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PTPRD silencing by DNA hypermethylation decreases insulin receptor signaling and leads to type 2 diabetes.

Abstract
Genome-wide association study (GWAS) data showed that the protein tyrosine phosphatase receptor type delta (PTPRD) is associated with increased susceptibility to type 2 diabetes (T2D) in Han Chinese. A replication study indicated that PTPRD is involved in the insulin signaling pathway; however, the underlying mechanism remains unclear. We evaluated PTPRD expression in patients with T2D and controls. PTPRD expression levels were lower in patients and were correlated with the duration of the disease. Overexpression of the human insulin receptor PPARĪ³2 in HepG2 cells induced overexpression of PTPRD and the insulin receptor. PTPRD knockdown, using a shRNA, resulted in down-regulation of the insulin receptor. These results indicate that PTPRD activates PPARĪ³2 in the insulin signaling pathway. Similar results for PTPRD expression were found using a T2D mouse model. Silencing of PTPRD was caused by DNA methylation in T2D mice and patients, and correlated with DNMT1 expression. Furthermore, we showed that a DNMT1 SNP (rs78789647) was correlated with susceptibility to T2D. This study shows for the first time that DNMT1 caused PTPRD DNA hypermethylation and induced insulin signaling silencing in T2D patients. Our findings contribute to a better understanding of the crucial roles of these regulatory elements in human T2D.
AuthorsYng-Tay Chen, Wei-D Lin, Wen-Lin Liao, Ying-Ju Lin, Jan-Gowth Chang, Fuu-Jen Tsai
JournalOncotarget (Oncotarget) Vol. 6 Issue 15 Pg. 12997-3005 (May 30 2015) ISSN: 1949-2553 [Electronic] United States
PMID26079428 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases
  • DNMT1 protein, human
  • Dnmt1 protein, mouse
  • Receptor, IGF Type 1
  • PTPRD protein, human
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2
Topics
  • Animals
  • Case-Control Studies
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases (genetics)
  • DNA Methylation
  • Diabetes Mellitus, Type 2 (blood, enzymology, genetics, metabolism)
  • Female
  • Gene Silencing
  • Genome-Wide Association Study
  • Hep G2 Cells
  • Humans
  • Male
  • Mice
  • Receptor, IGF Type 1 (metabolism)
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2 (genetics, metabolism)
  • Transfection

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