Epigenetic changes in diabetes

被引:67
|
作者
Keating, S. T. [1 ]
El-Osta, A. [1 ,2 ,3 ,4 ]
机构
[1] Alfred Med Res & Educ Precinct, Epigenet Human Hlth & Dis Lab, Melbourne, Vic 3004, Australia
[2] Alfred Med Res & Educ Precinct, Baker IDI Heart & Diabet Inst, Epigen Profiling Facil, Melbourne, Vic 3004, Australia
[3] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
[4] Monash Univ, Cent Clin Sch, Dept Med, Melbourne, Vic 3800, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
chromatin; complications; diabetes; epigenetic; histones; metabolic memory; methylation; INTRAUTERINE GROWTH-RETARDATION; SMOOTH-MUSCLE-CELLS; DNA METHYLATION; CHROMATIN-STRUCTURE; METABOLIC MEMORY; GENE-EXPRESSION; HIGH GLUCOSE; HISTONE ACETYLATION; CRYSTAL-STRUCTURE; GLYCEMIC CONTROL;
D O I
10.1111/cge.12121
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Diabetes is a multifactorial disease with numerous pathways influencing its progression and recent observations suggest that the complexity of the disease cannot be entirely accounted for by genetic predisposition. A compelling argument for an epigenetic component is rapidly emerging. Epigenetic processes at the chromatin template significantly sensitize transcriptional and phenotypic outcomes to environmental signaling information including metabolic state, nutritional requirements and history. Epigenetic mechanisms impact gene expression that could predispose individuals to the diabetic phenotype during intrauterine and early postnatal development, as well as throughout adult life. Furthermore, epigenetic changes could account for the accelerated rates of chronic and persistent microvascular and macrovascular complications associated with diabetes. Epidemiological and experimental animal studies identified poor glycemic control as a major contributor to the development of diabetic complications and highlight the requirement for early intervention. Early exposure to hyperglycemia can drive the development of complications that manifest late in the progression of the disease and persist despite improved glycemic control, indicating a memory of the metabolic insult. Understanding the molecular events that underlie these transcriptional changes will significantly contribute to novel therapeutic interventions to prevent, reverse or retard the deleterious effects of the diabetic milieu.
引用
收藏
页码:1 / 10
页数:10
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