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The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family

The leukocyte receptor complex (LRC) encodes numerous immunoglobulin (Ig)-like receptors involved in innate immunity. These include the killer-cell Ig-like receptors (KIR) and the leukocyte Ig-like receptors (LILR) which can be polymorphic and vary greatly in number between species. Using the recent...

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Autores principales: Schwartz, John C., Hammond, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182393/
https://www.ncbi.nlm.nih.gov/pubmed/29931472
http://dx.doi.org/10.1007/s00251-018-1067-1
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author Schwartz, John C.
Hammond, John A.
author_facet Schwartz, John C.
Hammond, John A.
author_sort Schwartz, John C.
collection PubMed
description The leukocyte receptor complex (LRC) encodes numerous immunoglobulin (Ig)-like receptors involved in innate immunity. These include the killer-cell Ig-like receptors (KIR) and the leukocyte Ig-like receptors (LILR) which can be polymorphic and vary greatly in number between species. Using the recent long-read genome assembly, Sscrofa11.1, we have characterized the porcine LRC on chromosome 6. We identified a ~ 197-kb region containing numerous LILR genes that were missing in previous assemblies. Out of 17 such LILR genes and fragments, six encode functional proteins, of which three are inhibitory and three are activating, while the majority of pseudogenes had the potential to encode activating receptors. Elsewhere in the LRC, between FCAR and GP6, we identified a novel gene that encodes two Ig-like domains and a long inhibitory intracellular tail. Comparison with two other porcine assemblies revealed a second, nearly identical, non-functional gene encoding a short intracellular tail with ambiguous function. These novel genes were found in a diverse range of mammalian species, including a pseudogene in humans, and typically consist of a single long-tailed receptor and a variable number of short-tailed receptors. Using porcine transcriptome data, both the novel inhibitory gene and the LILR were highly expressed in peripheral blood, while the single KIR gene, KIR2DL1, was either very poorly expressed or not at all. These observations are a prerequisite for improved understanding of immune cell functions in the pig and other species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00251-018-1067-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-61823932018-10-22 The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family Schwartz, John C. Hammond, John A. Immunogenetics Original Article The leukocyte receptor complex (LRC) encodes numerous immunoglobulin (Ig)-like receptors involved in innate immunity. These include the killer-cell Ig-like receptors (KIR) and the leukocyte Ig-like receptors (LILR) which can be polymorphic and vary greatly in number between species. Using the recent long-read genome assembly, Sscrofa11.1, we have characterized the porcine LRC on chromosome 6. We identified a ~ 197-kb region containing numerous LILR genes that were missing in previous assemblies. Out of 17 such LILR genes and fragments, six encode functional proteins, of which three are inhibitory and three are activating, while the majority of pseudogenes had the potential to encode activating receptors. Elsewhere in the LRC, between FCAR and GP6, we identified a novel gene that encodes two Ig-like domains and a long inhibitory intracellular tail. Comparison with two other porcine assemblies revealed a second, nearly identical, non-functional gene encoding a short intracellular tail with ambiguous function. These novel genes were found in a diverse range of mammalian species, including a pseudogene in humans, and typically consist of a single long-tailed receptor and a variable number of short-tailed receptors. Using porcine transcriptome data, both the novel inhibitory gene and the LILR were highly expressed in peripheral blood, while the single KIR gene, KIR2DL1, was either very poorly expressed or not at all. These observations are a prerequisite for improved understanding of immune cell functions in the pig and other species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00251-018-1067-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-06-21 2018 /pmc/articles/PMC6182393/ /pubmed/29931472 http://dx.doi.org/10.1007/s00251-018-1067-1 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Schwartz, John C.
Hammond, John A.
The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title_full The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title_fullStr The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title_full_unstemmed The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title_short The unique evolution of the pig LRC, a single KIR but expansion of LILR and a novel Ig receptor family
title_sort unique evolution of the pig lrc, a single kir but expansion of lilr and a novel ig receptor family
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182393/
https://www.ncbi.nlm.nih.gov/pubmed/29931472
http://dx.doi.org/10.1007/s00251-018-1067-1
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