Northampton Electronic Collection of Theses and Research

A comparison of assays for accurate copy number measurement of the low-affinity Fc gamma receptor genes FCGR3A and FCGR3B

Haridan, U. S., Mokhtar, U., Machado, L., Abdul Aziz, A. T., Shueb, R. H., Zaid, M., Sim, B., Mustafa, M., Nik Yusof, N. K., Lee, C. K. C., Abu Bakar, S., AbuBakar, S., Hollox, E. J. and Boon Peng, H. (2015) A comparison of assays for accurate copy number measurement of the low-affinity Fc gamma receptor genes FCGR3A and FCGR3B. PLoS ONE. 10(1) 1932-6203.

Item Type: Article
Abstract: The FCGR3 locus encoding the low affinity activating receptor FcγRIII, plays a vital role in immunity triggered by cellular effector and regulatory functions. Copy number of the genes FCGR3A and FCGR3B has previously been reported to affect susceptibility to several autoimmune diseases and chronic inflammatory conditions. However, such genetic association studies often yield inconsistent results; hence require assays that are robust with low error rate. We investigated the accuracy and efficiency in estimating FCGR3 CNV by comparing Sequenom MassARRAY and paralogue ratio test-restriction enzyme digest variant ratio (RT-REDVR). In addition, since many genetic association studies of FCGR3B CNV were carried out using real-time quantitative PCR, we have also included the evaluation of that method’s performance in estimating the multi-allelic CNV of FCGR3B. The qPCR assay exhibited a considerably broader distribution of signal intensity, potentially introducing error in estimation of copy number and higher false positive rates. Both Sequenom and PRT-REDVR showed lesser systematic bias, but Sequenom skewed towards copy number normal (CN = 2). The discrepancy between Sequenom and PRT-REDVR might be attributed either to batch effects noise in individual measurements. Our study suggests that PRT-REDVR is more robust and accurate in genotyping the CNV of FCGR3, but highlights the needs of multiple independent assays for extensive validation when performing a genetic association study with multi-allelic CNVs.
Subjects: Q Science > QR Microbiology > QR180 Immunology
Q Science > QH Natural history > QH426 Genetics > QH438.7 Human genetics
Creators: Haridan, Umi Shakina, Mokhtar, Umairah, Machado, Lee, Abdul Aziz, Abu Thalhah, Shueb, Rafidah Hanim, Zaid, Masliza, Sim, Benedict, Mustafa, Mahiran, Nik Yusof, Nik Khairudin, Lee, Christopher K C, Abu Bakar, Suhaili, AbuBakar, Sazaly, Hollox, Edward J and Boon Peng, Hoh
Publisher: Public Library of Science
Northamptonshire and East Midlands: Health
Faculties, Divisions and Institutes: University Faculties, Divisions and Research Centres - OLD > Faculty of Health & Society > Sports, Exercise & Life Sciences
University Faculties, Divisions and Research Centres - OLD > Research Centre > Institute of Health and Wellbeing > Ageing Research Centre
Faculties > Faculty of Health & Society > Sports, Exercise & Life Sciences
Research Centres > Centre for Health Sciences and Services
Research Centres > Centre for Physical Activity and Life Sciences
Date: 16 January 2015
Date Type: Publication
Journal or Publication Title: PLoS ONE
Volume: 10
Number: 1
Language: English
DOI: https://doi.org/10.1371/journal.pone.0116791
ISSN: 1932-6203
Status: Published / Disseminated
URI: http://nectar.northampton.ac.uk/id/eprint/7304

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