A systems view of epigenetic networks regulating pancreas development and β-cell function

被引:17
|
作者
Xie, Ruiyu
Carrano, Andrea C.
Sander, Maike [1 ]
机构
[1] Univ Calif San Diego, Dept Pediat, Pediat Diabet Res Ctr, Sanford Consortium Regenerat Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
EMBRYONIC STEM-CELLS; DIABETES SUSCEPTIBILITY LOCI; SCALE ASSOCIATION ANALYSIS; DNA METHYLATION; ENDODERM DIFFERENTIATION; INK4A/ARF EXPRESSION; PROVIDES INSIGHTS; IN-VITRO; ISLETS; CHROMATIN;
D O I
10.1002/wsbm.1287
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The development of the pancreas and determination of endocrine cell fate are controlled by a highly complex interplay of signaling events and transcriptional networks. It is now known that an interconnected epigenetic program is also required to drive these processes. Recent studies using genome-wide approaches have implicated epigenetic regulators, such as DNA and histone-modifying enzymes and noncoding RNAs, to play critical roles in pancreas development and the maintenance of cell identity and function. Furthermore, genome-wide analyses have implicated epigenetic changes as a casual factor in the pathogenesis of diabetes. In the future, genomic approaches to further our understanding of the role of epigenetics in endocrine cell development and function will be useful for devising strategies to produce or manipulate beta-cells for therapies of diabetes. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1 / 11
页数:11
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