Association of AluYb8 insertion/deletion polymorphism in the MUTYH gene with mtDNA maintain in the type 2 diabetes mellitus patients.

Abstract

A common AluYb8-element insertion/deletion polymorphism of the MUTYH gene (AluYb8MUTYH) is a novel genetic risk factor for type 2 diabetes mellitus (T2DM). In the present study, mtDNA sequencing analysis indicated that the mtDNA sequence heteroplasmy was not associated with AluYb8MUTYH polymorphism. To better understand the genetic risk for T2DM, we investigated the association of this polymorphism with mtDNA content, mtDNA breakage and mtDNA transcription in the leukocytes of T2DM patients. The mtDNA content and unbroken mtDNA were significantly increased in the mutant patients than in the wild-type patients (P <0.05, respectively). However, no association between mtDNA transcription and AluYb8MUTYH variant was observed. The results suggested that the AluYb8MUTYH variant was associated with an altered mtDNA maintain in T2DM patients. The high level of mtDNA content observed in the mutant patients may have resulted from inefficient base excision repair of mitochondrial MUTYH and a compensatory mechanism that is triggered by elevated oxidative stress.

• Authors: Wenwen Guo, Bixia Zheng, Dong Guo, Zhenming Cai, Yaping Wang
• Journal: Molecular and cellular endocrinology (Mol Cell Endocrinol) Vol. 409 Pg. 33-40 (Jul 05 2015) ISSN: 1872-8057 [Electronic] Ireland
• PMID: 25829257 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Chemical References

• DNA, Mitochondrial
• DNA Glycosylases
• mutY adenine glycosylase

Topics

• Adult
• Aged
• Alu Elements
• DNA Glycosylases (genetics)
• DNA, Mitochondrial (genetics)
• Diabetes Mellitus, Type 2 (blood, genetics)
• Female
• Genetic Association Studies
• Humans
• INDEL Mutation
• Male
• Middle Aged
• Polymorphism, Genetic
• Sequence Analysis, DNA
• Transcription, Genetic
• Young Adult