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Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population

HLA-Cw6 is one of the most associated alleles in psoriasis. Recently, Late Cornified Envelop 3 (LCE3) genes were identified as a susceptibility factor for psoriasis. Some population showed epistatic interaction of LCE3 risk variants with HLA-Cw6, while some population failed to show any association....

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Autores principales: Chandra, Aditi, Lahiri, Anirudhya, Senapati, Swapan, Basu, Baidehi, Ghosh, Saurabh, Mukhopadhyay, Indranil, Behra, Akhilesh, Sarkar, Somenath, Chatterjee, Gobinda, Chatterjee, Raghunath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822143/
https://www.ncbi.nlm.nih.gov/pubmed/27048876
http://dx.doi.org/10.1038/srep24059
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author Chandra, Aditi
Lahiri, Anirudhya
Senapati, Swapan
Basu, Baidehi
Ghosh, Saurabh
Mukhopadhyay, Indranil
Behra, Akhilesh
Sarkar, Somenath
Chatterjee, Gobinda
Chatterjee, Raghunath
author_facet Chandra, Aditi
Lahiri, Anirudhya
Senapati, Swapan
Basu, Baidehi
Ghosh, Saurabh
Mukhopadhyay, Indranil
Behra, Akhilesh
Sarkar, Somenath
Chatterjee, Gobinda
Chatterjee, Raghunath
author_sort Chandra, Aditi
collection PubMed
description HLA-Cw6 is one of the most associated alleles in psoriasis. Recently, Late Cornified Envelop 3 (LCE3) genes were identified as a susceptibility factor for psoriasis. Some population showed epistatic interaction of LCE3 risk variants with HLA-Cw6, while some population failed to show any association. We determined the associations of a 32.2 kb deletion comprising LCE3C-3B genes and three SNPs (rs1886734, rs4112788; rs7516108) at the LCE3 gene cluster among the psoriasis patients in India. All three SNPs at the LCE3 gene cluster failed to show any association. In contrary, for patients with HLA-Cw6 allele, all three SNPs and the LCE3C-3B deletion showed significant associations. While, all five LCE3 genes were upregulated in psoriatic skin, only LCE3A showed significant overexpression with homozygous risk genotype compared to the non-risk genotype. LCE3B also showed significant overexpression in patients with HLA-Cw6 allele. Moreover, LCE3A showed significantly higher expression in patients bearing homozygous risk genotype in presence of HLA-Cw6 allele but not in those having non-risk genotype, demonstrating the combined effect of HLA-Cw6 allele and risk associated genotype near LCE3A gene. Integration of genetic and gene expression data thus allowed us to identify the actual disease variants at the LCE3 cluster among the psoriasis patients in India.
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spelling pubmed-48221432016-04-18 Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population Chandra, Aditi Lahiri, Anirudhya Senapati, Swapan Basu, Baidehi Ghosh, Saurabh Mukhopadhyay, Indranil Behra, Akhilesh Sarkar, Somenath Chatterjee, Gobinda Chatterjee, Raghunath Sci Rep Article HLA-Cw6 is one of the most associated alleles in psoriasis. Recently, Late Cornified Envelop 3 (LCE3) genes were identified as a susceptibility factor for psoriasis. Some population showed epistatic interaction of LCE3 risk variants with HLA-Cw6, while some population failed to show any association. We determined the associations of a 32.2 kb deletion comprising LCE3C-3B genes and three SNPs (rs1886734, rs4112788; rs7516108) at the LCE3 gene cluster among the psoriasis patients in India. All three SNPs at the LCE3 gene cluster failed to show any association. In contrary, for patients with HLA-Cw6 allele, all three SNPs and the LCE3C-3B deletion showed significant associations. While, all five LCE3 genes were upregulated in psoriatic skin, only LCE3A showed significant overexpression with homozygous risk genotype compared to the non-risk genotype. LCE3B also showed significant overexpression in patients with HLA-Cw6 allele. Moreover, LCE3A showed significantly higher expression in patients bearing homozygous risk genotype in presence of HLA-Cw6 allele but not in those having non-risk genotype, demonstrating the combined effect of HLA-Cw6 allele and risk associated genotype near LCE3A gene. Integration of genetic and gene expression data thus allowed us to identify the actual disease variants at the LCE3 cluster among the psoriasis patients in India. Nature Publishing Group 2016-04-06 /pmc/articles/PMC4822143/ /pubmed/27048876 http://dx.doi.org/10.1038/srep24059 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chandra, Aditi
Lahiri, Anirudhya
Senapati, Swapan
Basu, Baidehi
Ghosh, Saurabh
Mukhopadhyay, Indranil
Behra, Akhilesh
Sarkar, Somenath
Chatterjee, Gobinda
Chatterjee, Raghunath
Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title_full Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title_fullStr Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title_full_unstemmed Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title_short Increased Risk of Psoriasis due to combined effect of HLA-Cw6 and LCE3 risk alleles in Indian population
title_sort increased risk of psoriasis due to combined effect of hla-cw6 and lce3 risk alleles in indian population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822143/
https://www.ncbi.nlm.nih.gov/pubmed/27048876
http://dx.doi.org/10.1038/srep24059
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