The scavenging capacity of DMBT1 is impaired by germline deletions

Open Access
Authors
Publication date 06-2017
Journal Immunogenetics
Volume | Issue number 69 | 6
Pages (from-to) 401-407
Organisations
  • Faculty of Dentistry (ACTA)
Abstract

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.

Document type Article
Language English
Published at https://doi.org/10.1007/s00251-017-0982-x
Other links https://www.scopus.com/pages/publications/85016449435
Downloads
10.1007_s00251-017-0982-x (Final published version)
Permalink to this page
Back