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The scavenging capacity of DMBT1 is impaired by germline deletions

The Scavenger Receptor Cysteine-Rich (SRCR) proteins are an archaic group of proteins characterized by the presence of multiple SRCR domains. They are membrane-bound or secreted proteins, which are generally related to host defense systems in animals. Deleted in Malignant Brain Tumors 1 (DMBT1) is a...

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Autores principales: Bikker, Floris J., End, Caroline, Ligtenberg, Antoon J. M., Blaich, Stephanie, Lyer, Stefan, Renner, Marcus, Wittig, Rainer, Nazmi, Kamran, van Nieuw Amerongen, Arie, Poustka, Annemarie, Veerman, Enno C.I., Mollenhauer, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435793/
https://www.ncbi.nlm.nih.gov/pubmed/28364129
http://dx.doi.org/10.1007/s00251-017-0982-x
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author Bikker, Floris J.
End, Caroline
Ligtenberg, Antoon J. M.
Blaich, Stephanie
Lyer, Stefan
Renner, Marcus
Wittig, Rainer
Nazmi, Kamran
van Nieuw Amerongen, Arie
Poustka, Annemarie
Veerman, Enno C.I.
Mollenhauer, Jan
author_facet Bikker, Floris J.
End, Caroline
Ligtenberg, Antoon J. M.
Blaich, Stephanie
Lyer, Stefan
Renner, Marcus
Wittig, Rainer
Nazmi, Kamran
van Nieuw Amerongen, Arie
Poustka, Annemarie
Veerman, Enno C.I.
Mollenhauer, Jan
author_sort Bikker, Floris J.
collection PubMed
description The Scavenger Receptor Cysteine-Rich (SRCR) proteins are an archaic group of proteins characterized by the presence of multiple SRCR domains. They are membrane-bound or secreted proteins, which are generally related to host defense systems in animals. Deleted in Malignant Brain Tumors 1 (DMBT1) is a SRCR protein which is secreted in mucosal fluids and involved in host defense by pathogen binding by its SRCR domains. Genetic polymorphism within DMBT1 leads to DMBT1-alleles giving rise to polypeptides with interindividually different numbers of SRCR domains, ranging from 8 SRCR domains (encoded by 6 kb DMBT1 variant) to 13 SRCR domains (encoded by the 8 kb DMBT1 variant). In the present study, we have investigated whether reduction from 13 to 8 amino-terminal SRCR domains leads to reduction of bacterial binding. The 6 kb variant bound ~20–45% less bacteria compared to the 8 kb variant. These results support the hypothesis that genetic variation in DMBT1 may influence microbial defense.
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spelling pubmed-54357932017-05-31 The scavenging capacity of DMBT1 is impaired by germline deletions Bikker, Floris J. End, Caroline Ligtenberg, Antoon J. M. Blaich, Stephanie Lyer, Stefan Renner, Marcus Wittig, Rainer Nazmi, Kamran van Nieuw Amerongen, Arie Poustka, Annemarie Veerman, Enno C.I. Mollenhauer, Jan Immunogenetics Short Communication The Scavenger Receptor Cysteine-Rich (SRCR) proteins are an archaic group of proteins characterized by the presence of multiple SRCR domains. They are membrane-bound or secreted proteins, which are generally related to host defense systems in animals. Deleted in Malignant Brain Tumors 1 (DMBT1) is a SRCR protein which is secreted in mucosal fluids and involved in host defense by pathogen binding by its SRCR domains. Genetic polymorphism within DMBT1 leads to DMBT1-alleles giving rise to polypeptides with interindividually different numbers of SRCR domains, ranging from 8 SRCR domains (encoded by 6 kb DMBT1 variant) to 13 SRCR domains (encoded by the 8 kb DMBT1 variant). In the present study, we have investigated whether reduction from 13 to 8 amino-terminal SRCR domains leads to reduction of bacterial binding. The 6 kb variant bound ~20–45% less bacteria compared to the 8 kb variant. These results support the hypothesis that genetic variation in DMBT1 may influence microbial defense. Springer Berlin Heidelberg 2017-03-31 2017 /pmc/articles/PMC5435793/ /pubmed/28364129 http://dx.doi.org/10.1007/s00251-017-0982-x Text en © The Author(s) 2017 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 Short Communication
Bikker, Floris J.
End, Caroline
Ligtenberg, Antoon J. M.
Blaich, Stephanie
Lyer, Stefan
Renner, Marcus
Wittig, Rainer
Nazmi, Kamran
van Nieuw Amerongen, Arie
Poustka, Annemarie
Veerman, Enno C.I.
Mollenhauer, Jan
The scavenging capacity of DMBT1 is impaired by germline deletions
title The scavenging capacity of DMBT1 is impaired by germline deletions
title_full The scavenging capacity of DMBT1 is impaired by germline deletions
title_fullStr The scavenging capacity of DMBT1 is impaired by germline deletions
title_full_unstemmed The scavenging capacity of DMBT1 is impaired by germline deletions
title_short The scavenging capacity of DMBT1 is impaired by germline deletions
title_sort scavenging capacity of dmbt1 is impaired by germline deletions
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435793/
https://www.ncbi.nlm.nih.gov/pubmed/28364129
http://dx.doi.org/10.1007/s00251-017-0982-x
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