200R signaling. For the phylogenetic analysis all sequences with an annotation “partial” were “low quality” discarded. [...]for every species we took only one isoform of CD200R sequences.
Audience Academic
Author Satravelas, Nikolaos
Timmerman, Laura M
de Graaf, J Fréderique
Meyaard, Linde
van der Vlist, Michiel
Kesmir, Çan
AuthorAffiliation 2 Oncode Institute, Utrecht, The Netherlands
3 Theoretical Biology & Bioinformatics, Science Faculty, Utrecht University, Utrecht, The Netherlands
1 Department of Immunology, Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands
Baylor University, UNITED STATES
AuthorAffiliation_xml – name: 2 Oncode Institute, Utrecht, The Netherlands
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– name: 3 Theoretical Biology & Bioinformatics, Science Faculty, Utrecht University, Utrecht, The Netherlands
– name: Baylor University, UNITED STATES
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CitedBy_id crossref_primary_10_1016_j_molimm_2022_02_019
crossref_primary_10_1111_all_15850
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2021 Timmerman et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2021 Timmerman et al 2021 Timmerman et al
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– notice: 2021 Timmerman et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2021 Timmerman et al 2021 Timmerman et al
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Snippet The inhibitory signaling of CD200 receptor 1 (CD200R) has been attributed to its NPxY signaling motif. However, NPxY-motifs are present in multiple protein...
CD200R signaling is shown to suppress anti-tumor immunity [8–16], and CD200R expression and function is altered in autoimmunity [17]. Besides autoimmunity and...
CD200R signaling is shown to suppress anti-tumor immunity [8–16], and CD200R expression and function is altered in autoimmunity [17]. Besides autoimmunity and...
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StartPage e0244770
SubjectTerms Annotations
Autoimmunity
Bioinformatics
Biology and Life Sciences
CD200 antigen
Colonization
Computer and Information Sciences
Conservation
Conserved sequence
Coronaviruses
Genetic aspects
Glycoproteins
Hepatitis
Immunity
Immunology
Influenza
Interferon
Leukocytes (neutrophilic)
Ligands
Mutagenesis
Oxygen
Phosphorylation
Phylogenetics
Phylogeny
Proteins
Reactive oxygen species
Research and Analysis Methods
Residues
Sequence analysis
Signaling
Software
Supervision
TLR7 protein
Toll-like receptors
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Title Identification of a novel conserved signaling motif in CD200 receptor required for its inhibitory function
URI https://www.ncbi.nlm.nih.gov/pubmed/33780466
https://www.proquest.com/docview/2506725452
https://search.proquest.com/docview/2507147699
https://pubmed.ncbi.nlm.nih.gov/PMC8007030
https://doaj.org/article/257802a4069840bd93957d84e365c2ab
http://dx.doi.org/10.1371/journal.pone.0244770
Volume 16
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