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A fast and easy real-time PCR genotyping method for the HLA-G 14-bp insertion/deletion polymorphism in the 3' untranslated region.

Authors :
Djurisic S
Sørensen AE
Hviid TV
Source :
Tissue antigens [Tissue Antigens] 2012 Mar; Vol. 79 (3), pp. 186-9. Date of Electronic Publication: 2012 Jan 06.
Publication Year :
2012

Abstract

Human leukocyte antigen-G (HLA-G) is a non-classical HLA class Ib molecule shown to exhibit immunomodulatory function in a wide range of immune-based disorders. A number of functional HLA-G gene polymorphisms have been identified, including a 14-bp insertion/deletion polymorphism in exon 8 of the 3' untranslated region of the HLA-G gene, which has been associated with HLA-G mRNA stability. Moreover, studies show that homozygosity for the 14-bp insertion/deletion polymorphism is associated with lower HLA-G mRNA and protein levels and unique alternative splicing patterns. Here, we introduce a quick and reliable method to screen for the HLA-G 14-bp insertion/deletion polymorphism using an optimized real-time polymerase chain reaction protocol. The genotyping assay has been validated by comparison with conventional methods. As results can be obtained within a few hours, the assay will have a potential for clinical use.<br /> (© 2012 John Wiley & Sons A/S.)

Details

Language :
English
ISSN :
1399-0039
Volume :
79
Issue :
3
Database :
MEDLINE
Journal :
Tissue antigens
Publication Type :
Academic Journal
Accession number :
22220924
Full Text :
https://doi.org/10.1111/j.1399-0039.2011.01830.x