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Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy
Leprosy has long been thought to have a strong genetic component, and so far, only positional cloning and genomewide association studies have been used to study the genetic susceptibility to leprosy,while whole exome sequencing (WES) approach has not yet been applied. In this study, we used WES appr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703986/ https://www.ncbi.nlm.nih.gov/pubmed/29180661 http://dx.doi.org/10.1038/s41598-017-16422-1 |
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author | Yuan, Youhua You, Yuangang Wen, Yan Liu, Jian Li, Huanying Zhang, Yumeng Wu, Nan Liu, Shuang Zhang, Shanshan Chen, Jiazhen Ai, Jingwen Zhang, Wenhong Zhang, Ying |
author_facet | Yuan, Youhua You, Yuangang Wen, Yan Liu, Jian Li, Huanying Zhang, Yumeng Wu, Nan Liu, Shuang Zhang, Shanshan Chen, Jiazhen Ai, Jingwen Zhang, Wenhong Zhang, Ying |
author_sort | Yuan, Youhua |
collection | PubMed |
description | Leprosy has long been thought to have a strong genetic component, and so far, only positional cloning and genomewide association studies have been used to study the genetic susceptibility to leprosy,while whole exome sequencing (WES) approach has not yet been applied. In this study, we used WES approach on four leprosy patients and four healthy control relatives from two leprosy families. We found three new susceptible loci of leprosy, one in GAL3ST4 and two in CHGB. We went on to validate the findings of WES using 151 leprosy cases and 226 healthy controls by Sanger sequencing. Stratified by gender, GAL3ST4 was found to be the susceptible gene only for the female population, and CHGB48 and CHGB23 were susceptibile to leprosy for the male population, respectively). Moreover, the gene expression levels of the three susceptible loci were measured by real-time PCR after the stimulation by M. leprae antigens in the PBMC (peripheral blood mononuclear cells) of 69 healthy people. The results showed that the female subjects with high frequent genotype in GAL3ST4 had a fivefold elevated expression. We suggest the polymorphisms in GAL3ST4 in different population are associated with increased risk of leprosy. |
format | Online Article Text |
id | pubmed-5703986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57039862017-11-30 Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy Yuan, Youhua You, Yuangang Wen, Yan Liu, Jian Li, Huanying Zhang, Yumeng Wu, Nan Liu, Shuang Zhang, Shanshan Chen, Jiazhen Ai, Jingwen Zhang, Wenhong Zhang, Ying Sci Rep Article Leprosy has long been thought to have a strong genetic component, and so far, only positional cloning and genomewide association studies have been used to study the genetic susceptibility to leprosy,while whole exome sequencing (WES) approach has not yet been applied. In this study, we used WES approach on four leprosy patients and four healthy control relatives from two leprosy families. We found three new susceptible loci of leprosy, one in GAL3ST4 and two in CHGB. We went on to validate the findings of WES using 151 leprosy cases and 226 healthy controls by Sanger sequencing. Stratified by gender, GAL3ST4 was found to be the susceptible gene only for the female population, and CHGB48 and CHGB23 were susceptibile to leprosy for the male population, respectively). Moreover, the gene expression levels of the three susceptible loci were measured by real-time PCR after the stimulation by M. leprae antigens in the PBMC (peripheral blood mononuclear cells) of 69 healthy people. The results showed that the female subjects with high frequent genotype in GAL3ST4 had a fivefold elevated expression. We suggest the polymorphisms in GAL3ST4 in different population are associated with increased risk of leprosy. Nature Publishing Group UK 2017-11-27 /pmc/articles/PMC5703986/ /pubmed/29180661 http://dx.doi.org/10.1038/s41598-017-16422-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yuan, Youhua You, Yuangang Wen, Yan Liu, Jian Li, Huanying Zhang, Yumeng Wu, Nan Liu, Shuang Zhang, Shanshan Chen, Jiazhen Ai, Jingwen Zhang, Wenhong Zhang, Ying Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title | Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title_full | Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title_fullStr | Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title_full_unstemmed | Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title_short | Identification of novel genetic loci GAL3ST4 and CHGB involved in susceptibility to leprosy |
title_sort | identification of novel genetic loci gal3st4 and chgb involved in susceptibility to leprosy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703986/ https://www.ncbi.nlm.nih.gov/pubmed/29180661 http://dx.doi.org/10.1038/s41598-017-16422-1 |
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