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 in | PloS one Vol. 16; no. 3; p. e0244770 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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29.03.2021
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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. |
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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 – name: 1 Department of Immunology, Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands – name: 3 Theoretical Biology & Bioinformatics, Science Faculty, Utrecht University, Utrecht, The Netherlands – name: Baylor University, UNITED STATES |
Author_xml | – sequence: 1 givenname: Laura M orcidid: 0000-0002-2848-1681 surname: Timmerman fullname: Timmerman, Laura M organization: Oncode Institute, Utrecht, The Netherlands – sequence: 2 givenname: J Fréderique surname: de Graaf fullname: de Graaf, J Fréderique organization: Department of Immunology, Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands – sequence: 3 givenname: Nikolaos surname: Satravelas fullname: Satravelas, Nikolaos organization: Theoretical Biology & Bioinformatics, Science Faculty, Utrecht University, Utrecht, The Netherlands – sequence: 4 givenname: Çan surname: Kesmir fullname: Kesmir, Çan organization: Theoretical Biology & Bioinformatics, Science Faculty, Utrecht University, Utrecht, The Netherlands – sequence: 5 givenname: Linde surname: Meyaard fullname: Meyaard, Linde organization: Oncode Institute, Utrecht, The Netherlands – sequence: 6 givenname: Michiel surname: van der Vlist fullname: van der Vlist, Michiel organization: Oncode Institute, Utrecht, The Netherlands |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33780466$$D View this record in MEDLINE/PubMed |
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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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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 |
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