Sharma, Mamta ; Batra, Jyotsna ; Mabalirajan, Ulaganathan ; Sharma, Shilpy ; Nagarkatti, Rana ; Aich, Jyotirmoi ; Sharma, Surendra K. ; Niphadkar, Pramod V. ; Ghosh, Balaram (2008) A genetic variation in inositol polyphosphate 4 phosphatase A enhances susceptibility to asthma American Journal of Respiratory and Critical Care Medicine, 177 . pp. 712-719. ISSN 1073-449X
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Official URL: http://ajrccm.atsjournals.org/cgi/content/abstract...
Related URL: http://dx.doi.org/10.1164/rccm.200705-781OC
Abstract
Rationale: Microarray data from mouse studies have identified a number of genes to be differentially expressed in allergen-sensitized mice lungs. Objectives: Taking leads from these datasets, we attempted to identify novel genes associated with atopic asthma in humans. Methods: We performed family-based genetic association analysis on selected markers within or in proximity of 21 human homologs of genes short-listed from ovalbumin-sensitized mouse studies in the Gene Expression Omnibus database of the National Center for Biotechnology Information. Family-based and case-control studies were undertaken for fine mapping and functional variation analysis of INPP4A (inositol polyphosphate 4 phosphatase type I). Western blot analysis was performed to analyze INPP4A protein stability from human platelets. Measurements and Main Results: Our genetic association studies of 21 human genes in 171 trios led to the identification of a biallelic repeat (rs3217304) in INPP4A, associated with atopic asthma (P = 0.009). Further studies using additional three single nucleotide polymorphisms (SNPs), +92031A/T, +92344C/T, and +131237C/T, and two microsatellite markers, D2S2311 and D2S2187, revealed significant genetic associations with loci +92031A/T (P = 0.0012) and +92344C/T (P = 0.004). A nonsynonymous SNP, +110832A/G (Thr/Ala), present within a sequence enriched with proline, glutamic acid, serine, and threonine (PEST), in proximity of these two loci, showed a significant association with atopic asthma (P = 0.0006). The association results were also replicated in an independent cohort of 288 patients and 293 control subjects (P = 0.004). PEST score and Western blot analyses indicated a functional role of this SNP in regulating INPP4A protein stability. Conclusions: In our study, INPP4A was identified as a novel asthma candidate gene, whereby the +110832A/G (Thr/Ala) variant affected its stability and was significantly associated with asthma.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Thoracic Society. |
Keywords: | Asthma; Gene; INPP4A; Single Nucleotide Polymorphism |
ID Code: | 66031 |
Deposited On: | 21 Oct 2011 03:34 |
Last Modified: | 21 Oct 2011 03:34 |
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