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Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration
Human genetic factors predispose to tuberculosis (TB). We studied 7.6 million genetic variants in 5,530 pulmonary TB patients and 5,607 healthy controls. In the combined analysis of these subjects and the follow-up cohort (15,087 TB patients and controls altogether), we found association between TB...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414475/ https://www.ncbi.nlm.nih.gov/pubmed/25774636 http://dx.doi.org/10.1038/ng.3248 |
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author | Curtis, James Luo, Yang Zenner, Helen L. Cuchet-Lourenço, Delphine Wu, Changxin Lo, Kitty Maes, Mailis Alisaac, Ali Stebbings, Emma Liu, Jimmy Z. Kopanitsa, Liliya Ignatyeva, Olga Balabanova, Yanina Nikolayevskyy, Vladyslav Baessmann, Ingelore Thye, Thorsten Meyer, Christian G. Nürnberg, Peter Horstmann, Rolf D. Drobniewski, Francis Plagnol, Vincent Barrett, Jeffrey C. Nejentsev, Sergey |
author_facet | Curtis, James Luo, Yang Zenner, Helen L. Cuchet-Lourenço, Delphine Wu, Changxin Lo, Kitty Maes, Mailis Alisaac, Ali Stebbings, Emma Liu, Jimmy Z. Kopanitsa, Liliya Ignatyeva, Olga Balabanova, Yanina Nikolayevskyy, Vladyslav Baessmann, Ingelore Thye, Thorsten Meyer, Christian G. Nürnberg, Peter Horstmann, Rolf D. Drobniewski, Francis Plagnol, Vincent Barrett, Jeffrey C. Nejentsev, Sergey |
author_sort | Curtis, James |
collection | PubMed |
description | Human genetic factors predispose to tuberculosis (TB). We studied 7.6 million genetic variants in 5,530 pulmonary TB patients and 5,607 healthy controls. In the combined analysis of these subjects and the follow-up cohort (15,087 TB patients and controls altogether), we found association between TB and variants located in introns of the ASAP1 gene on chromosome 8q24 (P = 2.6 × 10(−11) for rs4733781; P = 1.0 × 10(−10) for rs10956514). Dendritic cells (DCs) showed high level of ASAP1 expression, which was reduced after M. tuberculosis infection, and rs10956514 was associated with the level of reduction of ASAP1 expression. The ASAP1 protein is involved in actin and membrane remodeling and has been associated with podosomes. The ASAP1-depleted DCs showed impaired matrix degradation and migration. Therefore, genetically determined excessive reduction of ASAP1 expression in M. tuberculosis-infected DCs may lead to their impaired migration, suggesting a potential novel mechanism that predisposes to TB. |
format | Online Article Text |
id | pubmed-4414475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-44144752015-11-01 Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration Curtis, James Luo, Yang Zenner, Helen L. Cuchet-Lourenço, Delphine Wu, Changxin Lo, Kitty Maes, Mailis Alisaac, Ali Stebbings, Emma Liu, Jimmy Z. Kopanitsa, Liliya Ignatyeva, Olga Balabanova, Yanina Nikolayevskyy, Vladyslav Baessmann, Ingelore Thye, Thorsten Meyer, Christian G. Nürnberg, Peter Horstmann, Rolf D. Drobniewski, Francis Plagnol, Vincent Barrett, Jeffrey C. Nejentsev, Sergey Nat Genet Article Human genetic factors predispose to tuberculosis (TB). We studied 7.6 million genetic variants in 5,530 pulmonary TB patients and 5,607 healthy controls. In the combined analysis of these subjects and the follow-up cohort (15,087 TB patients and controls altogether), we found association between TB and variants located in introns of the ASAP1 gene on chromosome 8q24 (P = 2.6 × 10(−11) for rs4733781; P = 1.0 × 10(−10) for rs10956514). Dendritic cells (DCs) showed high level of ASAP1 expression, which was reduced after M. tuberculosis infection, and rs10956514 was associated with the level of reduction of ASAP1 expression. The ASAP1 protein is involved in actin and membrane remodeling and has been associated with podosomes. The ASAP1-depleted DCs showed impaired matrix degradation and migration. Therefore, genetically determined excessive reduction of ASAP1 expression in M. tuberculosis-infected DCs may lead to their impaired migration, suggesting a potential novel mechanism that predisposes to TB. 2015-03-16 2015-05 /pmc/articles/PMC4414475/ /pubmed/25774636 http://dx.doi.org/10.1038/ng.3248 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Curtis, James Luo, Yang Zenner, Helen L. Cuchet-Lourenço, Delphine Wu, Changxin Lo, Kitty Maes, Mailis Alisaac, Ali Stebbings, Emma Liu, Jimmy Z. Kopanitsa, Liliya Ignatyeva, Olga Balabanova, Yanina Nikolayevskyy, Vladyslav Baessmann, Ingelore Thye, Thorsten Meyer, Christian G. Nürnberg, Peter Horstmann, Rolf D. Drobniewski, Francis Plagnol, Vincent Barrett, Jeffrey C. Nejentsev, Sergey Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title | Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title_full | Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title_fullStr | Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title_full_unstemmed | Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title_short | Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration |
title_sort | susceptibility to tuberculosis is associated with variants in the asap1 gene encoding a regulator of dendritic cell migration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414475/ https://www.ncbi.nlm.nih.gov/pubmed/25774636 http://dx.doi.org/10.1038/ng.3248 |
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