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PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians
Author(s) -
Gragnoli Claudia
Publication year - 2010
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.21954
Subject(s) - locus (genetics) , haplotype , genetics , linkage disequilibrium , genetic linkage , type 2 diabetes , biology , allele , snp , candidate gene , genetic association , gene , single nucleotide polymorphism , genotype , diabetes mellitus , endocrinology
Type 2 diabetes (T2D) has a replicated linkage on chromosome12q24.2, the non‐insulin‐dependent‐diabetes 2 (NIDDM2) locus. PSMD9 (which rarely causes T2D in Italians) lies in the NIDDM2 region and is implicated in beta cell insulin transcription and diabetes onset in mice. Thus, PSMD9 is a candidate T2D gene for the NIDDM2 locus. We aimed at identifying any linkage of the PSMD9 A/T/G haplotype, or of any of its single variants, to Italian T2D siblings/families. We screened 201 T2D siblings/families for PSMD9 variants and performed a parametric and non‐parametric linkage study, including linkage disequilibrium (LD) modeling and simulation analyses. Our results show a consistent significant LOD score in linkage with T2D for each single PSMD9 SNP variant ( IVS3 + nt460A , P = 3.546E − 007, IVS3 + nt437T , P = 7.723E − 008, and 197G , P = 4.921E − 007) and for the haplotype ( A/T/G for the above‐cited variants, P = 3.078E − 015) using the non‐parametric analysis, as well as the LD modeling test ( P = 4.178E − 009) and the parametric linkage analysis. The strongest signal is present under the recessive model ( P = 4.905E − 011). Our statistical power in the present study relies on the presence of T2D affected siblings, which represent an ideal dataset to identify linkage with a recessive disease model. Our 1,000 simulation analyses, performed for each single test, confirm that the results are not due to random chance. In summary, the A/T/G haplotype in PSMD9 is linked via the recessive allelic model to T2D in Italians. By our observation and testing, the linkage strategy can identify a gene contributing to T2D in a homogeneous subject dataset. J. Cell. Physiol. 222: 265–267, 2010. © 2009 Wiley‐Liss, Inc.