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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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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. |
format | Online Article Text |
id | pubmed-5435793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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