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The Turkey Ig-Like Receptor Family: Identification, Expression and Function

The chicken leukocyte receptor complex located on microchromosome 31 encodes the chicken Ig-like receptors (CHIR), a vastly expanded gene family which can be further divided into three subgroups: activating CHIR-A, bifunctional CHIR-AB and inhibitory CHIR-B. Here, we investigated the presence of CHI...

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Autores principales: Windau, Katharina, Viertlboeck, Birgit C., Göbel, Thomas W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601082/
https://www.ncbi.nlm.nih.gov/pubmed/23527222
http://dx.doi.org/10.1371/journal.pone.0059577
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author Windau, Katharina
Viertlboeck, Birgit C.
Göbel, Thomas W.
author_facet Windau, Katharina
Viertlboeck, Birgit C.
Göbel, Thomas W.
author_sort Windau, Katharina
collection PubMed
description The chicken leukocyte receptor complex located on microchromosome 31 encodes the chicken Ig-like receptors (CHIR), a vastly expanded gene family which can be further divided into three subgroups: activating CHIR-A, bifunctional CHIR-AB and inhibitory CHIR-B. Here, we investigated the presence of CHIR homologues in other bird species. The available genome databases of turkey, duck and zebra finch were screened with different strategies including BLAST searches employing various CHIR sequences, and keyword searches. We could not identify CHIR homologues in the distantly related zebra finch and duck, however, several partial and complete sequences of CHIR homologues were identified on chromosome 3 of the turkey genome. They were designated as turkey Ig-like receptors (TILR). Using cDNA derived from turkey blood and spleen RNA, six full length TILR could be amplified and further divided according to the typical sequence features into one activating TILR-A, one inhibitory TILR-B and four bifunctional TILR-AB. Since the TILR-AB sequences all displayed the critical residues shown to be involved in binding to IgY, we next confirmed the IgY binding using a soluble TILR-AB1-huIg fusion protein. This fusion protein reacted with IgY derived from various gallinaceous birds, but not with IgY from other bird species. Finally, we tested various mab directed against CHIR for their crossreactivity with either turkey or duck leukocytes. Whereas no staining was detectable with duck cells, the CHIR-AB1 specific mab 8D12 and the CHIR-A2 specific mab 13E2 both reacted with a leukocyte subpopulation that was further identified as thrombocytes by double immunofluorescence employing B-cell, T-cell and thrombocyte specific reagents. In summary, although the turkey harbors similar LRC genes as the chicken, their distribution seems to be distinct with predominance on thrombocytes rather than lymphocytes.
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spelling pubmed-36010822013-03-22 The Turkey Ig-Like Receptor Family: Identification, Expression and Function Windau, Katharina Viertlboeck, Birgit C. Göbel, Thomas W. PLoS One Research Article The chicken leukocyte receptor complex located on microchromosome 31 encodes the chicken Ig-like receptors (CHIR), a vastly expanded gene family which can be further divided into three subgroups: activating CHIR-A, bifunctional CHIR-AB and inhibitory CHIR-B. Here, we investigated the presence of CHIR homologues in other bird species. The available genome databases of turkey, duck and zebra finch were screened with different strategies including BLAST searches employing various CHIR sequences, and keyword searches. We could not identify CHIR homologues in the distantly related zebra finch and duck, however, several partial and complete sequences of CHIR homologues were identified on chromosome 3 of the turkey genome. They were designated as turkey Ig-like receptors (TILR). Using cDNA derived from turkey blood and spleen RNA, six full length TILR could be amplified and further divided according to the typical sequence features into one activating TILR-A, one inhibitory TILR-B and four bifunctional TILR-AB. Since the TILR-AB sequences all displayed the critical residues shown to be involved in binding to IgY, we next confirmed the IgY binding using a soluble TILR-AB1-huIg fusion protein. This fusion protein reacted with IgY derived from various gallinaceous birds, but not with IgY from other bird species. Finally, we tested various mab directed against CHIR for their crossreactivity with either turkey or duck leukocytes. Whereas no staining was detectable with duck cells, the CHIR-AB1 specific mab 8D12 and the CHIR-A2 specific mab 13E2 both reacted with a leukocyte subpopulation that was further identified as thrombocytes by double immunofluorescence employing B-cell, T-cell and thrombocyte specific reagents. In summary, although the turkey harbors similar LRC genes as the chicken, their distribution seems to be distinct with predominance on thrombocytes rather than lymphocytes. Public Library of Science 2013-03-18 /pmc/articles/PMC3601082/ /pubmed/23527222 http://dx.doi.org/10.1371/journal.pone.0059577 Text en © 2013 Windau et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Windau, Katharina
Viertlboeck, Birgit C.
Göbel, Thomas W.
The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title_full The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title_fullStr The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title_full_unstemmed The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title_short The Turkey Ig-Like Receptor Family: Identification, Expression and Function
title_sort turkey ig-like receptor family: identification, expression and function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601082/
https://www.ncbi.nlm.nih.gov/pubmed/23527222
http://dx.doi.org/10.1371/journal.pone.0059577
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