The scavenging capacity of DMBT1 is impaired by germline deletions
| Authors |
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| Publication date | 06-2017 |
| Journal | Immunogenetics |
| Volume | Issue number | 69 | 6 |
| Pages (from-to) | 401-407 |
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| 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
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