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Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors
Leukocyte immunoglobulin-like receptors (LILR) are cell surface molecules that regulate the activities of myelomonocytic cells through the balance of inhibitory and activation signals. LILR genes are located within the leukocyte receptor complex (LRC) on chromosome 19q13.4 adjacent to KIR genes, whi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894450/ https://www.ncbi.nlm.nih.gov/pubmed/24257760 http://dx.doi.org/10.1007/s00251-013-0742-5 |
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author | López-Álvarez, María R. Jones, Des C. Jiang, Wei Traherne, James A. Trowsdale, John |
author_facet | López-Álvarez, María R. Jones, Des C. Jiang, Wei Traherne, James A. Trowsdale, John |
author_sort | López-Álvarez, María R. |
collection | PubMed |
description | Leukocyte immunoglobulin-like receptors (LILR) are cell surface molecules that regulate the activities of myelomonocytic cells through the balance of inhibitory and activation signals. LILR genes are located within the leukocyte receptor complex (LRC) on chromosome 19q13.4 adjacent to KIR genes, which are subject to allelic and copy number variation (CNV). LILRB3 (ILT5) and LILRA6 (ILT8) are highly polymorphic receptors with similar extracellular domains. LILRB3 contains inhibitory ITIM motifs and LILRA6 is coupled to an adaptor with activating ITAM motifs. We analysed the sequences of the extracellular immunoglobulin domain-encoding regions of LILRB3 and LILRA6 in 20 individuals, and determined the copy number of these receptors, in addition to those of other members of the LILR family. We found 41 polymorphic sites within the extracellular domains of LILRB3 and LILRA6. Twenty-four of these sites were common to both receptors. LILRA6, but not LILRB3, exhibited CNV. In 20 out of 48 human cell lines from the International Histocompatibility Working Group, LILRA6 was deleted or duplicated. The only other LILR gene exhibiting genomic aberration was LILRA3, in this case due to a partial deletion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00251-013-0742-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3894450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-38944502014-01-22 Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors López-Álvarez, María R. Jones, Des C. Jiang, Wei Traherne, James A. Trowsdale, John Immunogenetics Original Paper Leukocyte immunoglobulin-like receptors (LILR) are cell surface molecules that regulate the activities of myelomonocytic cells through the balance of inhibitory and activation signals. LILR genes are located within the leukocyte receptor complex (LRC) on chromosome 19q13.4 adjacent to KIR genes, which are subject to allelic and copy number variation (CNV). LILRB3 (ILT5) and LILRA6 (ILT8) are highly polymorphic receptors with similar extracellular domains. LILRB3 contains inhibitory ITIM motifs and LILRA6 is coupled to an adaptor with activating ITAM motifs. We analysed the sequences of the extracellular immunoglobulin domain-encoding regions of LILRB3 and LILRA6 in 20 individuals, and determined the copy number of these receptors, in addition to those of other members of the LILR family. We found 41 polymorphic sites within the extracellular domains of LILRB3 and LILRA6. Twenty-four of these sites were common to both receptors. LILRA6, but not LILRB3, exhibited CNV. In 20 out of 48 human cell lines from the International Histocompatibility Working Group, LILRA6 was deleted or duplicated. The only other LILR gene exhibiting genomic aberration was LILRA3, in this case due to a partial deletion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00251-013-0742-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-11-21 2014 /pmc/articles/PMC3894450/ /pubmed/24257760 http://dx.doi.org/10.1007/s00251-013-0742-5 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper López-Álvarez, María R. Jones, Des C. Jiang, Wei Traherne, James A. Trowsdale, John Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title | Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title_full | Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title_fullStr | Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title_full_unstemmed | Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title_short | Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors |
title_sort | copy number and nucleotide variation of the lilr family of myelomonocytic cell activating and inhibitory receptors |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894450/ https://www.ncbi.nlm.nih.gov/pubmed/24257760 http://dx.doi.org/10.1007/s00251-013-0742-5 |
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