Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.

<h4>Background</h4>Fc gamma receptors (FcγRs) play a crucial role in immunity by linking IgG antibody-mediated responses with cellular effector and regulatory functions. Genetic variants in these receptors have been previously identified as risk factors for several chronic inflammatory c...

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Autores principales: Rute B Marques, Mohamed M Thabet, Stefan J White, Jeanine J Houwing-Duistermaat, Aleida M Bakker, Gert-Jan Hendriks, Alexandra Zhernakova, Tom W Huizinga, Annette H van der Helm-van Mil, Rene E Toes
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:e0f2ba3fe0e547aa9bdf99cba5d3a9b52021-11-18T07:03:39ZGenetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.1932-620310.1371/journal.pone.0013173https://doaj.org/article/e0f2ba3fe0e547aa9bdf99cba5d3a9b52010-10-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20957197/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Fc gamma receptors (FcγRs) play a crucial role in immunity by linking IgG antibody-mediated responses with cellular effector and regulatory functions. Genetic variants in these receptors have been previously identified as risk factors for several chronic inflammatory conditions. The present study aimed to investigate the presence of copy number variations (CNVs) in the FCGR3B gene and its potential association with the autoimmune disease rheumatoid arthritis (RA).<h4>Methodology/principal findings</h4>CNV of the FCGR3B gene was studied using Multiplex Ligation Dependent Probe Amplification (MLPA) in 518 Dutch RA patients and 304 healthy controls. Surprisingly, three independent MLPA probes targeting the FCGR3B promoter measured different CNV frequencies, with probe#1 and #2 measuring 0 to 5 gene copies and probe#3 showing little evidence of CNV. Quantitative-PCR correlated with the copy number results from MLPA probe#2, which detected low copy number (1 copy) in 6.7% and high copy number (≥3 copies) in 9.4% of the control population. No significant difference was observed between RA patients and the healthy controls, neither in the low copy nor the high copy number groups (p-values = 0.36 and 0.71, respectively). Sequencing of the FCGR3B promoter region revealed an insertion/deletion (indel) that explained the disparate CNV results of MLPA probe#1. Finally, a non-significant trend was found between the novel -256A>TG indel and RA (40.7% in healthy controls versus 35.9% in RA patients; P = 0.08).<h4>Conclusions/significance</h4>The current study highlights the complexity and poor characterization of the FCGR3B gene sequence, indicating that the design and interpretation of genotyping assays based on specific probe sequences must be performed with caution. Nonetheless, we confirmed the presence of CNV and identified novel polymorphisms in the FCGR3B gene in the Dutch population. Although no association was found between RA and FCGR3B CNV, the possible protective effect of the -256A>TG indel polymorphism must be addressed in larger studies.Rute B MarquesMohamed M ThabetStefan J WhiteJeanine J Houwing-DuistermaatAleida M BakkerGert-Jan HendriksAlexandra ZhernakovaTom W HuizingaAnnette H van der Helm-van MilRene E ToesPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 10 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rute B Marques
Mohamed M Thabet
Stefan J White
Jeanine J Houwing-Duistermaat
Aleida M Bakker
Gert-Jan Hendriks
Alexandra Zhernakova
Tom W Huizinga
Annette H van der Helm-van Mil
Rene E Toes
Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
description <h4>Background</h4>Fc gamma receptors (FcγRs) play a crucial role in immunity by linking IgG antibody-mediated responses with cellular effector and regulatory functions. Genetic variants in these receptors have been previously identified as risk factors for several chronic inflammatory conditions. The present study aimed to investigate the presence of copy number variations (CNVs) in the FCGR3B gene and its potential association with the autoimmune disease rheumatoid arthritis (RA).<h4>Methodology/principal findings</h4>CNV of the FCGR3B gene was studied using Multiplex Ligation Dependent Probe Amplification (MLPA) in 518 Dutch RA patients and 304 healthy controls. Surprisingly, three independent MLPA probes targeting the FCGR3B promoter measured different CNV frequencies, with probe#1 and #2 measuring 0 to 5 gene copies and probe#3 showing little evidence of CNV. Quantitative-PCR correlated with the copy number results from MLPA probe#2, which detected low copy number (1 copy) in 6.7% and high copy number (≥3 copies) in 9.4% of the control population. No significant difference was observed between RA patients and the healthy controls, neither in the low copy nor the high copy number groups (p-values = 0.36 and 0.71, respectively). Sequencing of the FCGR3B promoter region revealed an insertion/deletion (indel) that explained the disparate CNV results of MLPA probe#1. Finally, a non-significant trend was found between the novel -256A>TG indel and RA (40.7% in healthy controls versus 35.9% in RA patients; P = 0.08).<h4>Conclusions/significance</h4>The current study highlights the complexity and poor characterization of the FCGR3B gene sequence, indicating that the design and interpretation of genotyping assays based on specific probe sequences must be performed with caution. Nonetheless, we confirmed the presence of CNV and identified novel polymorphisms in the FCGR3B gene in the Dutch population. Although no association was found between RA and FCGR3B CNV, the possible protective effect of the -256A>TG indel polymorphism must be addressed in larger studies.
format article
author Rute B Marques
Mohamed M Thabet
Stefan J White
Jeanine J Houwing-Duistermaat
Aleida M Bakker
Gert-Jan Hendriks
Alexandra Zhernakova
Tom W Huizinga
Annette H van der Helm-van Mil
Rene E Toes
author_facet Rute B Marques
Mohamed M Thabet
Stefan J White
Jeanine J Houwing-Duistermaat
Aleida M Bakker
Gert-Jan Hendriks
Alexandra Zhernakova
Tom W Huizinga
Annette H van der Helm-van Mil
Rene E Toes
author_sort Rute B Marques
title Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
title_short Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
title_full Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
title_fullStr Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
title_full_unstemmed Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.
title_sort genetic variation of the fc gamma receptor 3b gene and association with rheumatoid arthritis.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/e0f2ba3fe0e547aa9bdf99cba5d3a9b5
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